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Absence of molecular defect in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3 beta-HSD activity.
Chang YT, Zhang L, Alkaddour HS, Mason JI, Lin K, Yang X, Garibaldi LR, Bourdony CJ, Dolan LM, Donaldson DL, et al. Chang YT, et al. Among authors: donaldson dl. Pediatr Res. 1995 Jun;37(6):820-4. doi: 10.1203/00006450-199506000-00024. Pediatr Res. 1995. PMID: 7651769
Clinical complexity and impact of the ABC (Atrial fibrillation Better Care) pathway in patients with atrial fibrillation: a report from the ESC-EHRA EURObservational Research Programme in AF General Long-Term Registry.
Romiti GF, Proietti M, Vitolo M, Bonini N, Fawzy AM, Ding WY, Fauchier L, Marin F, Nabauer M, Dan GA, Potpara TS, Boriani G, Lip GYH; ESC-EHRA EORP-AF General Long-Term Registry Investigators. Romiti GF, et al. BMC Med. 2022 Sep 2;20(1):326. doi: 10.1186/s12916-022-02526-7. BMC Med. 2022. PMID: 36056426 Free PMC article.
Epidemiology and impact of frailty in patients with atrial fibrillation in Europe.
Proietti M, Romiti GF, Vitolo M, Harrison SL, Lane DA, Fauchier L, Marin F, Näbauer M, Potpara TS, Dan GA, Maggioni AP, Cesari M, Boriani G, Lip GYH; ESC-EHRA EORP-AF General Long-Term Registry Investigators. Proietti M, et al. Age Ageing. 2022 Aug 2;51(8):afac192. doi: 10.1093/ageing/afac192. Age Ageing. 2022. PMID: 35997262
750 results