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Research 391–420 of 1000+
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation
- 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Hair growth promoting effects of adipose tissue-derived stem cells
- Premature graying of hair
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- 5-Alpha reductase deficiency
- <i>WNT10A</i> , dermatology and dentistry
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Congenital adrenal hyperplasia
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Focal and Generalized Alopecia
- Disease causing homozygous variants in the human hairless gene
- Hairless controls hair fate decision via Wnt/β–catenin signaling