Synofzik M - Search Results

1

Delineating MT-ATP6-associated disease: From isolated neuropathy to early onset neurodegeneration.

Stendel C, Neuhofer C, Floride E, Yuqing S, Ganetzky RD, Park J, Freisinger P, Kornblum C, Kleinle S, Schöls L, Distelmaier F, Stettner GM, Büchner B, Falk MJ, Mayr JA, Synofzik M, Abicht A, Haack TB, Prokisch H, Wortmann SB, Murayama K, Fang F, Klopstock T; ATP6 Study Group. Stendel C, et al. Among authors: synofzik m. Neurol Genet. 2020 Jan 13;6(1):e393. doi: 10.1212/NXG.0000000000000393. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042921 Free PMC article.

2

Prion mutation D178N with highly variable disease onset and phenotype.

Synofzik M, Bauer P, Schöls L. Synofzik M, et al. J Neurol Neurosurg Psychiatry. 2009 Mar;80(3):345-6. doi: 10.1136/jnnp.2008.149922. J Neurol Neurosurg Psychiatry. 2009. PMID: 19228673

3

Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations.

Schulte C, Synofzik M, Gasser T, Schöls L. Schulte C, et al. Among authors: synofzik m. Neurology. 2009 Sep 15;73(11):898-900. doi: 10.1212/WNL.0b013e3181b78488. Neurology. 2009. PMID: 19752458 No abstract available.

4

Intensive coordinative training improves motor performance in degenerative cerebellar disease.

Ilg W, Synofzik M, Brötz D, Burkard S, Giese MA, Schöls L. Ilg W, et al. Among authors: synofzik m. Neurology. 2009 Dec 1;73(22):1823-30. doi: 10.1212/WNL.0b013e3181c33adf. Epub 2009 Oct 28. Neurology. 2009. PMID: 19864636 Clinical Trial.

5

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia.

Schüle R, Schlipf N, Synofzik M, Klebe S, Klimpe S, Hehr U, Winner B, Lindig T, Dotzer A, Riess O, Winkler J, Schöls L, Bauer P. Schüle R, et al. Among authors: synofzik m. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1402-4. doi: 10.1136/jnnp.2008.167528. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917823

6

The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosis.

Synofzik M, Fernández-Santiago R, Maetzler W, Schöls L, Andersen PM. Synofzik M, et al. J Neurol Neurosurg Psychiatry. 2010 Jul;81(7):764-7. doi: 10.1136/jnnp.2009.181719. Epub 2010 Feb 22. J Neurol Neurosurg Psychiatry. 2010. PMID: 20176600

7

Severe orthostatic dysregulation associated with Wolfram syndrome.

Synofzik M, Weiss D, Erharhaghen J, Krüger R, Schöls L. Synofzik M, et al. J Neurol. 2010 Oct;257(10):1751-3. doi: 10.1007/s00415-010-5593-5. Epub 2010 May 19. J Neurol. 2010. PMID: 20490821 No abstract available.

8

Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds.

Bauer P, Stevanin G, Beetz C, Synofzik M, Schmitz-Hübsch T, Wüllner U, Berthier E, Ollagnon-Roman E, Riess O, Forlani S, Mundwiller E, Durr A, Schöls L, Brice A. Bauer P, et al. Among authors: synofzik m. J Neurol Neurosurg Psychiatry. 2010 Nov;81(11):1229-32. doi: 10.1136/jnnp.2009.202150. Epub 2010 Jul 28. J Neurol Neurosurg Psychiatry. 2010. PMID: 20667868

9

Long-term effects of coordinative training in degenerative cerebellar disease.

Ilg W, Brötz D, Burkard S, Giese MA, Schöls L, Synofzik M. Ilg W, et al. Among authors: synofzik m. Mov Disord. 2010 Oct 15;25(13):2239-46. doi: 10.1002/mds.23222. Mov Disord. 2010. PMID: 20737551 Clinical Trial.

10

POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe.

Schicks J, Synofzik M, Schulte C, Schöls L. Schicks J, et al. Among authors: synofzik m. Mov Disord. 2010 Nov 15;25(15):2678-82. doi: 10.1002/mds.23286. Mov Disord. 2010. PMID: 20803511

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