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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
2024 0

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97 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.
Anderson-Fabry disease in Austria.
Lorenz M, Hauser AC, Püspök-Schwarz M, Kotanko P, Arias I, Zodl H, Kramar R, Paschke E, Voigtländer T, Sunder-Plassmann G. Lorenz M, et al. Among authors: paschke e. Wien Klin Wochenschr. 2003 Apr 30;115(7-8):235-40. doi: 10.1007/BF03040321. Wien Klin Wochenschr. 2003. PMID: 12778775
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
Recurrent acroparaesthesia during febrile infections.
Bodamer OA, Ratschmann R, Paschke E, Voigtländer T, Stöckler-Ipsiroglu S. Bodamer OA, et al. Among authors: paschke e. Lancet. 2004 May 22;363(9422):1698. doi: 10.1016/S0140-6736(04)16254-5. Lancet. 2004. PMID: 15158631 No abstract available.
Another unusual case of fucosidosis.
Böck A, Fang-Kircher S, Braun F, Gerdov C, Breier F, Jurecka W, Paschke E. Böck A, et al. Among authors: paschke e. J Inherit Metab Dis. 1995;18(1):93-4. doi: 10.1007/BF00711388. J Inherit Metab Dis. 1995. PMID: 7623457 No abstract available.
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.
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
97 results