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 Table of Contents  
Year : 2018  |  Volume : 10  |  Issue : 2  |  Page : 51-60  

Alopecia areata: Review of epidemiology, clinical features, pathogenesis, and new treatment options

1 Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Fl 33136, USA
2 Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, Miami, Fl 33136, USA

Date of Web Publication23-Apr-2018

Correspondence Address:
Evan Darwin
Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, 1600 NW 10th Ave., RMSB 2023, Miami, Fl 33136
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/ijt.ijt_99_17

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Alopecia areata (AA) is a complex autoimmune condition that causes nonscarring hair loss. It typically presents with sharply demarcated round patches of hair loss and may present at any age. In this article, we review the epidemiology, clinical features, pathogenesis, and new treatment options of AA, with a focus on the immunologic mechanism underlying the treatment. While traditional treatment options such as corticosteroids are moderately effective, a better understanding of the disease pathogenesis may lead to the development of new treatments that are more directed and effective against AA. Sources were gathered from PubMed, Embase, and the Cochrane database using the keywords: alopecia, alopecia areata, hair loss, trichoscopy, treatments, pathogenesis, and epidemiology.

Keywords: Alopecia, alopecia areata, alopecia totalis, alopecia universalis, hair loss

How to cite this article:
Darwin E, Hirt PA, Fertig R, Doliner B, Delcanto G, Jimenez JJ. Alopecia areata: Review of epidemiology, clinical features, pathogenesis, and new treatment options. Int J Trichol 2018;10:51-60

How to cite this URL:
Darwin E, Hirt PA, Fertig R, Doliner B, Delcanto G, Jimenez JJ. Alopecia areata: Review of epidemiology, clinical features, pathogenesis, and new treatment options. Int J Trichol [serial online] 2018 [cited 2023 May 30];10:51-60. Available from: https://www.ijtrichology.com/text.asp?2018/10/2/51/230825

   Methods Top

Articles were gathered from PubMed, Cochrane Reviews, and Embase using the following keywords: Alopecia, alopecia areata, hair loss, trichoscopy, treatments, epidemiology, and pathogenesis. Articles were selected for their relevance and innovative perspective related to the epidemiology, clinical features, pathogenesis, and treatment of alopecia areata (AA).

   Epidemiology Top

AA is an autoimmune condition that attacks the hair follicles, causing nonscarring hair loss. Population studies from the Rochester Epidemiology Project estimate a lifetime incidence of AA of 2.1%, in a population in Olmsted County, Minnesota, with no difference in incidence between genders.[1] A systemic review of the epidemiology of AA indicated a similar worldwide lifetime incidence of around 2%.[2] Some smaller studies indicate a slight female-to-male gender bias, but this may be due to higher female concern regarding hair loss and subsequent treatment.[3] The disorder can occur at any age and the lifetime incidence appears to increase at an almost linear rate.[1] The median age at diagnosis is 33.[1] Male patients may be more likely to be diagnosed in childhood, while females are more likely to present in adolescence and have greater concomitant nail involvement or concomitant autoimmune diseases.[3]

   Clinical Features Top

AA typically presents as smooth, sharply demarcated, round patches of hair loss without atrophy [Figure 1] with “exclamation point hairs” [Figure 2] observed on the periphery of the patches.[4] Special designations of the disease include alopecia universalis (AU) (total body hair loss), alopecia totalis (AT) (total scalp hair loss) [Figure 3], or alopecia in an ophiasis pattern (band-like hair loss on the temporal and occipital scalp) [Figure 4].[4] Less common variants include the diffuse variant with widespread thinning of hair across the scalp or the reticular pattern with recurrent hair loss in one area and spontaneous hair regrowth in another.[4] Ophiasis inversus causes band-like hair loss in the frontoparietotemporal area.[4]
Figure 1: Patchy alopecia areata

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Figure 2: Exclamation point hairs are thicker at the apex of the hair shaft and progressively thin toward the base of the hair shaft

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Figure 3: Alopecia totalis

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Figure 4: Alopecia in an ophiasis pattern

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Nail abnormalities are associated with the disease with an incidence estimated between 7% and 66%.[5] Most frequently, nail pitting is observed, although AA is also associated with trachyonychia, Beau's lines, onychorrhexis, nail thinning or thickening, onychomadesis, punctate or transverse leukonychia, red spot lunulae, and koilonychias.[4] Other commonly associated conditions are thyroid disease (8%–28%),[6] vitiligo (1.8–16%),[6],[7] and atopy (1%–52%).[6]

Other skin conditions that may be confused with AA include traction alopecia, temporal triangular alopecia, androgenic alopecia, trichotillomania, tinea capitis, secondary syphilis, pressure-related alopecia, aplasia cutis, chemotherapy-induced alopecia, telogen effluvium, and the many forms of cicatricial alopecia.[8],[9]

   Prognosis Top

The prognosis of the disease is unpredictable. Current data suggest 34%–50% of patients recover within 1 year, while 14%–25% of patients will progress to AT or AU, at which point patients rarely fully recover.[10],[11] In a retrospective chart review in patients with AU/AT during 10 years, it was found that 12 out of 70 patients with AT/AU (17.1%) had complete hair regrowth.[12] Seventeen out of 70 patients with AT/AU (24.2%) reported hair regrowth ≥90%.[12] Thirty patients with AU (65.2%) had no improvement, and five patients with AT (20.8%) showed no hair regrowth.[12] Patients may have several incidents of hair loss and subsequent regrowth throughout their lives. Family history of AA, young age at onset, nail dystrophy, extensive hair loss, ophiasis, a history of atopy, or the presence of other autoimmune diseases are associated with a poor prognosis.[13]

   Diagnosis Top

The diagnosis is typically clinical and may be aided by findings such as a positive hair pull test or trichoscopy. On trichoscopy, active disease is characterized by yellow dots, black dots, “exclamation mark” or tapering hairs, and broken hairs. Vellus hair in lesions is another marker of AA and may indicate late or inactive disease.[9],[14] Biopsy may be taken in uncertain cases.

