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Research 331–360 of 1000+
- Successful Treatment of Temporal Triangular Alopecia with Topical Minoxidil
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- PSEUDOPELADE: AN INHERITED ALOPECIA
- An intrafamilial transmission of<i>Arthroderma benhamiae</i>in Canadian porcupines (<i>Erethizon dorsatum</i>) in a Japanese zoo
- Pregnancy's effects on the skin
- Phrynoderma and acquired acrodermatitis enteropathica in breastfeeding women after bariatric surgery
- Platelet-Rich Plasma (PRP) for Endometrial Treatment Efficacy and Safety in Assisted Reproductive Technology: A Comprehensive Review
- Pregnancy during the course of Cushing’s syndrome: a case report and literature review
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Monilethrix in three generations
- 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
- Precocious Pubarche in a 7-Year-Old Patient. A Case Report
- 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