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

Year Number of Results
1995 1
1996 1
1997 1
2010 1
2012 1
2016 1
2017 4
2018 2
2019 3
2020 4
2021 4
2022 5
2023 0
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23 results
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Page 1
A Mutation-Agnostic Hematopoietic Stem Cell Gene Therapy for Metachromatic Leukodystrophy.
Antony JS, Daniel-Moreno A, Lamsfus-Calle A, Raju J, Kaftancioglu M, Ureña-Bailén G, Rottenberger J, Hou Y, Santhanakumaran V, Lee JH, Heumos L, Böhringer J, Krägeloh-Mann I, Handgretinger R, Mezger M. Antony JS, et al. Among authors: bohringer j. CRISPR J. 2022 Feb;5(1):66-79. doi: 10.1089/crispr.2021.0075. Epub 2021 Dec 8. CRISPR J. 2022. PMID: 34882002
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: bohringer j. 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.
Hematopoietic Stem Cell Transplantation with Mesenchymal Stromal Cells in Children with Metachromatic Leukodystrophy.
Cabanillas Stanchi KM, Böhringer J, Strölin M, Groeschel S, Lenglinger K, Treuner C, Kehrer C, Laugwitz L, Bevot A, Kaiser N, Schumm M, Lang P, Handgretinger R, Krägeloh-Mann I, Müller I, Döring M. Cabanillas Stanchi KM, et al. Among authors: bohringer j. Stem Cells Dev. 2022 Apr;31(7-8):163-175. doi: 10.1089/scd.2021.0352. Stem Cells Dev. 2022. PMID: 35323019
Identification of neurodegeneration indicators and disease progression in metachromatic leukodystrophy using quantitative NMR-based urinary metabolomics.
Laugwitz L, Zizmare L, Santhanakumaran V, Cannet C, Böhringer J, Okun JG, Spraul M, Krägeloh-Mann I, Groeschel S, Trautwein C. Laugwitz L, et al. Among authors: bohringer j. JIMD Rep. 2022 Jan 27;63(2):168-180. doi: 10.1002/jmd2.12273. eCollection 2022 Mar. JIMD Rep. 2022. PMID: 35281658 Free PMC article.
The Mutation Matters: CSF Profiles of GCase, Sphingolipids, α-Synuclein in PDGBA.
Lerche S, Schulte C, Wurster I, Machetanz G, Roeben B, Zimmermann M, Deuschle C, Hauser AK, Böhringer J, Krägeloh-Mann I, Waniek K, Lachmann I, Petterson XT, Chiang R, Park H, Wang B, Liepelt-Scarfone I, Maetzler W, Galasko D, Scherzer CR, Gasser T, Mielke MM, Hutten SJ, Mollenhauer B, Sardi SP, Berg D, Brockmann K. Lerche S, et al. Among authors: bohringer j. Mov Disord. 2021 May;36(5):1216-1228. doi: 10.1002/mds.28472. Epub 2021 Feb 6. Mov Disord. 2021. PMID: 33547828
Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency.
Brackmann F, Kehrer C, Kustermann W, Böhringer J, Krägeloh-Mann I, Trollmann R. Brackmann F, et al. Among authors: bohringer j. Neuropediatrics. 2017 Apr;48(2):127-130. doi: 10.1055/s-0037-1598646. Epub 2017 Feb 13. Neuropediatrics. 2017. PMID: 28192816
23 results