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Research 751–780 of 1000+
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- High‐Potency Topical Steroids: An Effective Therapy for Chronic Scalp Inflammation in Rapp–Hodgkin Ectodermal Dysplasia
- Pure Hair‐Nail Ectodermal Dysplasia: Expanding the HOXC13 Genotypic Spectrum
- Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with <i>AIRE</i> gene mutation (autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy, APECED syndrome) treated with ruxolitinib
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Parallels in signaling between development and regeneration in ectodermal organs
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome with Concomitant Lymphopenia: A Novel TP63 Mutation
- Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
- A Unique Case of Trichorrhexis Nodosa—"Bamboo Hairs"
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Trichoscopy in Hair Shaft Disorders
- Atrichia With Papular Lesions
- <i>WNT10A</i> , dermatology and dentistry
- Ectodysplasin research—Where to next?
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Ulerythema Ophryogenes
- Msx2 Supports Epidermal Competency during Wound-Induced Hair Follicle Neogenesis
- Genetics of Structural Hair Disorders
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Hair shaft disorders in children – An update