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Research 91–120 of 1000+
- Hairless is a nuclear receptor corepressor essential for skin function
- Hairless: A nuclear receptor corepressor essential for skin function
- Alopecia: A Pathologist's View
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- RECENT DEVELOPMENTS IN ALOPECIAS
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Papular atrichia
- A clinician's approach to canine alopecia
- The eye and the skin in endocrine metabolic diseases
- Triangular Temporal Alopecia - Two Case Reports, Dermoscopy and Review
- Coat Problems
- Alopezien und Hypotrichosen im Kindesalter
- Le gène<i>hairless</i>de la souris
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Diagnostic Criteria for Polycystic Ovarian Syndrome
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Secondary cicatricial and other permanent alopecias
- Polycystic ovary syndrome and the differential diagnosis of hyperandrogenism
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Nonclassic 21-hydroxylase deficiency
- Androgen excess and post-reproductive health
- Alopecia in children
- Clinical and Investigative Study of Hirsutism
- Alopecia universalis and Kallman’s Syndrome
- Diseases of the Scalp
- 7696 Ovarian Steroid Cell Tumor Presenting As Non-classical Adrenal Hyperplasia
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS