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Research 601–630 of 1000+
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Research Snippets
- Current advances in stem cell-based therapies for hair regeneration
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Current Genetics in Hair Diseases
- Androgenic alopecia and its association with metabolic syndrome
- Androgеnеtic Alopеcia Pathogеnеsis, Diagnosis, and Trеatmеnt
- Androgenetic alopecia updates: Pathophysiology, diagnosis and treatment
- Gene therapy for alopecia in type II rickets model rats using vitamin D receptor-expressing adenovirus vector
- Genetics Poly Cystic Ovary Syndrome
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Werner′s syndrome
- Ectodermal Dysplasia: Variable Expressions
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- A rare hair loss in children: Monilethrix
- Consecuencias civiles en el impago de la primera prima o sucesivas de la póliza de seguro en los juicios penales por accidente de tráfico: ¿tiene cobertura por la aseguradora el conductor?
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Epidermolysis bullosa in animals: a review
- Cases Report the Cronkhite-Canada Syndrome
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Cronkhite-Canada syndrome: An elusive gastrointestinal disorder with multisystem involvement-pathogenesis, diagnosis, and therapeutic strategies
- Clinical cases of Darier-White follicular dyskeratosis
- LibGuides: L3Y2 Tutorial 2022 - critical thinking: Claim 5: Caffeine reduces hair loss
- A Rare Case of Cronkhite-Canada Syndrome
- Androgenetic Alopecia
- Alopecia in children
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Monilethrix