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Research 181–210 of 1000+
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Hair Shaft Disorders
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- A Case of the Cons: How Contraception Confused Congenital Adrenal Hyperplasia for Conn
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Congenital Combined Melanocytic Nevus of the Scalp With Associated Alopecia Areata
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Temporal triangular alopecia and a review of 52 past cases
- Ectrodactyly, Soft‐Tissue Syndactyly, and Nodulocystic Acne: Coincidence or Association?
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Familial congenital generalized hypertrichosis
- Congenital atrichia with papular lesions
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- Sjogren-Larsson syndrome
- Short anagen syndrome: Case series and literature review
- NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: A new disease association
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Pallister-Killian Syndrome
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Becker's Nevus Syndrome
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Bilateral circumscribed haemangioma of the choroid not associated with systemic vascular syndrome