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Research 31–60 of 1000+
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review
- Congenital Atrichia: A Case Report
- Hair loss in infancy and childhood
- Hair physiology and its disorders
- Disorders of hair in children
- Hair Loss in Children
- Hair loss in children.
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Disorders of hair growth : diagnosis and treatment
- Hair loss in infancy and childhood
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Disorders of the Hair and Nails
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Epidermal dysplasia and <i>Malassezia</i> infection in two West Highland White Terrier siblings: an inherited skin disorder or reaction to severe <i>Malassezia</i> infection?
- The Efficacy of Topical Minoxidil for Non-Scarring Alopecia: A Systematic Review
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Nonclassic 21-hydroxylase deficiency
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Differential diagnosis of alopetia in children and adolescents
- Hair follicles and their role in skin health
- Congenital Adrenal Hyperplasia
- Congenital triangular alopecia: A close mimicker of alopecia areata
- Clinical report of a Holstein's calf with ichthyosis.
- What Work-Up Should Be Done for Patients With Alopecia?
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases