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Page 1
Sublimation in bright spots on (1) Ceres.
Nathues A, Hoffmann M, Schaefer M, Le Corre L, Reddy V, Platz T, Cloutis EA, Christensen U, Kneissl T, Li JY, Mengel K, Schmedemann N, Schaefer T, Russell CT, Applin DM, Buczkowski DL, Izawa MR, Keller HU, O'Brien DP, Pieters CM, Raymond CA, Ripken J, Schenk PM, Schmidt BE, Sierks H, Sykes MV, Thangjam GS, Vincent JB. Nathues A, et al. Among authors: mengel k. Nature. 2015 Dec 10;528(7581):237-40. doi: 10.1038/nature15754. Nature. 2015. PMID: 26659183
Brine residues and organics in the Urvara basin on Ceres.
Nathues A, Hoffmann M, Schmedemann N, Sarkar R, Thangjam G, Mengel K, Hernandez J, Hiesinger H, Pasckert JH. Nathues A, et al. Among authors: mengel k. Nat Commun. 2022 Feb 22;13(1):927. doi: 10.1038/s41467-022-28570-8. Nat Commun. 2022. PMID: 35194036 Free PMC article.
Long-term Safety and Efficacy of Avalglucosidase Alfa in Patients With Late-Onset Pompe Disease.
Dimachkie MM, Barohn RJ, Byrne B, Goker-Alpan O, Kishnani PS, Ladha S, Laforêt P, Mengel KE, Peña LDM, Sacconi S, Straub V, Trivedi J, Van Damme P, van der Ploeg AT, Vissing J, Young P, Haack KA, Foster M, Gilbert JM, Miossec P, Vitse O, Zhou T, Schoser B; NEO-EXT investigators. Dimachkie MM, et al. Among authors: mengel ke. Neurology. 2022 Aug 1;99(5):e536-e548. doi: 10.1212/WNL.0000000000200746. Neurology. 2022. PMID: 35618441 Free PMC article.
Safety, tolerability, pharmacokinetics, pharmacodynamics, and exploratory efficacy of the novel enzyme replacement therapy avalglucosidase alfa (neoGAA) in treatment-naïve and alglucosidase alfa-treated patients with late-onset Pompe disease: A phase 1, open-label, multicenter, multinational, ascending dose study.
Pena LDM, Barohn RJ, Byrne BJ, Desnuelle C, Goker-Alpan O, Ladha S, Laforêt P, Mengel KE, Pestronk A, Pouget J, Schoser B, Straub V, Trivedi J, Van Damme P, Vissing J, Young P, Kacena K, Shafi R, Thurberg BL, Culm-Merdek K, van der Ploeg AT; NEO1 Investigator Group. Pena LDM, et al. Among authors: mengel ke. Neuromuscul Disord. 2019 Mar;29(3):167-186. doi: 10.1016/j.nmd.2018.12.004. Epub 2018 Dec 17. Neuromuscul Disord. 2019. PMID: 30770310 Free article. Clinical Trial.
Long-term outcomes of systemic therapies for Hurler syndrome: an international multicenter comparison.
Eisengart JB, Rudser KD, Xue Y, Orchard P, Miller W, Lund T, Van der Ploeg A, Mercer J, Jones S, Mengel KE, Gökce S, Guffon N, Giugliani R, de Souza CFM, Shapiro EG, Whitley CB. Eisengart JB, et al. Among authors: mengel ke. Genet Med. 2018 Nov;20(11):1423-1429. doi: 10.1038/gim.2018.29. Epub 2018 Mar 8. Genet Med. 2018. PMID: 29517765 Free PMC article.
Corrigendum to "Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases" [Mol. Genet. Metab. 118 (2016) 206-213].
Cassiman D, Packman S, Bembi B, Turkia HB, Al-Sayed M, Schiff M, Imrie J, Mabe P, Takahashi T, Mengel KE, Giugliani R, Cox GF. Cassiman D, et al. Among authors: mengel ke. Mol Genet Metab. 2018 Dec;125(4):360. doi: 10.1016/j.ymgme.2017.09.005. Epub 2017 Nov 10. Mol Genet Metab. 2018. PMID: 29129654 No abstract available.
49 results