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Research 751–780 of 1000+
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Office Diagnosis of Hair Shaft Defects
- FOXN1 deficient nude severe combined immunodeficiency
- Premature Adrenarche
- Cardiovascular risk factors and events in women with androgen excess
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Hairless is a nuclear receptor corepressor essential for skin function
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Management of CAH during pregnancy
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Hormone therapy in acne
- Hirsutism in the United Arab Emirates: a hospital study
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Alopecia: A Pathologist's View
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Endocrinology of Hirsutism: From Androgens to Androgen Excess Disorders
- Secondary cicatricial and other permanent alopecias
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Evaluation and Treatment of Hirsutism in Premenopausal Women
- Polycystic ovary syndrome and the differential diagnosis of hyperandrogenism
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Difficult and rare forms of acne
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Hair follicles and their role in skin health
- Ptosis in childhood
- Approach to androgen excess in women: Clinical and biochemical insights
- Helpful diagnostic markers of steroidogenesis for defining hyperandrogenemia in hirsute women
- Nonclassic 21-hydroxylase deficiency
- Natural hair patterns