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Research 241–270 of 1000+
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- First Symposium of Ichthyosis Experts
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- A generalized reticulate eruption with scarring alopecia, vulvovaginitis, keratoderma, and 20-nail dystrophy in a 70-year-old woman
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Late presentation of myotonic dystrophy
- Hypotrichosis with juvenile macular dystrophy
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Practice and Educational Gaps in Dermatology
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- FOXN1 deficient nude severe combined immunodeficiency
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair