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

Year Number of Results
2006 2
2007 1
2010 1
2011 2
2012 5
2013 3
2014 4
2015 4
2016 6
2017 4
2018 2
2019 6
2020 16
2021 10
2022 7
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61 results
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Page 1
The European Reference Network for Rare Neurological Diseases.
Reinhard C, Bachoud-Lévi AC, Bäumer T, Bertini E, Brunelle A, Buizer AI, Federico A, Gasser T, Groeschel S, Hermanns S, Klockgether T, Krägeloh-Mann I, Landwehrmeyer GB, Leber I, Macaya A, Mariotti C, Meissner WG, Molnar MJ, Nonnekes J, Ortigoza Escobar JD, Pérez Dueñas B, Renna Linton L, Schöls L, Schuele R, Tijssen MAJ, Vandenberghe R, Volkmer A, Wolf NI, Graessner H. Reinhard C, et al. Among authors: groeschel s. Front Neurol. 2021 Jan 14;11:616569. doi: 10.3389/fneur.2020.616569. eCollection 2020. Front Neurol. 2021. PMID: 33519696 Free PMC article. Review.
[Lysosomal storage diseases].
Schulze M, Groeschel S, Gburek-Augustat J, Nägele T, Horger M. Schulze M, et al. Among authors: groeschel s. Rofo. 2015 Dec;187(12):1057-60. doi: 10.1055/s-0035-1552368. Epub 2015 Nov 26. Rofo. 2015. PMID: 26609772 German. No abstract available.
Intravenous arylsulfatase A in metachromatic leukodystrophy: a phase 1/2 study.
Í Dali C, Groeschel S, Moldovan M, Farah MH, Krägeloh-Mann I, Wasilewski M, Li J, Barton N, Krarup C. Í Dali C, et al. Among authors: groeschel s. Ann Clin Transl Neurol. 2021 Jan;8(1):66-80. doi: 10.1002/acn3.51254. Epub 2020 Dec 17. Ann Clin Transl Neurol. 2021. PMID: 33332761 Free PMC article. Clinical Trial.
Clinical application of advanced MR methods in children: points to consider.
Wilke M, Groeschel S, Lorenzen A, Rona S, Schuhmann MU, Ernemann U, Krägeloh-Mann I. Wilke M, et al. Among authors: groeschel s. Ann Clin Transl Neurol. 2018 Sep 27;5(11):1434-1455. doi: 10.1002/acn3.658. eCollection 2018 Nov. Ann Clin Transl Neurol. 2018. PMID: 30480038 Free PMC article. Review.
A connectome-based approach to assess motor outcome after neonatal arterial ischemic stroke.
Al Harrach M, Pretzel P, Groeschel S, Rousseau F, Dhollander T, Hertz-Pannier L, Lefevre J, Chabrier S, Dinomais M; AVCnn study group. Al Harrach M, et al. Among authors: groeschel s. Ann Clin Transl Neurol. 2021 May;8(5):1024-1037. doi: 10.1002/acn3.51292. Epub 2021 Mar 30. Ann Clin Transl Neurol. 2021. PMID: 33787079 Free PMC article.
Phenotypic variation between siblings with Metachromatic Leukodystrophy.
Elgün S, Waibel J, Kehrer C, van Rappard D, Böhringer J, Beck-Wödl S, Just J, Schöls L, Wolf N, Krägeloh-Mann I, Groeschel S. Elgün S, et al. Among authors: groeschel s. Orphanet J Rare Dis. 2019 Jun 11;14(1):136. doi: 10.1186/s13023-019-1113-6. Orphanet J Rare Dis. 2019. PMID: 31186049 Free PMC article.
61 results