Zimmermann M - Search Results

1

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.

2

Frequency and neuropathology of HTT repeat expansions in FTD/ALS: co-existence rather than causation.

Zimmermann M, Mengel D, Raupach K, Haack T, Neumann M, Synofzik M. Zimmermann M, et al. J Neurol. 2024 Dec 12;272(1):58. doi: 10.1007/s00415-024-12822-2. J Neurol. 2024. PMID: 39666103 Free PMC article.

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

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

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

CSF NFL in a Longitudinally Assessed PD Cohort: Age Effects and Cognitive Trajectories.

Lerche S, Wurster I, Röben B, Zimmermann M, Machetanz G, Wiethoff S, Dehnert M, Rietschel L, Riebenbauer B, Deuschle C, Stransky E, Lieplt-Scarfone I, Gasser T, Brockmann K. Lerche S, et al. Among authors: zimmermann m. Mov Disord. 2020 Jul;35(7):1138-1144. doi: 10.1002/mds.28056. Epub 2020 May 23. Mov Disord. 2020. PMID: 32445500

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

Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha-synuclein profile.

Lerche S, Machetanz G, Wurster I, Roeben B, Zimmermann M, Pilotto A, Preische O, Stransky E, Deuschle C, Hauser AK, Schulte C, Lachmann I, Waniek K, Gasser T, Berg D, Maetzler W, Brockmann K. Lerche S, et al. Among authors: zimmermann m. Mov Disord. 2019 Jul;34(7):1069-1073. doi: 10.1002/mds.27731. Epub 2019 Jun 12. Mov Disord. 2019. PMID: 31189032

10

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

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