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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.
Therapies of lysosomal storage disorders targeting the brain.
Krägeloh-Mann I, Groeschel S. Krägeloh-Mann I, et al. Among authors: groeschel s. Lancet. 2016 Jul 30;388(10043):440-2. doi: 10.1016/S0140-6736(16)30450-0. Epub 2016 Jun 8. Lancet. 2016. PMID: 27289176 No abstract available.
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.
Cerebellar lesions in pediatric abusive head trauma.
Haas-Lude K, Roulet-Perez E, Döbler-Neumann M, Groeschel S, Nägele T, Krägeloh-Mann I. Haas-Lude K, et al. Among authors: groeschel s. Eur J Paediatr Neurol. 2019 Jul;23(4):604-608. doi: 10.1016/j.ejpn.2019.05.001. Epub 2019 May 17. Eur J Paediatr Neurol. 2019. PMID: 31147107
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.
79 results