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Research 481–510 of 1000+
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function <i>VDR</i> mutation
- Hereditary vitamin D rickets: a case series in a family
- Erythrocyte deformability and hereditary elliptocytosis
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Hereditary Chorea Associated With and Aggravated by Systemic Lupus Erythematosus
- Zebrafish Model of Hereditary Pigmentary Disorders
- [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis].
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- Iron Screening in Alopecia Areata Patients May Catch Hereditary Hemochromatosis Early
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- [Monilethrix is a hereditary hair shaft disorder].
- Hereditary, Congenital, and Acquired Alopecias
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Hereditary Androgenetic Alopecia and Minoxidil
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Topical Minoxidil Therapy in Hereditary Androgenetic Alopecia
- Monilethrix: A rare hereditary condition
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Treatments of hereditary hair loss (alopecia)
- Quantitative image analysis for hereditary hair disorders
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Case Study: Hereditary Cancer Genetic Testing in Unaffected Patients May Allow for Early Intervention and Aggressive Management
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria