Weydt P - Search Results

1

Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation.

Rona-Voros K, Eschbach J, Vernay A, Wiesner D, Schwalenstocker B, Geniquet P, Mousson De Camaret B, Echaniz-Laguna A, Loeffler JP, Ludolph AC, Weydt P, Dupuis L. Rona-Voros K, et al. Among authors: weydt p. Hum Mol Genet. 2013 Dec 20;22(25):5096-106. doi: 10.1093/hmg/ddt359. Epub 2013 Jul 29. Hum Mol Genet. 2013. PMID: 23900073

2

The role of PGC-1α in the pathogenesis of neurodegenerative disorders.

Róna-Vörös K, Weydt P. Róna-Vörös K, et al. Among authors: weydt p. Curr Drug Targets. 2010 Oct;11(10):1262-9. doi: 10.2174/1389450111007011262. Curr Drug Targets. 2010. PMID: 20840068 Review.

3

Progranulin bridges energy homeostasis and fronto-temporal dementia.

Dupuis L, Petersen A, Weydt P. Dupuis L, et al. Among authors: weydt p. Cell Metab. 2012 Mar 7;15(3):269-70; author reply 270. doi: 10.1016/j.cmet.2012.02.003. Cell Metab. 2012. PMID: 22405061 Free article. No abstract available.

4

Neuropathology of partial PGC-1α deficiency recapitulates features of mitochondrial encephalopathies but not of neurodegenerative diseases.

Szalardy L, Zadori D, Plangar I, Vecsei L, Weydt P, Ludolph AC, Klivenyi P, Kovacs GG. Szalardy L, et al. Among authors: weydt p. Neurodegener Dis. 2013;12(4):177-88. doi: 10.1159/000346267. Epub 2013 Feb 13. Neurodegener Dis. 2013. PMID: 23406886

5

PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis.

Eschbach J, Schwalenstöcker B, Soyal SM, Bayer H, Wiesner D, Akimoto C, Nilsson AC, Birve A, Meyer T, Dupuis L, Danzer KM, Andersen PM, Witting A, Ludolph AC, Patsch W, Weydt P. Eschbach J, et al. Among authors: weydt p. Hum Mol Genet. 2013 Sep 1;22(17):3477-84. doi: 10.1093/hmg/ddt202. Epub 2013 May 12. Hum Mol Genet. 2013. PMID: 23669350

6

Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.

Eschbach J, Sinniger J, Bouitbir J, Fergani A, Schlagowski AI, Zoll J, Geny B, René F, Larmet Y, Marion V, Baloh RH, Harms MB, Shy ME, Messadeq N, Weydt P, Loeffler JP, Ludolph AC, Dupuis L. Eschbach J, et al. Among authors: weydt p. Neurobiol Dis. 2013 Oct;58:220-30. doi: 10.1016/j.nbd.2013.05.015. Epub 2013 Jun 4. Neurobiol Dis. 2013. PMID: 23742762 Free PMC article.

7

Can lesions to the motor cortex induce amyotrophic lateral sclerosis?

Rosenbohm A, Kassubek J, Weydt P, Marroquin N, Volk AE, Kubisch C, Huppertz HJ, Weber M, Andersen PM, Weishaupt JH, Ludolph AC; ALS Schwaben Register Group. Rosenbohm A, et al. Among authors: weydt p. J Neurol. 2014 Feb;261(2):283-90. doi: 10.1007/s00415-013-7185-7. Epub 2013 Nov 20. J Neurol. 2014. PMID: 24253481

8

A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort.

Weydt P, Soyal SM, Landwehrmeyer GB, Patsch W; European Huntington Disease Network. Weydt P, et al. BMC Neurol. 2014 Jan 2;14:1. doi: 10.1186/1471-2377-14-1. BMC Neurol. 2014. PMID: 24383721 Free PMC article.

9

Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.

Lindenberg KS, Weydt P, Müller HP, Bornstedt A, Ludolph AC, Landwehrmeyer GB, Rottbauer W, Kassubek J, Rasche V. Lindenberg KS, et al. Among authors: weydt p. PLoS One. 2014 Aug 21;9(8):e105556. doi: 10.1371/journal.pone.0105556. eCollection 2014. PLoS One. 2014. PMID: 25144457 Free PMC article.

10

Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers.

Freischmidt A, Müller K, Zondler L, Weydt P, Volk AE, Božič AL, Walter M, Bonin M, Mayer B, von Arnim CA, Otto M, Dieterich C, Holzmann K, Andersen PM, Ludolph AC, Danzer KM, Weishaupt JH. Freischmidt A, et al. Among authors: weydt p. Brain. 2014 Nov;137(Pt 11):2938-50. doi: 10.1093/brain/awu249. Epub 2014 Sep 5. Brain. 2014. PMID: 25193138

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