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Research 61–90 of 1000+
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Congenital atrichia with papular lesions
- Familial Frontal Fibrosing Alopecia
- BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Alopecia fibrosante frontal em mulheres negras: aspectos clínicos, diagnósticos e terapêuticos
- Predictive Modeling of Hair Fall using Random Forest Algorithms
- Nonclassic adrenal hyperplasia
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Congenital adrenal hyperplasia
- FC056 The ideal catagen of the hair
- Clinical Snippets
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- New familial association between ocular coloboma and loose anagen syndrome
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Frontal fibrosing alopecia: a disease fascinating for the researcher, disappointing for the clinician and distressing for the patient