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Research 181–210 of 1000+
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- Hair-Thread Tourniquet Syndrome: A Case Report and Literature Review
- Trichotillomania in children and adolescents: Review of the literature and case report
- Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Crystalline Cataract and Uncombable Hair
- Gender Differences in Response to COVID-19 Infection and Vaccination
- Physiologic changes and dermatoses of pregnancy
- Contraceptive implant use among inner city teens
- Hair-tourniquet syndrome ??? multiple toes and bilaterality
- Successful Treatment of Temporal Triangular Alopecia with Topical Minoxidil
- Symptomatic zinc deficiency in a full-term breast-fed infant
- <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
- Update on the therapeutic role of metformin in the management of polycystic ovary syndrome: Effects on pathophysiologic process and fertility outcomes
- 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
- Effects of the prenatal and postnatal nurturing environment on the phenotype and gut microbiota of mice with polycystic ovary syndrome induced by prenatal androgen exposure: a cross-fostering study
- Anorexia nervosa and reproduction: connecting brain to gonads
- Aplasia cutis congenita on lumbosacral area