Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
2006 2
2007 1
2011 2
2012 4
2013 2
2014 4
2015 2
2016 7
2017 3
2018 3
2019 6
2020 16
2021 10
2022 10
2023 7
2024 7

Text availability

Article attribute

Article type

Publication date

Search Results

73 results

Results by year

Filters applied: . Clear all
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.
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.
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.
Clinical Significance of Diffusion Tensor Imaging in Metachromatic Leukodystrophy.
Amedick LB, Martin P, Beschle J, Strölin M, Wilke M, Wolf N, Pouwels P, Hagberg G, Klose U, Naegele T, Kraegeloh-Mann I, Groeschel S. Amedick LB, et al. Among authors: groeschel s. Neuropediatrics. 2023 Aug;54(4):244-252. doi: 10.1055/a-2073-4178. Epub 2023 Apr 13. Neuropediatrics. 2023. PMID: 37054976 Free PMC article.
Predicting hand function after hemidisconnection.
Küpper H, Kudernatsch M, Pieper T, Groeschel S, Tournier JD, Raffelt D, Winkler P, Holthausen H, Staudt M. Küpper H, et al. Among authors: groeschel s. Brain. 2016 Sep;139(Pt 9):2456-68. doi: 10.1093/brain/aww170. Epub 2016 Jul 6. Brain. 2016. PMID: 27383529
Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes.
Laugwitz L, Seibt A, Herebian D, Peralta S, Kienzle I, Buchert R, Falb R, Gauck D, Müller A, Grimmel M, Beck-Woedel S, Kern J, Daliri K, Katibeh P, Danhauser K, Leiz S, Alesi V, Baertling F, Vasco G, Steinfeld R, Wagner M, Caglayan AO, Gumus H, Burmeister M, Mayatepek E, Martinelli D, Tamhankar PM, Tamhankar V, Joset P, Steindl K, Rauch A, Bonnen PE, Froukh T, Groeschel S, Krägeloh-Mann I, Haack TB, Distelmaier F. Laugwitz L, et al. Among authors: groeschel s. J Med Genet. 2022 Sep;59(9):878-887. doi: 10.1136/jmedgenet-2021-107729. Epub 2021 Oct 16. J Med Genet. 2022. PMID: 34656997 Free PMC article.
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
73 results