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Research 841–870 of 1000+
- 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
- Dermatopathology and molecular genetics
- AN UPDATE OF HAIR SHAFT DISORDERS
- Dermatologic manifestations of endocrine disorders
- 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
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Hirsutism causes and treatments.
- Side effects after artificial hair implants: 2 case reports
- The diagnosis of androgenetic alopecia in children: Considerations of pathophysiological plausibility
- LC-MS/MS improves screening towards 21-hydroxylase deficiency
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Alopecia in children
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- RECENT DEVELOPMENTS IN ALOPECIAS
- Methods of hair loss evaluation in patients with endocrine disorders.
- Testicular Steroidogenesis
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- An X-traordinary stroke
- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- Hair loss.