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10. Misspelled Author Name in the Byline. JAMA Pediatr; 2022 Jan; 176(1):104. PubMed ID: 34779828 [No Abstract] [Full Text] [Related]
11. Misspelled Author Name in the Byline. JAMA Pediatr; 2021 Apr; 175(4):435. PubMed ID: 33587097 [No Abstract] [Full Text] [Related]
12. Misspelled Author Name and Funding Source. JAMA Oncol; 2021 Feb; 7(2):312. PubMed ID: 33331848 [No Abstract] [Full Text] [Related]
13. Correction to: Stingray spear injury to the pediatric spinal cord: case report and review of the literature. Caceres A; Shlobin NA; Lam S; Zamora J; Segura JL Childs Nerv Syst; 2020 Aug; 36(8):1817. PubMed ID: 32583149 [TBL] [Abstract][Full Text] [Related]
14. Author Correction: Spatially resolved steady-state negative capacitance. Yadav AK; Nguyen KX; Hong Z; García-Fernández P; Aguado-Puente P; Nelson CT; Das S; Prasad B; Kwon D; Cheema S; Khan AI; Hu C; Íñiguez J; Junquera J; Chen LQ; Muller DA; Ramesh R; Salahuddin S Nature; 2019 Apr; 568(7753):E13. PubMed ID: 30971827 [TBL] [Abstract][Full Text] [Related]
15. Publisher Correction: Viewpoints: how the hippocampus contributes to memory, navigation and cognition. Lisman J; Buzsáki G; Eichenbaum H; Nadel L; Ranganath C; Redish AD Nat Neurosci; 2018 Jul; 21(7):1018. PubMed ID: 29263406 [TBL] [Abstract][Full Text] [Related]
16. Author Correction: Predicting the clinical impact of human mutation with deep neural networks. Sundaram L; Gao H; Padigepati SR; McRae JF; Li Y; Kosmicki JA; Fritzilas N; Hakenberg J; Dutta A; Shon J; Xu J; Batzoglou S; Li X; Farh KK Nat Genet; 2019 Feb; 51(2):364. PubMed ID: 30559491 [TBL] [Abstract][Full Text] [Related]
17. Correction to: Burden of caregivers of adult patients with schizophrenia in a predominantly African ancestry population. Alexander G; Bebee CE; Chen KM; Vignes RD; Dixon B; Escoffery R; Francis C; Francis D; Mendoza Z; Miller S; Montano S; Nelson M; Ramcharan S; Richards S; Jackson MD Qual Life Res; 2019 May; 28(5):1387. PubMed ID: 30635849 [TBL] [Abstract][Full Text] [Related]
18. Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia. Cortese A; Simone R; Sullivan R; Vandrovcova J; Tariq H; Yau WY; Humphrey J; Jaunmuktane Z; Sivakumar P; Polke J; Ilyas M; Tribollet E; Tomaselli PJ; Devigili G; Callegari I; Versino M; Salpietro V; Efthymiou S; Kaski D; Wood NW; Andrade NS; Buglo E; Rebelo A; Rossor AM; Bronstein A; Fratta P; Marques WJ; Züchner S; Reilly MM; Houlden H Nat Genet; 2019 May; 51(5):920. PubMed ID: 31028356 [TBL] [Abstract][Full Text] [Related]
19. Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research. Sirota M; Thomas CG; Liu R; Zuhl M; Banerjee P; Wong RJ; Quaintance CC; Leite R; Chubiz J; Anderson R; Chappell J; Kim M; Grobman W; Zhang G; Rokas A; Muglia LJ; Ober C; England SK; Macones G; Driscoll D; Parry S; Shaw GM; Stevenson DK; Simpson JL; Thomson E; Butte AJ; Sci Data; 2018 Dec; 5(1):3. PubMed ID: 30563979 [TBL] [Abstract][Full Text] [Related]
20. Correction to: Risk factors of premature rupture of membranes in public hospitals at Mekele city, Tigray, a case control study. Assefa NE; Berhe H; Girma F; Berhe K; Berhe YZ; Gebreheat G; Werid WM; Berhe A; Rufae HB; Welu G BMC Pregnancy Childbirth; 2018 Oct; 18(1):403. PubMed ID: 30326874 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]