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Research 601–630 of 1000+
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Pachyonychia congenita: Sporadic onset with mutation analysis
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Hair Disorders
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- 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
- Hair and nail disorders of childhood
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita
- Hair loss in infancy and childhood
- Severe Hirsutism in Non Classic Congenital Adrenal Hyperplasia: A Case Report and Literature Review
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII
- Iatrogenic Cushing's Syndrome in a Patient With Salt-Wasting Congenital Adrenal Hyperplasia (SWCAH)
- Alopecia triangularis congenita in combination with androgenetic alopecia
- Committee on database of hair restoration results on patients with cicatricial alopecia and hair diseases other than androgenetic alopecia
- A 7‐Year‐Old Male With a Linear Band‐Like Hair Patch
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- The Use of Micrografts and Minigrafts in the Aesthetic Reconstruction of the Face and Scalp
- Hairless is a nuclear receptor corepressor essential for skin function
- The Efficacy of Topical Minoxidil for Non-Scarring Alopecia: A Systematic Review
- A rare clinical image of hypertrichosis (Werewolf syndrome)
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Hairless: A nuclear receptor corepressor essential for skin function
- Hirsutism: Diagnosis and management
- Alternative uses of dermoscopy in daily clinical practice: An update
- Alopecia: A Pathologist's View
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions