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Research 391–420 of 1000+
- Nonclassic Congenital Adrenal Hyperplasia
- Premature graying of hair
- Differential Diagnosis of Hyperandrogenism in Women with Polycystic Ovary Syndrome
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Alopecia and Its homoeopathic treatment
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Hair shaft disorders
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Androgens and androgen receptor action in skin and hair follicles
- Polycystic ovary syndrome and impact on health
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- Monilethrix Treated with Minoxidil
- Review of oral minoxidil as treatment of hair disorders: in search of the perfect dose
- Association of type 2 diabetes with central-scalp hair loss in a large cohort study of African American women
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis