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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1979 1
1980 2
1981 3
1982 4
1983 1
1984 1
1986 2
1987 2
1988 3
1989 3
1990 4
1991 1
1992 2
1993 2
1994 2
1995 4
1997 2
1999 1
2000 1
2001 2
2002 2
2003 2
2004 4
2005 6
2006 2
2007 3
2008 3
2009 2
2010 7
2011 7
2012 4
2013 4
2014 3
2015 2
2016 3
2017 3
2018 1
2019 2
2020 2
2025 1

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98 results

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Page 1
Dystonia and parkinsonism in GM1 type 3 gangliosidosis.
Roze E, Paschke E, Lopez N, Eck T, Yoshida K, Maurel-Ollivier A, Doummar D, Caillaud C, Galanaud D, Billette de Villemeur T, Vidailhet M, Roubergue A. Roze E, et al. Among authors: paschke e. Mov Disord. 2005 Oct;20(10):1366-9. doi: 10.1002/mds.20593. Mov Disord. 2005. PMID: 15986423 Review.
The Clinical and Molecular Spectrum of GM1 Gangliosidosis.
Arash-Kaps L, Komlosi K, Seegräber M, Diederich S, Paschke E, Amraoui Y, Beblo S, Dieckmann A, Smitka M, Hennermann JB. Arash-Kaps L, et al. Among authors: paschke e. J Pediatr. 2019 Dec;215:152-157.e3. doi: 10.1016/j.jpeds.2019.08.016. J Pediatr. 2019. PMID: 31761138
A new type of pharmacological chaperone for GM1-gangliosidosis related human lysosomal β-galactosidase: N-Substituted 5-amino-1-hydroxymethyl-cyclopentanetriols.
Schalli M, Weber P, Tysoe C, Pabst BM, Thonhofer M, Paschke E, Stütz AE, Tschernutter M, Windischhofer W, Withers SG. Schalli M, et al. Among authors: paschke e. Bioorg Med Chem Lett. 2017 Aug 1;27(15):3431-3435. doi: 10.1016/j.bmcl.2017.05.086. Epub 2017 May 30. Bioorg Med Chem Lett. 2017. PMID: 28600215
Unrelated CD3/CD19-depleted peripheral stem cell transplantation for Hurler syndrome.
Schwinger W, Sovinz P, Benesch M, Lackner H, Seidel M, Strenger V, Sperl D, Raicht A, Brunner-Krainz M, Paschke E, Plecko B, Urban C. Schwinger W, et al. Among authors: paschke e. Pediatr Hematol Oncol. 2014 Nov;31(8):723-30. doi: 10.3109/08880018.2014.939794. Epub 2014 Aug 12. Pediatr Hematol Oncol. 2014. PMID: 25116402
Pyridoxine responsiveness in novel mutations of the PNPO gene.
Plecko B, Paul K, Mills P, Clayton P, Paschke E, Maier O, Hasselmann O, Schmiedel G, Kanz S, Connolly M, Wolf N, Struys E, Stockler S, Abela L, Hofer D. Plecko B, et al. Among authors: paschke e. Neurology. 2014 Apr 22;82(16):1425-33. doi: 10.1212/WNL.0000000000000344. Epub 2014 Mar 21. Neurology. 2014. PMID: 24658933 Free PMC article.
Heparan sulfate levels in mucopolysaccharidoses and mucolipidoses.
Tomatsu S, Gutierrez MA, Ishimaru T, Peña OM, Montaño AM, Maeda H, Velez-Castrillon S, Nishioka T, Fachel AA, Cooper A, Thornley M, Wraith E, Barrera LA, Laybauer LS, Giugliani R, Schwartz IV, Frenking GS, Beck M, Kircher SG, Paschke E, Yamaguchi S, Ullrich K, Isogai K, Suzuki Y, Orii T, Noguchi A. Tomatsu S, et al. Among authors: paschke e. J Inherit Metab Dis. 2005;28(5):743-57. doi: 10.1007/s10545-005-0069-y. J Inherit Metab Dis. 2005. PMID: 16151906
Keratan sulphate levels in mucopolysaccharidoses and mucolipidoses.
Tomatsu S, Okamura K, Maeda H, Taketani T, Castrillon SV, Gutierrez MA, Nishioka T, Fachel AA, Orii KO, Grubb JH, Cooper A, Thornley M, Wraith E, Barrera LA, Laybauer LS, Giugliani R, Schwartz IV, Frenking GS, Beck M, Kircher SG, Paschke E, Yamaguchi S, Ullrich K, Haskins M, Isogai K, Suzuki Y, Orii T, Kondo N, Creer M, Okuyama T, Tanaka A, Noguchi A. Tomatsu S, et al. Among authors: paschke e. J Inherit Metab Dis. 2005;28(2):187-202. doi: 10.1007/s10545-005-5673-3. J Inherit Metab Dis. 2005. PMID: 15877208
98 results