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Research 31–60 of 1000+
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- 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 Hypotrichosis and Localized Morphea: A New Clinical Entity
- 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].
- Hereditary, Congenital, and Acquired Alopecias
- Delphi Consensus on Attenuated Androgen Use for Long‐Term Prophylaxis in Hereditary Angioedema: AURA Project
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Isotretinoin-induced hair growth in a case of hereditary hypotrichosis simplex of the scalp: A promising therapeutic approach
- Molecular Basis of Hereditary Hair Diseases
- 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
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- [Monilethrix is a hereditary hair shaft disorder].
- Hereditary, Congenital, and Acquired Alopecias
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature