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Research 331–360 of 1000+
- 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
- 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
- An Approach to Hair Loss in Pediatric Primary Care
- 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