Munz M - Search Results

1

Further delineation of the SATB2 phenotype.

Döcker D, Schubach M, Menzel M, Munz M, Spaich C, Biskup S, Bartholdi D. Döcker D, et al. Among authors: munz m. Eur J Hum Genet. 2014 Aug;22(8):1034-9. doi: 10.1038/ejhg.2013.280. Epub 2013 Dec 4. Eur J Hum Genet. 2014. PMID: 24301056 Free PMC article.

2

Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype.

Synofzik M, Maetzler W, Grehl T, Prudlo J, Vom Hagen JM, Haack T, Rebassoo P, Munz M, Schöls L, Biskup S. Synofzik M, et al. Among authors: munz m. Neurobiol Aging. 2012 Dec;33(12):2949.e13-7. doi: 10.1016/j.neurobiolaging.2012.07.002. Epub 2012 Aug 11. Neurobiol Aging. 2012. PMID: 22892309

3

GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?

Pilotto A, Schulte C, Hauser AK, Biskup S, Munz M, Brockmann K, Schaeffer E, Synofzik M, Maetzler W, Suenkel U, Srulijes K, Gasser T, Berg D. Pilotto A, et al. Among authors: munz m. Eur J Neurol. 2016 Mar;23(3):520-6. doi: 10.1111/ene.12894. Epub 2015 Nov 9. Eur J Neurol. 2016. PMID: 26549049

4

Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.

Krüger S, Battke F, Sprecher A, Munz M, Synofzik M, Schöls L, Gasser T, Grehl T, Prudlo J, Biskup S. Krüger S, et al. Among authors: munz m. Front Mol Neurosci. 2016 Oct 13;9:92. doi: 10.3389/fnmol.2016.00092. eCollection 2016. Front Mol Neurosci. 2016. PMID: 27790088 Free PMC article.

5

The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4.

Funk N, Munz M, Ott T, Brockmann K, Wenninger-Weinzierl A, Kühn R, Vogt-Weisenhorn D, Giesert F, Wurst W, Gasser T, Biskup S. Funk N, et al. Among authors: munz m. Sci Rep. 2019 Mar 14;9(1):4515. doi: 10.1038/s41598-019-40808-y. Sci Rep. 2019. PMID: 30872638 Free PMC article.

6

Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype.

Asmus F, Hjermind LE, Dupont E, Wagenstaller J, Haberlandt E, Munz M, Strom TM, Gasser T. Asmus F, et al. Among authors: munz m. Brain. 2007 Oct;130(Pt 10):2736-45. doi: 10.1093/brain/awm209. Brain. 2007. PMID: 17898012

7

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.

Fuchs J, Nilsson C, Kachergus J, Munz M, Larsson EM, Schüle B, Langston JW, Middleton FA, Ross OA, Hulihan M, Gasser T, Farrer MJ. Fuchs J, et al. Among authors: munz m. Neurology. 2007 Mar 20;68(12):916-22. doi: 10.1212/01.wnl.0000254458.17630.c5. Epub 2007 Jan 24. Neurology. 2007. PMID: 17251522

8

"Jerky" dystonia in children: spectrum of phenotypes and genetic testing.

Asmus F, Langseth A, Doherty E, Nestor T, Munz M, Gasser T, Lynch T, King MD. Asmus F, et al. Among authors: munz m. Mov Disord. 2009 Apr 15;24(5):702-9. doi: 10.1002/mds.22426. Mov Disord. 2009. PMID: 19117362

9

The transcription factor PITX3 is associated with sporadic Parkinson's disease.

Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wüllner U, Illig T, Sharma M, Gasser T. Fuchs J, et al. Among authors: munz m. Neurobiol Aging. 2009 May;30(5):731-8. doi: 10.1016/j.neurobiolaging.2007.08.014. Epub 2007 Oct 1. Neurobiol Aging. 2009. PMID: 17905480

10

Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.

Asmus F, Devlin A, Munz M, Zimprich A, Gasser T, Chinnery PF. Asmus F, et al. Among authors: munz m. Mov Disord. 2007 Oct 31;22(14):2104-9. doi: 10.1002/mds.21692. Mov Disord. 2007. PMID: 17702043

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

173 results

Search Page

Filters