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Research 211–240 of 1000+
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Alopecia in Children
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Antihypertensive Agents in Dermatology
- E-Poster
- Hair & Cutaneous Development
- Author Index
- Subject Index
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Avian-Inspired Analogies in Dermatology
- Subject Index
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Mice Expressing a Mutant Krt75 (K6hf) Allele Develop Hair and Nail Defects Resembling Pachyonychia Congenita
- Hair and nail disorders
- British Hair and Nail Society
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Hair and nail disorders of childhood
- PA33 When bones speak through nails: insights from a paediatric case series
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Analysis of hair loss in young adults- A clinical study
- Keratins of the Human Hair Follicle