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Research 931–960 of 1000+
- 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
- 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
- Potential application of PBM use in hair follicle organoid culture for the treatment of androgenic alopecia
- Clinical cases of Darier-White follicular dyskeratosis
- LibGuides: L3Y2 Tutorial 2022 - critical thinking: Claim 5: Caffeine reduces hair loss
- Androgenetic Alopecia
- Alopecia in children
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Value of dermoscopy for the diagnosis of monilethrix
- Beta thalassemia revealing hypothyroidism: A case report
- Beta thalassemia revealing hypothyroidism: A case report
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- Androgenetic Alopecia
- FINASTERIDE AS A TREATMENT FOR MALE ANDROGENETIC ALOPECIA
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Hair Shaft Dysplasias
- Self-Amplifying RNA Approach for Protein Replacement Therapy
- Hair and nail disorders of childhood