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Research 61–90 of 1000+
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- Topical minoxidil treatment for congenital alopecia 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
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Clinical Snippets
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Lymphoproliferative Disorders: Hot Topics in Dermatology 2019
- Becker's nevus associated with chromosomal mosaicism and congenital adrenal hyperplasia
- Index
- Skin Development and Disease: A Molecular Perspective
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- The hair shaft: normality, abnormality, and genetics
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Trichoscopy in genetic hair shaft abnormalities
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Molecular Genetics of Alopecias
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- HAIR MATRIX CELL KINETICS: A SELECTIVE REVIEW