   Histopathology Top

The histopathology of the disease will vary per the disease stage. In the acute and subacute stages, there is a peribulbar lymphocytic infiltrate in a “swarm of bees” pattern composed of CD4+ and CD8+ T-cells around anagen follicles [Figure 5].[15],[16] In addition, there is a shift from the catagen hair growth stage to the telogen phase (resting phase), with follicle miniaturization.[15] Edema, microvesiculation, apoptosis, macrophages, and foreign body giant cells may be seen around the hair follicles. In the chronic stage, the inflammation may or may not resolve, but the number of catagen or telogen hairs increases, and there is pigmentary incontinence.[15] In the recovery stage, there is minimal inflammation and anagen hair (actively growing hair) count increases.[16]
Figure 5: “Swarm of bees” pattern of lymphocytes surrounding the hair follicle

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   Pathophysiology Top

The exact pathophysiology of the disease is currently unknown. However, evidence suggests that AA is caused by an autoimmune reaction to the hair follicles due to both genetic and environmental factors.[16] Animal models used for treatment and pathophysiologic mechanisms are summarized in [Table 1].
Table 1: Current murine models used in alopecia areata

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Genetic factors

Observational studies show a high correlation (10%–42%) between AA and family history.[26],[27] Genome-wide association studies have identified numerous single-nucleotide polymorphisms (SNPs) associated with AA. In a recent meta-analysis, human leukocyte antigen-DR (HLA-DR) on chromosome 6 appears to be the largest risk factor for AA.[28] These HLA class II genes are highly linked to CD4+ and CD8+ T-cells, which are important effector cells in AA.[28] In addition, this study implicated BCL2-like protein 11, also known as BIM, which helps to regulate autophagy in the disease pathogenesis.[28] Genes encoding for natural killer cell receptor D ligands and downstream effectors of the JAK pathway also influence AA susceptibility.[29],[30] Other implicated pathways include T-regulatory cells (Tregs), autophagy, and apoptosis, although more information is needed to determine the exact mechanisms.[28]

Environmental factors

Environmental factors likely exacerbate or induce AA. Stress is an often-cited cause of AA, but the literature from human studies is inconclusive.[31],[32],[33] However, in a mouse model, the activity of the central and peripheral hypothalamus pituitary adrenal axis was higher compared to normal mice. The elevated adrenocorticotropic hormone, corticosterone, and estradiol correlated to elevated pro-inflammatory cytokine levels in the skin, suggesting a potential role of psychological and physiological stressors to cause AA.[34] Other potential environmental stressors that may be implicated in AA include infections,[35] vaccinations, hormone fluctuations, and diet, although their exact impact is unknown.[16],[36] In the mouse model, soy products have been associated with AA, and there are new studies emphasizing a correlation between AA and Vitamins A and D levels.[16],[37] It is likely that multiple environmental factors impact the disease course.

Immune privilege zone

In the normal hair follicle, there is a zone of immune privilege due to downregulation of MHC I and β2 macroglobulin molecules, production of immunosuppressant molecules such as α-melanocyte-stimulating hormone and transforming growth factor-β (TNF-β) and decreased antigen-presenting cell activity.[38],[39] However, it is hypothesized that there is a collapse of this immune privilege zone in AA from an unknown autoantigen.[38] Interferon-γ (IFN-γ) and interleukin (IL)-2 can then induce infiltration of CD8+, CD4+, and other inflammatory cells into the immune privilege zone.[36] All of these alterations are translated in inflammation of the hair follicle and may result in hair loss.[40]

   Current Treatments Top

Few high-quality randomized controlled trials have been completed for the management of AA, although this has begun to change with the addition of the Severity of Alopecia Tool which provides guidelines for clinical research in AA.[41] Hair loss may spontaneously remit, although the timeframe for regrowth may be months to years.[42] Traditional medical therapies include corticosteroids, immunotherapy, and light therapy.[42],[43]

Topical corticosteroids

The underlying mechanism of topical corticosteroid use is containment of inflammation and hastening of the recovery of damaged hair follicles.[42],[44] Results vary, but approximately 57% of patients demonstrate complete regrowth of hair during the course of treatment.[44] Intralesional corticosteroids show slightly better results, with 63% demonstrating complete hair regrowth within 4 months in one study.[45] The main side effect is increased risk of cutaneous atrophy at the site of treatment.[42] Systemic corticosteroids are used in refractory cases, with one study demonstrating that 62% of patients had full hair regrowth.[46] However, the therapy may be associated with adverse events.[46],[47] Relapse rates in AA are high regardless of therapy, and with corticosteroids vary between 33% and 75%.[48]


Squaric acid dibutylester and diphencyclopropenone are immunotherapeutic agents used as the second-line treatments for AA. The postulated mechanism is induction of antigenic competition which distracts CD4+ T-cells from attacking hair follicles.[49] Urticaria, dermatitis, blistering, and depigmentation are common side effects.[42] Response rates vary from 9% to 87%, but one study showed that 20%–30% of patients get a response sufficient to avoid the need for a hair piece.[42]

Other less commonly used treatments include topical minoxidil,[50] plus ultraviolet A radiation or excimer laser,[43],[51] and systemic immunomodulators.[43]

   Investigational Treatments and Future Directions Top


Tregs are impaired in autoimmune diseases such as AA.[52],[53] Low dose IL-2 is known to induce Treg proliferation, which might reduce the immune response against hair follicles.[53],[54] A pilot study of IL-2 for 6 months of treatment indicated that low-dose treatment can improve AU with minimal adverse events.[52] Biopsy of lesions demonstrated a decrease in CD8+ T-cells and an increase in Tregs.[52] However, IL-2 may also have a paradoxical effect, increasing NK cell proliferation, and potentially exacerbating AA.[53]

Interleukin 17

IL-17 SNPs are associated with AA, and TH17 cells are increased around hair cells in AA.[55],[56] IL-17 activation can increase inflammatory cytokines such as TNF-β, IL-6, and IFN-γ.[56],[57] It is postulated that therapy to limit TH17 cells would inhibit IL-17, and therefore help to treat AA.[56] However, there have been no clinical trials to date.


Many contact allergens have been studied for the treatment of AA.[58] Phenol (carbolic acid) is a contact irritant, which acts as an immunomodulative drug and through “antigenic competition” decreases the immune response against the hair follicle.[58] Savant and Shenoy documented a response to 88% phenol in 69 patches of AA but did not reported specific changes regarding pigmentation, density, and texture of hair regrowth.[59] Chikhalkar et al. in 2011 performed a prospective study using 88% phenol topically on AA patches and found a 78% improvement regarding texture and pigmentation of hair.[58]


Quercetin is an anti-inflammatory bioflavonoid that has been tested in mice to treat AA.[60] Previous studies have shown that it can inhibit Heat Shock Protein 70 and nuclear factor-kappa B transcription factors that activate inflammatory cytokines such as TNF-β, IL-1, IL-2, and IL-6.[60] In Wikramanayake et al., all mice treated with quercetin demonstrated hair regrowth, whereas none of the sham-treated mice showed any hair regrowth.[60] In addition, 24% of the heat-treated mice (a method to induce AA) with sham-injections developed AA, while none of the mice receiving quercetin developed the disease.[60]


Tianeptine is an antidepressant sold outside the US that acts as an opioid agonist and serotonin reuptake enhancer. In one animal study, tianeptine was given to mice with ultrasonic wave stress-induced AA-like lesions.[61] At the end of the study, treated mice demonstrated reduced hair loss, regrowth, improved hair thickness, and increased hair-cycle recovery.[61] There was also decreased mast cell degranulation surrounding hair follicles and increased synthesis of collagen and elastic fibers.[61] Small clinical trials have demonstrated some hair regrowth with imipramine [62] and paroxetine,[63] although no trial has demonstrated complete regrowth.

Parathyroid hormone

Parathyroid hormone (PTH) is thought to be a hair cycle stimulator.[64] It has been tested on the C3H/HEJ mouse model of AA with promising results.[64] Forty mice were treated with either PTH bound to a bacterial collagen binding domain (PTH-CBD) or a control.[64] Eight weeks after treatment, 13/21 mice (62%) treated with PTH-CBD showed reduced hair loss, while only 3/10 (30%) in the control group demonstrated retained hair.[64] There was no change in immune response on immunohistochemistry, but increased anagen hair follicles and increased beta-catenin (anagen hair growth initiator) were noted.[64]

Low-level light therapy

Low-level light therapy (LLLT) has primarily been used for androgenic alopecia, but there are some studies examining its use for AA. The Hairmax Lasercomb® (Boca Raton, Florida, USA) was used to treat heat-induced AA in C3H/HeJ mice. At the end of the trial, the laser-treated mice had increased hair regrowth and increased hair follicles in the anagen phase on histology in comparison to the sham control.[65] However, in a similar study with spontaneous or graft-induced AA in C3H/HeJ mice, there was no increase in hair regrowth.[66] The authors postulate this may be due to a difference between heat-induced AA and spontaneous AA.[66] In a solitary trial with a pulsed infrared diode 904 nm laser, 32 of 34 treated patches demonstrated hair regrowth without any adverse events.[67] However, this pulsed laser treatment may affect the body differently than the more constant light of traditional LLLT devices such as the Hairmax Lasercomb®.


CTLA-4 is a receptor present in the surface of immune cells that through its signaling pathways is believed to be a critical regulator of AA onset and maintenance.[68] Sundberg et al. in 1994 performed a comparative human gene array to identify dysregulated genes in AA.[69] One of the genes studied was CTLA-4, a co-stimulatory T-cell ligand that binds B7.1 (CD80) and B7.2 (CD86) on antigen-presenting cells.[68] Abatacept, a monoclonal antibody directed against this receptor, effectively prevented the onset of AA in a mouse model.[17],[20] Recently, John et al. defined CTLA-4 as a major candidate gene for AA susceptibility in humans.[70] Abatacept as an immunosuppressive drug is used to treat many rheumatologic treatments and acts on the CTLA-4 pathway.[71] Due to many adverse effects, it should be used cautiously.

JAK inhibitors

JAK inhibitors have been approved to treat diseases such as rheumatoid arthritis and myelofibrosis. Oral and topical JAK inhibitor treatments have both prevented and reversed AA in mouse models. It is thought that JAK inhibitors act by preventing the upregulation of IFN-γ that is necessary for the immune response of AA.[72] No randomized controlled studies have been completed yet, but there have been several case series and reports demonstrating hair regrowth in patients with AA and AU.[73],[74],[75] Many clinical trials are ongoing involving JAK inhibitors such as ruxolitinib, tofacitinib, and baricitinib [Table 2].
Table 2: Ongoing interventional clinical trials related to alopecia areataa

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Platelet-rich plasma

Platelet-rich plasma (PRP) is thought to initiate wound healing through secretion of various growth factors and cytokines. It has recently been used to treat AA. In mice, PRP has been shown to prolong the anagen phase through increases in B-catenin and fibroblast growth factor-7 and also has an antiapoptotic effect on dermal papilla cells.[76] In randomized studies, PRP demonstrated significantly improved hair regrowth compared to placebo and triamcinolone scalp injections without any noted adverse events.[77] However, in another trial in chronic severe AA, there was a variable effect with PRP treatment.[78] A recent trial comparing PRP, topical minoxidil, and placebo showed both significantly increased hair regrowth with PRP compared to placebo and significantly earlier response than topical minoxidil.[50] More randomized studies will be necessary to determine the comparable efficacy of this treatment to standard therapy.


Statins have anti-inflammatory and immunomodulatory effects that may improve hair regrowth.[79] Statins are theorized to affect hair regrowth by inhibiting STAT phosphorylation that activates several important inflammatory cytokines and also by altering the balance of Th1/Th2, suppressing IL-17, decreasing mast cell degranulation, and inhibiting lymphocyte migration.[80],[81] The clinical trial data are conflicting. In one trial, 19 patients with 40–70% hair loss completed the treatment, and 14 patients were considered responders to treatment.[79] However, in another study in patients with 70% or greater hair loss or AU/AT treated with simvastatin, there was no demonstrated hair regrowth.[82] It is unclear if the lack of response in this later trial was due to the increased severity of the disease or if the therapy was ineffective. Larger randomized controlled clinical trials should be conducted for further evaluation.

Vitamin A

Immune cells are highly responsive to oxidative damage.[83] Provitamin A and β-carotene have well-known antioxidant properties, and vitamin A itself has physiologic roles in immune modulation.[84] Deficiency or excess in vitamin A can result in AA. Duncan et al. documented an upregulation of genes that play a role in retinoid metabolism in AA patch biopsies from humans and mouse model C3H/HeJ.[85] Mice fed with high levels of vitamin A presented earlier with the disease.[85] Suo et al. confirmed a role for vitamin A in the initiation of the anagen hair cycle in C3H/HeJ mice, which likely increases follicle susceptibility to autoimmune destruction and it was dose-dependent.[86]

Valproic acid

Valproic acid (VPA) is a mood stabilizer. VPA affects signaling pathways including protein kinase C, extracellular signal-regulated kinase, and Wnt/β-catenin pathways.[87],[88] Lee et al. in 2012 performed topical application of VPA to male C3H mice and found that it stimulated hair regrowth and induced terminally differentiated epidermal markers such as filaggrin and loricrin, and the dermal papilla marker alkaline phosphatase.[89] More research has to be done to prove its effectiveness in humans.


Microneedling is a new procedure performed by superficial puncturing of the skin by rolling with miniature needles. Traditionally, it has been used as a collagen induction therapy for scars and skin rejuvenation; and as a transdermal delivery system for therapeutic drugs and vaccines [90] and recently in androgenic alopecia.[91] Microneedling has also been combined with topical triamcinolone acetonide application in AA.[92] Ito et al. in 2017 used a three microneedle device for intralesional corticosteroid administration in patients with AA with beneficial results.[93] Deepak et al. in 2014 also reported positive results in three cases of resistant AA treated with scalp roller therapy.[94]


Electroacupuncture (EA) involves insertion of needles into the skin and underlying tissues at acupuncture points with pulsating electrical current.[18] Evidence has indicated that EA stimulation may enhance immune function in several animal models of inflammatory diseases.[18] Maeda et al., applied EA stimulation at the ST36 point in C3H/HeJ mice with AA, and found a significant reduction of mast cell degranulation around hair follicles, improving AA.[18]

   Conclusion Top

AA is a complicated multifactorial disease with a variable prognosis. While many patients will heal spontaneously, other patients may have chronic disease. There are no FDA approved treatments, although corticosteroids are considered first line. Potential new avenues of therapy have been explored here and will require more extensive review before their use can be recommended [Table 2] and [Table 3]. Further research into the mechanism of the disease may also elucidate further treatment options.
Table 3: Investigational treatment options for alopecia areata

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Thank you to Dr. Mariya Miteva MD Assistant Professor at the University of Miami Miller School of Medicine Department of Dermatology and Cutaneous Surgery for providing the photographs and histologic images used in this manuscript.

Financial support and sponsorship


Conflicts of interest

There are no conflicts of interest.

   References Top

Mirzoyev SA, Schrum AG, Davis MD, Torgerson RR. Lifetime incidence risk of alopecia areata estimated at 2.1% by Rochester epidemiology project, 1990-2009. J Invest Dermatol 2014;134:1141-2.  Back to cited text no. 1
Villasante Fricke AC, Miteva M. Epidemiology and burden of alopecia areata: A systematic review. Clin Cosmet Investig Dermatol 2015;8:397-403.  Back to cited text no. 2
Lundin M, Chawa S, Sachdev A, Bhanusali D, Seiffert-Sinha K, Sinha AA, et al. Gender differences in alopecia areata. J Drugs Dermatol 2014;13:409-13.  Back to cited text no. 3
Alkhalifah A. Alopecia areata update. Dermatol Clin 2013;31:93-108.  Back to cited text no. 4
Gandhi V, Baruah MC, Bhattacharaya SN. Nail changes in alopecia areata: Incidence and pattern. Indian J Dermatol Venereol Leprol 2003;69:114-5.  Back to cited text no. 5
[PUBMED]  [Full text]  
Goh C, Finkel M, Christos PJ, Sinha AA. Profile of 513 patients with alopecia areata: Associations of disease subtypes with atopy, autoimmune disease and positive family history. J Eur Acad Dermatol Venereol 2006;20:1055-60.  Back to cited text no. 6
Hordinsky M, Ericson M. Autoimmunity: Alopecia areata. J Investig Dermatol Symp Proc 2004;9:73-8.  Back to cited text no. 7
Mubki T, Rudnicka L, Olszewska M, Shapiro J. Evaluation and diagnosis of the hair loss patient: Part I. History and clinical examination. J Am Acad Dermatol 2014;71:415.e1-415.e15.  Back to cited text no. 8
Mubki T, Rudnicka L, Olszewska M, Shapiro J. Evaluation and diagnosis of the hair loss patient: Part II. Trichoscopic and laboratory evaluations. J Am Acad Dermatol 2014;71:431.e1-431.e11.  Back to cited text no. 9
Tosti A, Bellavista S, Iorizzo M. Alopecia areata: A long term follow-up study of 191 patients. J Am Acad Dermatol 2006;55:438-41.  Back to cited text no. 10
Gip L, Lodin A, Molin L. Alopecia areata. A follow-up investigation of outpatient material. Acta Derm Venereol 1969;49:180-8.  Back to cited text no. 11
Jang YH, Hong NS, Moon SY, Eun DH, Lee WK, Chi SG, et al. Long-term prognosis of alopecia totalis and alopecia universalis: A Longitudinal study with more than 10 years of follow-up: Better than reported. Dermatology 2017;233:250-6.  Back to cited text no. 12
Madani S, Shapiro J. Alopecia areata update. J Am Acad Dermatol 2000;42:549-66.  Back to cited text no. 13
Mane M, Nath AK, Thappa DM. Utility of dermoscopy in alopecia areata. Indian J Dermatol 2011;56:407-11.  Back to cited text no. 14
[PUBMED]  [Full text]  
Yoon TY, Lee DY, Kim YJ, Lee JY, Kim MK. Diagnostic usefulness of a peribulbar eosinophilic infiltrate in alopecia areata. JAMA Dermatol 2014;150:952-6.  Back to cited text no. 15
Alkhalifah A, Alsantali A, Wang E, McElwee KJ, Shapiro J. Alopecia areata update: Part I. Clinical picture, histopathology, and pathogenesis. J Am Acad Dermatol 2010;62:177-88.  Back to cited text no. 16
Carroll JM, McElwee KJ, King LE, Byrne MC, Sundberg JP. Gene array profiling and immunomodulation studies define a cell-mediated immune response underlying the pathogenesis of alopecia areata in a mouse model and humans. J Invest Dermatol 2002;119:392-402.  Back to cited text no. 17
Maeda T, Taniguchi M, Matsuzaki S, Shingaki K, Kanazawa S, Miyata S, et al. Anti-inflammatory effect of electroacupuncture in the C3H/HeJ mouse model of alopecia areata. Acupunct Med 2013;31:117-9.  Back to cited text no. 18
Silva KA, Sundberg JP. Surgical methods for full-thickness skin grafts to induce alopecia areata in C3H/HeJ mice. Comp Med 2013;63:392-7.  Back to cited text no. 19
Sun J, Silva KA, McElwee KJ, King LE Jr., Sundberg JP. The C3H/HeJ mouse and DEBR rat models for alopecia areata: Review of preclinical drug screening approaches and results. Exp Dermatol 2008;17:793-805.  Back to cited text no. 20
Wikramanayake TC, Alvarez-Connelly E, Simon J, Mauro LM, Guzman J, Elgart G, et al. Heat treatment increases the incidence of alopecia areata in the C3H/HeJ mouse model. Cell Stress Chaperones 2010;15:985-91.  Back to cited text no. 21
Alli R, Nguyen P, Boyd K, Sundberg JP, Geiger TL. A mouse model of clonal CD8+ T lymphocyte-mediated alopecia areata progressing to alopecia universalis. J Immunol 2012;188:477-86.  Back to cited text no. 22
Gu ME, Song XM, Zhu CF, Yin HP, Liu GJ, Yu LP, et al. Breeding and preliminarily phenotyping of a congenic mouse model with alopecia areata. Dongwuxue Yanjiu 2014;35:249-55.  Back to cited text no. 23
Sundberg JP, Berndt A, Silva KA, Kennedy VE, Sundberg BA, Everts HB, et al. Alopecia areata: Updates from the mouse perspective. J Investig Dermatol Symp Proc 2013;16:S23-4.  Back to cited text no. 24
Gilhar A, Keren A, Paus R. A new humanized mouse model for alopecia areata. J Investig Dermatol Symp Proc 2013;16:S37-8.  Back to cited text no. 25
McDonagh AJ, Tazi-Ahnini R. Epidemiology and genetics of alopecia areata. Clin Exp Dermatol 2002;27:405-9.  Back to cited text no. 26
Biran R, Zlotogorski A, Ramot Y. The genetics of alopecia areata: New approaches, new findings, new treatments. J Dermatol Sci 2015;78:11-20.  Back to cited text no. 27
Betz RC, Petukhova L, Ripke S, Huang H, Menelaou A, Redler S, et al. Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. Nat Commun 2015;6:5966.  Back to cited text no. 28
Petukhova L, Christiano AM. Functional interpretation of genome-wide association study evidence in alopecia areata. J Invest Dermatol 2016;136:314-7.  Back to cited text no. 29
Petukhova L, Duvic M, Hordinsky M, Norris D, Price V, Shimomura Y, et al. Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. Nature 2010;466:113-7.  Back to cited text no. 30
Güleç AT, Tanriverdi N, Dürü C, Saray Y, Akçali C. The role of psychological factors in alopecia areata and the impact of the disease on the quality of life. Int J Dermatol 2004;43:352-6.  Back to cited text no. 31
Gupta MA, Gupta AK, Watteel GN. Stress and alopecia areata: A psychodermatologic study. Acta Derm Venereol 1997;77:296-8.  Back to cited text no. 32
Brajac I, Tkalcic M, Dragojević DM, Gruber F. Roles of stress, stress perception and trait-anxiety in the onset and course of alopecia areata. J Dermatol 2003;30:871-8.  Back to cited text no. 33
Zhang X, Yu M, Yu W, Weinberg J, Shapiro J, McElwee KJ, et al. Development of alopecia areata is associated with higher central and peripheral hypothalamic-pituitary-adrenal tone in the skin graft induced C3H/HeJ mouse model. J Invest Dermatol 2009;129:1527-38.  Back to cited text no. 34
Rodriguez TA, Duvic M; National Alopecia Areata Registry. Onset of alopecia areata after Epstein-Barr virus infectious mononucleosis. J Am Acad Dermatol 2008;59:137-9.  Back to cited text no. 35
Ito T, Tokura Y. The role of cytokines and chemokines in the T-cell-mediated autoimmune process in alopecia areata. Exp Dermatol 2014;23:787-91.  Back to cited text no. 36
McCusker M, Sidbury R. Nutrition and skin: Kids are not just little people. Clin Dermatol 2016;34:698-709.  Back to cited text no. 37
Paus R, Bertolini M. The role of hair follicle immune privilege collapse in alopecia areata: Status and perspectives. J Investig Dermatol Symp Proc 2013;16:S25-7.  Back to cited text no. 38
Paus R, Langan EA, Vidali S, Ramot Y, Andersen B. Neuroendocrinology of the hair follicle: Principles and clinical perspectives. Trends Mol Med 2014;20:559-70.  Back to cited text no. 39
Ito T, Aoshima M, Ito N, Uchiyama I, Sakamoto K, Kawamura T, et al. Combination therapy with oral PUVA and corticosteroid for recalcitrant alopecia areata. Arch Dermatol Res 2009;301:373-80.  Back to cited text no. 40
Olsen EA, Hordinsky MK, Price VH, Roberts JL, Shapiro J, Canfield D, et al. Alopecia areata investigational assessment guidelines – Part II. National alopecia areata foundation. J Am Acad Dermatol 2004;51:440-7.  Back to cited text no. 41
Pratt CH, King LE Jr., Messenger AG, Christiano AM, Sundberg JP. Alopecia areata. Nat Rev Dis Primers 2017;3:17011.  Back to cited text no. 42
Park KY, Jang WS, Son IP, Choi SY, Lee MY, Kim BJ, et al. Combination therapy with cyclosporine and psoralen plus ultraviolet a in the patients with severe alopecia areata: A retrospective study with a self-controlled design. Ann Dermatol 2013;25:12-6.  Back to cited text no. 43
Charuwichitratana S, Wattanakrai P, Tanrattanakorn S. Randomized double-blind placebo-controlled trial in the treatment of alopecia areata with 0.25% desoximetasone cream. Arch Dermatol 2000;136:1276-7.  Back to cited text no. 44
Kubeyinje EP. Intralesional triamcinolone acetonide in alopecia areata amongst 62 Saudi Arabs. East Afr Med J 1994;71:674-5.  Back to cited text no. 45
Jahn-Bassler K, Bauer WM, Karlhofer F, Vossen MG, Stingl G. Sequential high- and low-dose systemic corticosteroid therapy for severe childhood alopecia areata. J Dtsch Dermatol Ges 2017;15:42-7.  Back to cited text no. 46
Yoshimasu T, Kanazawa N, Yamamoto Y, Furukawa F. Multiple courses of pulse corticosteroid therapy for alopecia areata. J Dermatol 2016;43:1075-7.  Back to cited text no. 47
Kurosawa M, Nakagawa S, Mizuashi M, Sasaki Y, Kawamura M, Saito M, et al. Acomparison of the efficacy, relapse rate and side effects among three modalities of systemic corticosteroid therapy for alopecia areata. Dermatology 2006;212:361-5.  Back to cited text no. 48
Happle R. Antigenic competition as a therapeutic concept for alopecia areata. Arch Dermatol Res 1980;267:109-14.  Back to cited text no. 49
El Taieb MA, Ibrahim H, Nada EA, Seif Al-Din M. Platelets rich plasma versus minoxidil 5% in treatment of alopecia areata: A trichoscopic evaluation. Dermatologic therapy. 2017;30(1). Epub 2016/10/30. doi: 10.1111/dth.12437. PubMed PMID: 27791311.  Back to cited text no. 50
Al-Mutairi N. 308-nm excimer laser for the treatment of alopecia areata. Dermatol Surg 2007;33:1483-7.  Back to cited text no. 51
Castela E, Le Duff F, Butori C, Ticchioni M, Hofman P, Bahadoran P, et al. Effects of low-dose recombinant interleukin 2 to promote T-regulatory cells in alopecia areata. JAMA Dermatol 2014;150:748-51.  Back to cited text no. 52
Hordinsky M, Kaplan DH. Low-dose interleukin 2 to reverse alopecia areata. JAMA Dermatol 2014;150:696-7.  Back to cited text no. 53
Zorn E, Nelson EA, Mohseni M, Porcheray F, Kim H, Litsa D, et al. IL-2 regulates FOXP3 expression in human CD4+CD25+regulatory T cells through a STAT-dependent mechanism and induces the expansion of these cells in vivo. Blood 2006;108:1571-9.  Back to cited text no. 54
Tanemura A, Oiso N, Nakano M, Itoi S, Kawada A, Katayama I, et al. Alopecia areata: Infiltration of th17 cells in the dermis, particularly around hair follicles. Dermatology 2013;226:333-6.  Back to cited text no. 55
Lew BL, Cho HR, Haw S, Kim HJ, Chung JH, Sim WY, et al. Association between IL17A/IL17RA gene polymorphisms and susceptibility to alopecia areata in the Korean population. Ann Dermatol 2012;24:61-5.  Back to cited text no. 56
Elela MA, Gawdat HI, Hegazy RA, Fawzy MM, Abdel Hay RM, Saadi D, et al. Bcell activating factor and T-helper 17 cells: Possible synergistic culprits in the pathogenesis of alopecia areata. Arch Dermatol Res 2016;308:115-21.  Back to cited text no. 57
Chikhalkar S, Jerajani H, Madke B. Evaluation of utility of phenol in alopecia areata. Int J Trichology 2013;5:179-84.  Back to cited text no. 58
Savant SS, Shenoy S. Chemical peeling with phenol: For the treatment of stable vitiligo and alopecia areata. Indian J Dermatol Venereol Leprol 1999;65:93-8.  Back to cited text no. 59
  [Full text]  
Wikramanayake TC, Villasante AC, Mauro LM, Perez CI, Schachner LA, Jimenez JJ, et al. Prevention and treatment of alopecia areata with quercetin in the C3H/HeJ mouse model. Cell Stress Chaperones 2012;17:267-74.  Back to cited text no. 60
Kim HM, Lim YY, Kim MY, Son IP, Kim DH, Park SR, et al. Inhibitory effect of tianeptine on catagen induction in alopecia areata-like lesions induced by ultrasonic wave stress in mice. Clin Exp Dermatol 2013;38:758-67.  Back to cited text no. 61
Perini G, Zara M, Cipriani R, Carraro C, Preti A, Gava F, et al. Imipramine in alopecia areata. A double-blind, placebo-controlled study. Psychother Psychosom 1994;61:195-8.  Back to cited text no. 62
Cipriani R, Perini GI, Rampinelli S. Paroxetine in alopecia areata. Int J Dermatol 2001;40:600-1.  Back to cited text no. 63
Katikaneni R, Seymour AW, Gulati R, Ponnapakkam T, Gensure RC. Therapy for alopecia areata in mice by stimulating the hair cycle with parathyroid hormone agonists linked to a collagen-binding domain. J Investig Dermatol Symp Proc 2015;17:13-5.  Back to cited text no. 64
Wikramanayake TC, Rodriguez R, Choudhary S, Mauro LM, Nouri K, Schachner LA, et al. Effects of the lexington LaserComb on hair regrowth in the C3H/HeJ mouse model of alopecia areata. Lasers Med Sci 2012;27:431-6.  Back to cited text no. 65
King LE Jr., Silva KA, Kennedy VE, Sundberg JP. Lack of response to laser comb in spontaneous and graft-induced alopecia areata in C3H/HeJ mice. J Invest Dermatol 2014;134:264-6.  Back to cited text no. 66
Waiz M, Saleh AZ, Hayani R, Jubory SO. Use of the pulsed infrared diode laser (904 nm) in the treatment of alopecia areata. J Cosmet Laser Ther 2006;8:27-30.  Back to cited text no. 67
Sundberg JP, McElwee KJ, Carroll JM, King LE Jr. Hypothesis testing: CTLA4 co-stimulatory pathways critical in the pathogenesis of human and mouse alopecia areata. J Invest Dermatol 2011;131:2323-4.  Back to cited text no. 68
Sundberg JP, Cordy WR, King LE Jr. Alopecia areata in aging C3H/HeJ mice. J Invest Dermatol 1994;102:847-56.  Back to cited text no. 69
John KK, Brockschmidt FF, Redler S, Herold C, Hanneken S, Eigelshoven S, et al. Genetic variants in CTLA4 are strongly associated with alopecia areata. J Invest Dermatol 2011;131:1169-72.  Back to cited text no. 70
Keating GM. Abatacept: A review of its use in the management of rheumatoid arthritis. Drugs 2013;73:1095-119.  Back to cited text no. 71
Xing L, Dai Z, Jabbari A, Cerise JE, Higgins CA, Gong W, et al. Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition. Nat Med 2014;20:1043-9.  Back to cited text no. 72
Anzengruber F, Maul JT, Kamarachev J, Trüeb RM, French LE, Navarini AA, et al. Transient efficacy of tofacitinib in alopecia areata universalis. Case Rep Dermatol 2016;8:102-6.  Back to cited text no. 73
Mackay-Wiggan J, Jabbari A, Nguyen N, Cerise JE, Clark C, Ulerio G, et al. Oral ruxolitinib induces hair regrowth in patients with moderate-to-severe alopecia areata. JCI Insight 2016;1:e89790.  Back to cited text no. 74
Kennedy Crispin M, Ko JM, Craiglow BG, Li S, Shankar G, Urban JR, et al. Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata. JCI Insight 2016;1:e89776.  Back to cited text no. 75
Li ZJ, Choi HI, Choi DK, Sohn KC, Im M, Seo YJ, et al. Autologous platelet-rich plasma: A potential therapeutic tool for promoting hair growth. Dermatol Surg 2012;38:1040-6.  Back to cited text no. 76
Trink A, Sorbellini E, Bezzola P, Rodella L, Rezzani R, Ramot Y, et al. Arandomized, double-blind, placebo- and active-controlled, half-head study to evaluate the effects of platelet-rich plasma on alopecia areata. Br J Dermatol 2013;169:690-4.  Back to cited text no. 77
d'Ovidio R, Roberto M. Limited effectiveness of platelet-rich-plasma treatment on chronic severe alopecia areata. Hair Ther Transplant 2014;4. DOI: 10.4172/2167-0951.1000116.  Back to cited text no. 78
Lattouf C, Jimenez JJ, Tosti A, Miteva M, Wikramanayake TC, Kittles C, et al. Treatment of alopecia areata with simvastatin/ezetimibe. J Am Acad Dermatol 2015;72:359-61.  Back to cited text no. 79
Tajiri K, Shimojo N, Sakai S, Machino-Ohtsuka T, Imanaka-Yoshida K, Hiroe M, et al. Pitavastatin regulates helper T-cell differentiation and ameliorates autoimmune myocarditis in mice. Cardiovasc Drugs Ther 2013;27:413-24.  Back to cited text no. 80
Egesi A, Sun G, Khachemoune A, Rashid RM. Statins in skin: Research and rediscovery, from psoriasis to sclerosis. J Drugs Dermatol 2010;9:921-7.  Back to cited text no. 81
Loi C, Starace M, Piraccini BM. Alopecia areata (AA) and treatment with simvastatin/ezetimibe: Experience of 20 patients. J Am Acad Dermatol 2016;74:e99-e100.  Back to cited text no. 82
Thompson JM, Mirza MA, Park MK, Qureshi AA, Cho E. The role of micronutrients in alopecia areata: A review. Am J Clin Dermatol 2017;18:663-79.  Back to cited text no. 83
Holler PD, Cotsarelis G. Retinoids putting the “a” in alopecia. J Invest Dermatol 2013;133:285-6.  Back to cited text no. 84
Duncan FJ, Silva KA, Johnson CJ, King BL, Szatkiewicz JP, Kamdar SP, et al. Endogenous retinoids in the pathogenesis of alopecia areata. J Invest Dermatol 2013;133:334-43.  Back to cited text no. 85
Suo L, Sundberg JP, Everts HB. Dietary vitamin A regulates wingless-related MMTV integration site signaling to alter the hair cycle. Exp Biol Med (Maywood) 2015;240:618-23.  Back to cited text no. 86
Gould TD, Chen G, Manji HK.In vivo evidence in the brain for lithium inhibition of glycogen synthase kinase-3. Neuropsychopharmacology 2004;29:32-8.  Back to cited text no. 87
Rosenberg G. The mechanisms of action of valproate in neuropsychiatric disorders: Can we see the forest for the trees? Cell Mol Life Sci 2007;64:2090-103.  Back to cited text no. 88
Lee SH, Yoon J, Shin SH, Zahoor M, Kim HJ, Park PJ, et al. Valproic acid induces hair regeneration in murine model and activates alkaline phosphatase activity in human dermal papilla cells. PLoS One 2012;7:e34152.  Back to cited text no. 89
Singh A, Yadav S. Microneedling: Advances and widening horizons. Indian Dermatol Online J 2016;7:244-54.  Back to cited text no. 90
[PUBMED]  [Full text]  
Dhurat R, Sukesh M, Avhad G, Dandale A, Pal A, Pund P, et al. Arandomized evaluator blinded study of effect of microneedling in androgenetic alopecia: A pilot study. Int J Trichology 2013;5:6-11.  Back to cited text no. 91
Chandrashekar B, Yepuri V, Mysore V. Alopecia areata-successful outcome with microneedling and triamcinolone acetonide. J Cutan Aesthet Surg 2014;7:63-4.  Back to cited text no. 92
[PUBMED]  [Full text]  
Ito T, Yoshimasu T, Furukawa F, Nakamura M, Tokura Y. Three-microneedle device as an effective option for intralesional corticosteroid administration for the treatment of alopecia areata. J Dermatol 2017;44:e304-5.  Back to cited text no. 93
Deepak SH, Shwetha S. Scalp roller therapy in resistant alopecia areata. J Cutan Aesthet Surg 2014;7:61-2.  Back to cited text no. 94
[PUBMED]  [Full text]  


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[Pubmed] | [DOI]
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G. Kyriakou, V. Drivelou, A. Glentis
British Journal of Dermatology. 2021; 184(1): 156
[Pubmed] | [DOI]
49 The epidemiology of alopecia areata: a population-based cohort study in UK primary care
M. Harries, A.E. Macbeth, S. Holmes, W.S. Chiu, W.R. Gallardo, M. Nijher, S. Lusignan, C. Tziotzios, A.G. Messenger
British Journal of Dermatology. 2021;
[Pubmed] | [DOI]
50 Troponin I in alopecia areata and female pattern hair loss
MohammedA Shoeib, OlaA Bakry, ShimaaE Soliman, AmiraS Iraqi
Menoufia Medical Journal. 2021; 34(2): 498
[Pubmed] | [DOI]
51 A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
Kerry-Ann L Dillon
Clinical, Cosmetic and Investigational Dermatology. 2021; Volume 14: 691
[Pubmed] | [DOI]
52 Treatment of alopecia totalis/universalis/focalis with vitamin D and analogs: Three case reports and a literature review
Dimitrios T Papadimitriou, Christina Bothou, Eleni Dermitzaki, Alexios Alexopoulos, George Mastorakos
World Journal of Clinical Pediatrics. 2021; 10(6): 192
[Pubmed] | [DOI]
53 Association Between Vitamin D and Zinc Levels With Alopecia Areata Phenotypes at a Tertiary Care Center
Saeed M Alamoudi, Siham M Marghalani, Rakan S Alajmi, Yara E Aljefri , Abdullah F Alafif
Cureus. 2021;
[Pubmed] | [DOI]
54 Illness perception in patients with Alopecia areata under topical immunotherapy
Maryam Nasimi, Robabeh Abedini, Narges Ghandi, Fatememasume Manuchehr, Amirmasoud Kazemzadeh Houjaghan, Safoura Shakoei
Dermatologic Therapy. 2021; 34(2)
[Pubmed] | [DOI]
55 Chemical Gastroenterocolitis after Dental Root Canal Therapy with Camphorated and Mentholated Chlorophenol
Mikheil Kalandarishvili, Ernst-Wolfgang Kolbe, Günther Winde, Michael Kaspari, Chia-Tung Shun
Case Reports in Gastrointestinal Medicine. 2021; 2021: 1
[Pubmed] | [DOI]
56 ?linical case of focal alopecia in a child with atopy
A. A. Barilo, S. V. Smirnova, I. M. Olyanina
Medical Immunology (Russia). 2021; 23(1): 191
[Pubmed] | [DOI]
57 Design of In Vitro Hair Follicles for Different Applications in the Treatment of Alopecia—A Review
Matej Žnidaric, Žan Michel Žurga, Uroš Maver
Biomedicines. 2021; 9(4): 435
[Pubmed] | [DOI]

A Retrospective Comparative Study of Two Concentrations of Intralesional Triamcinolone Acetonide in the Treatment of Patchy Alopecia Areata on the Scalp

Jihan M Muhaidat, Firas Al-Qarqaz, Yousef Khader, Diala M Alshiyab, Hadeel Alkofahi, Mohanad Almalekh
Clinical, Cosmetic and Investigational Dermatology. 2020; Volume 13: 795
[Pubmed] | [DOI]
Inessa Mykhailivna Serbina
International Medical Journal. 2020; (3): 73
[Pubmed] | [DOI]
60 Alopecia - overview, causes and current treatment options
Emanuel Marques, Milena Tanczosová, Monika Arenbergerová
Dermatologie pro praxi. 2020; 14(3): 124
[Pubmed] | [DOI]
61 Successful Treatment of Alopecia Areata Patches with Triamcinolone Acetonide Using MMP®: Report of 2 Cases
Marina Barletta, Luciana Gasques
Skin Appendage Disorders. 2020; 6(4): 229
[Pubmed] | [DOI]
62 Prevalence and Clinical Characteristics of Alopecia Areata at a Tertiary Care Center in Saudi Arabia
Aysha A. Alshahrani, Rawan Al-Tuwaijri, Zainah A. Abuoliat, Mesnad Alyabsi, Mohammed I. AlJasser, Rayan Alkhodair
Dermatology Research and Practice. 2020; 2020: 1
[Pubmed] | [DOI]
63 Systemic Lupus Erythematosus Presenting as Alopecia Areata
Parnia Forouzan, Philip R Cohen
Cureus. 2020;
[Pubmed] | [DOI]
64 Bidirectional association between alopecia areata and atopic dermatitis: A population-based cohort study in Taiwan
Yu-Hsun Wei, Ying-Hsuan Tai, Ying-Xiu Dai, Yun-Ting Chang, Tzeng-Ji Chen, Mu-Hong Chen
Clinical & Experimental Allergy. 2020; 50(12): 1406
[Pubmed] | [DOI]
65 Analysis of dermatologic conditions in Turkey and Italy by using Google Trends analysis in the era of the COVID -19 pandemic
Ömer Kutlu
Dermatologic Therapy. 2020; 33(6)
[Pubmed] | [DOI]
66 Platelet-Rich Plasma in the Treatment of Alopecia Areata: A Review
Hind M. Almohanna, Azhar A. Ahmed, Jacob W. Griggs, Antonella Tosti
Journal of Investigative Dermatology Symposium Proceedings. 2020; 20(1): S45
[Pubmed] | [DOI]
67 Efficacy of Postbiotics in a PRP-Like Cosmetic Product for the Treatment of Alopecia Area Celsi: A Randomized Double-Blinded Parallel-Group Study
Fabio Rinaldi, Anna Trink, Daniela Pinto
Dermatology and Therapy. 2020; 10(3): 483
[Pubmed] | [DOI]
68 Aktuelles zur Alopecia areata
Ulrich Mutschler
Pädiatrie. 2018; 30(4): 14
[Pubmed] | [DOI]


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