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Research 451–480 of 1000+
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Differences between ultrastructure and protein composition in straight hair fibres
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Abnormal fingerprints and immigration delay disease
- The rising burden of alopecia: A review on aetiology, prevalence and role of homoeopathy
- Christmas article: Case of uncombable hair syndrome discovered after publication of article in Ugeskrift for Læger
- Unruly hair
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Hypotrichosis in a child with olmsted syndrome
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- Molecular mechanisms of ectodermal dysplasia syndromes
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Genetic characterization of congenital defects in dogs : caudal dysplasia, ectodermal dysplasia and mucopolysaccharidosis VII
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Salivary gland function in persons with ectodermal dysplasias
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Topical minoxidil treatment for congenital alopecia in hypohidrotic ectodermal dysplasia