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Research 451–480 of 1000+
- 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
- Update on Frontal Fibrosing Alopecia
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Nonclassic Congenital Adrenal Hyperplasia
- Premature graying of hair
- 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
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Congenital adrenal hyperplasia
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Curcumin derivatives inhibit testicular 17β-hydroxysteroid dehydrogenase 3
- 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
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Evaluation of Hair Loss
- May AMH levels distinguish LOCAH from PCOS among hirsute women?