Search
for
Sort by
Research 481–510 of 1000+
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Alopecia: A Pathologist's View
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Endocrinology of Hirsutism: From Androgens to Androgen Excess Disorders
- 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
- Clinical relevance of hair microscopy in alopecia
- 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
- Dermatopathology and molecular genetics
- AN UPDATE OF HAIR SHAFT DISORDERS
- Scalp Repair Using Tissue Expanders
- Dermatologic manifestations of endocrine disorders
- Leptomeningeal angiomatosis accompanied by hair follicle nevus
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Androgen excess and post-reproductive health
- The eye and the skin in endocrine metabolic diseases
- Neonatal follicular mucinosis
- Finasteride in the Treatment of Hirsutism
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome