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Research 811–840 of 1000+
- An Excellent Response to Tofacitinib in a Pediatric Alopecia Patient: A Case Report and Review.
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Don't miss this blue toe: Hair tourniquet syndrome
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Aplasia cutis congenita on lumbosacral area
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- Does a picture of the human placenta predict the future?
- Familial Frontal Fibrosing Alopecia
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Three cases of hair loss analyzed by the point of view of the analytical psychology
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- 61349 The Development of Vitiligo After Cessation of Finasteride: Is this Part of Post-Finasteride Syndrome or an Adverse Event of Finasteride?
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Hyperpigmentation in a child as a clue to chikungunya
- Pure Leydig cell tumor of the ovary: a rare presentation of a rare entity in a pregnant patient
- ABORTION AROUND THE WORLD- LOOKING FOR THE GOLDEN MEAN
- Pearly Pinna Papules in a Young Female
- An overview of risk factors for androgenetic alopecia among women at Pasar Ambacang, Kuranji, Padang
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- A rare case of pemphigus vulgaris in pregnancy
- Precocious puberty in a 24 month old Nigerian girl: case report
- SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION
- 017 Lichen Planus Colocalized with Vitiligo: Coincidence?
- Chemotherapy-Induced Alopecia and Quality-of-Life: Ovarian and Uterine Cancer Patients and the Aesthetics of Disease
- Diffuse hypotrichosis from early childhood
- G367(P) A chubby child: is this a sign of health or malnutrition?
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis