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Research 691–720 of 1000+
- The Case Files
- Mesotherapy and PRP Treatment in Combination with Hair Loss in WomenCase Report
- Serum biotin levels in women complaining of hair loss
- Pancreatic cancer
- Case report on premature hair graying treated with Melitane 5% and oral hair supplements
- The Impact of Androgenic Alopecia on the Quality of Life of Male Individuals: A Cross-Sectional Study
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Topical minoxidil therapy in hereditary androgenetic alopecia
- 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
- 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
- Erythrocyte deformability and hereditary elliptocytosis
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- 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