Search
for
Sort by
Research 91–120 of 1000+
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases
- Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- A Comparative Study of a New Food Supplement, ViviScal®, with Fish Extract for the Treatment of Hereditary Androgenic Alopecia in Young Males
- Topical minoxidil therapy for hereditary male pattern alopecia.
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- 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 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 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