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Research 361–390 of 1000+
- Research Snippets
- Congenital Hypotrichosis with Hair and Dental Ectodermal Features Responsive to Sublingual Minoxidil
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia
- Molecular mechanisms of ectodermal dysplasia syndromes
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Masquerading of trichotillomania in a family with monilethrix
- Dermoscopy Update: Review of its Extradiagnostic and Expanding Indications and Future Prospects
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- Lymphoproliferative Disorders: Hot Topics in Dermatology 2019
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- The Naked (N) Mutation, Chromosome 15
- Displasia folicular en un Doberman adulto de capa negra : un caso clínico
- Pathology in Practice
- Hair dysplasias
- Itchy Black Hair Bristles on Back
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Clinical Snippets
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Alopecia Areata with Renal Dysgenesis