Zimmermann M - Search Results

1

FIG4 mutations leading to parkinsonism and a phenotypical continuum between CMT4J and Yunis Varón syndrome.

Zimmermann M, Schuster S, Boesch S, Korenke GC, Mohr J, Reichbauer J, Kernstock C, Kotzot D, Spahlinger V, Schüle-Freyer R, Schöls L. Zimmermann M, et al. Parkinsonism Relat Disord. 2020 May;74:6-11. doi: 10.1016/j.parkreldis.2020.03.021. Epub 2020 Mar 28. Parkinsonism Relat Disord. 2020. PMID: 32268254

2

Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism.

Zimmermann M, Wilke C, Schulte C, Hoffmann J, Klopfer J, Reimold M, Brockmann K, Synofzik M. Zimmermann M, et al. Parkinsonism Relat Disord. 2018 Oct;55:145-147. doi: 10.1016/j.parkreldis.2018.06.006. Epub 2018 Jun 6. Parkinsonism Relat Disord. 2018. PMID: 29910155 No abstract available.

3

Serum neurofilament light chain is increased in hereditary spastic paraplegias.

Wilke C, Rattay TW, Hengel H, Zimmermann M, Brockmann K, Schöls L, Kuhle J, Schüle R, Synofzik M. Wilke C, et al. Among authors: zimmermann m. Ann Clin Transl Neurol. 2018 May 21;5(7):876-882. doi: 10.1002/acn3.583. eCollection 2018 Jul. Ann Clin Transl Neurol. 2018. PMID: 30009206 Free PMC article.

4

Seroprevalence of autoimmune antibodies in degenerative ataxias: a broad, disease-controlled screening in 456 subjects.

Roeben B, Scharf M, Miske R, Teegen B, Traschütz A, Wilke C, Zimmermann M, Deuschle C, Schulte C, Brockmann K, Schöls L, Komorowski L, Synofzik M. Roeben B, et al. Among authors: zimmermann m. J Neurol. 2023 Nov;270(11):5649-5654. doi: 10.1007/s00415-023-11900-1. Epub 2023 Jul 28. J Neurol. 2023. PMID: 37507501 Free PMC article. No abstract available.

5

Parkinson's Disease: Glucocerebrosidase 1 Mutation Severity Is Associated with CSF Alpha-Synuclein Profiles.

Lerche S, Wurster I, Roeben B, Zimmermann M, Riebenbauer B, Deuschle C, Hauser AK, Schulte C, Berg D, Maetzler W, Waniek K, Lachmann I, Liepelt-Scarfone I, Gasser T, Brockmann K. Lerche S, et al. Among authors: zimmermann m. Mov Disord. 2020 Mar;35(3):495-499. doi: 10.1002/mds.27884. Epub 2019 Oct 30. Mov Disord. 2020. PMID: 31670439

6

Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosis.

Zimmermann M, Deininger N, Willikens S, Haack TB, Grundmann-Hauser K, Streubel B, Schreiber M, Lerche H, Grimm A. Zimmermann M, et al. Neurol Sci. 2021 Apr;42(4):1523-1525. doi: 10.1007/s10072-020-04896-3. Epub 2020 Nov 13. Neurol Sci. 2021. PMID: 33188503 Free PMC article.

7

Patient's perception: shorter and more severe prodromal phase in GBA-associated PD.

Zimmermann M, Gaenslen A, Prahl K, Srulijes K, Hauser AK, Schulte C, Csoti I, Berg D, Brockmann K. Zimmermann M, et al. Eur J Neurol. 2019 Apr;26(4):694-698. doi: 10.1111/ene.13776. Epub 2018 Sep 14. Eur J Neurol. 2019. PMID: 30107068

8

Polygenic load: Earlier disease onset but similar longitudinal progression in Parkinson's disease.

Lerche S, Liepelt-Scarfone I, Wurster I, Schulte C, Schäffer E, Röben B, Machetanz G, Zimmermann M, Akbas S, Hauser AK, Gasser T, Maetzler W, Berg D, Brockmann K. Lerche S, et al. Among authors: zimmermann m. Mov Disord. 2018 Aug;33(8):1349-1353. doi: 10.1002/mds.27427. Epub 2018 Aug 22. Mov Disord. 2018. PMID: 30132985

9

The longevity gene Klotho and its cerebrospinal fluid protein profiles as a modifier for Parkinson´s disease.

Zimmermann M, Köhler L, Kovarova M, Lerche S, Schulte C, Wurster I, Machetanz G, Deuschle C, Hauser AK, Gasser T, Berg D, Schleicher E, Maetzler W, Brockmann K. Zimmermann M, et al. Eur J Neurol. 2021 May;28(5):1557-1565. doi: 10.1111/ene.14733. Epub 2021 Feb 6. Eur J Neurol. 2021. PMID: 33449400

10

The Mutation Matters: CSF Profiles of GCase, Sphingolipids, α-Synuclein in PD_GBA.

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: zimmermann m. Mov Disord. 2021 May;36(5):1216-1228. doi: 10.1002/mds.28472. Epub 2021 Feb 6. Mov Disord. 2021. PMID: 33547828

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