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Research 841–870 of 1000+
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Alopecia X em cães: revisão
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Monilethrix: Beaded hair and hypotrichosis in a child
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Rates of polycystic ovary syndrome (PCOS) symptoms in relatives of patients with PCOS
- Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans
- Monilethrix
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Hypothyroidism in Dogs
- [Netherton's syndrome in two sisters].
- This Week in JAMA
- P‐41 Psychogenic alopecia by fur‐plucking in a family of seal‐point Siamese cats: three cases
- ABC of Dermatology: Diseases of the hair and scalp
- BIOCHEMICAL FACTORS INFLUENCING FAMILIAL HIRSUTISM IN THE SOUTHERN REGION OF KPK
- 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
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- Androgenetic alopecia updates: Pathophysiology, diagnosis and treatment
- Genetics Poly Cystic Ovary Syndrome
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players