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Research 31–60 of 1000+
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Morpho-Regulation of Ectodermal Organs
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Alopecia in Cronkhite-Canada syndrome
- Ectodermal Dysplasia: Variable Expressions
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Trichoscopy in Hair Shaft Disorders
- <i>WNT10A</i> , dermatology and dentistry
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genetics of Structural Hair Disorders