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Research 151–180 of 1000+
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Congenital Copper Deficiency: Copper Therapy and Dopamine‐β‐Hydroxylase Activity in the Mottled (Brindled) Mouse
- Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia
- Hair and scalp disorders
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- Ulerythema ophryogenes with multiple congenital anomalies
- Disorders of hair growth : diagnosis and treatment
- The Hirsute Woman: Challenges in Evaluation and Management
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Case Report: Disorder of Sex Development 46, XY with Proximal Hypospadias in a 10-Year-Old Twin Boy: Disorder of Sex Development 46, XY with Proximal Hypospadias
- Congenital and Hereditary Skin Diseases
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- What Work-Up Should Be Done for Patients With Alopecia?
- KRT16 wt Allele
- Disorders of the Hair and Nails
- Dermatoscopy of hair shaft disorders
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Disorders of Hair Pigmentation
- Non-classic congenital adrenal hyperplasia
- Hair physiology and its disorders
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)