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Research 31–60 of 1000+
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Dysfunction of keratinocyte adhesion
- Hair shaft structures in EDAR induced ectodermal dysplasia
- 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
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Biology and Genetics of Hair
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Genetics of Structural Hair Disorders
- Inherited Disorders of the Hair
- Hair loss among a group of Egyptian children
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Congenital atrichia and hypotrichosis
- Genetic Hair Disorders: A Review
- Hair Loss in Children, Etiologies, and Treatment
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages 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
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- <i>WNT10A</i> , dermatology and dentistry
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Hair Shaft Dysplasias