Ludolph AC - Search Results

1

Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future.

Weydt P, Sagnelli A, Rosenbohm A, Fratta P, Pradat PF, Ludolph AC, Pareyson D. Weydt P, et al. Among authors: ludolph ac. J Mol Neurosci. 2016 Mar;58(3):379-87. doi: 10.1007/s12031-015-0682-7. Epub 2015 Nov 14. J Mol Neurosci. 2016. PMID: 26572537 Review.

2

Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study.

Kassubek J, Juengling FD, Hoffmann S, Rosenbohm A, Kurt A, Jurkat-Rott K, Steinbach P, Wolf M, Ludolph AC, Lehmann-Horn F, Lerche H, Weber YG. Kassubek J, et al. Among authors: ludolph ac. Neurosci Lett. 2003 Sep 11;348(2):73-6. doi: 10.1016/s0304-3940(03)00740-7. Neurosci Lett. 2003. PMID: 12902021

3

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

Münch C, Rosenbohm A, Sperfeld AD, Uttner I, Reske S, Krause BJ, Sedlmeier R, Meyer T, Hanemann CO, Stumm G, Ludolph AC. Münch C, et al. Among authors: ludolph ac. Ann Neurol. 2005 Nov;58(5):777-80. doi: 10.1002/ana.20631. Ann Neurol. 2005. PMID: 16240349

4

Classification of phenotype characteristics in adult-onset spinal muscular atrophy.

Gdynia HJ, Sperfeld AD, Flaith L, Kuehnlein P, Unrath A, Ludolph AC, Kassubek J. Gdynia HJ, et al. Among authors: ludolph ac. Eur Neurol. 2007;58(3):170-6. doi: 10.1159/000104719. Epub 2007 Jun 29. Eur Neurol. 2007. PMID: 17622724

5

Frontotemporal cognitive function in X-linked spinal and bulbar muscular atrophy (SBMA): a controlled neuropsychological study of 20 patients.

Soukup GR, Sperfeld AD, Uttner I, Karitzky J, Ludolph AC, Kassubek J, Schreiber H. Soukup GR, et al. Among authors: ludolph ac. J Neurol. 2009 Nov;256(11):1869-75. doi: 10.1007/s00415-009-5212-5. Epub 2009 Jul 2. J Neurol. 2009. PMID: 19572162

6

Guidelines for preclinical animal research in ALS/MND: A consensus meeting.

Ludolph AC, Bendotti C, Blaugrund E, Chio A, Greensmith L, Loeffler JP, Mead R, Niessen HG, Petri S, Pradat PF, Robberecht W, Ruegg M, Schwalenstöcker B, Stiller D, van den Berg L, Vieira F, von Horsten S. Ludolph AC, et al. Amyotroph Lateral Scler. 2010;11(1-2):38-45. doi: 10.3109/17482960903545334. Amyotroph Lateral Scler. 2010. PMID: 20184514

7

Energy metabolism in amyotrophic lateral sclerosis.

Dupuis L, Pradat PF, Ludolph AC, Loeffler JP. Dupuis L, et al. Among authors: ludolph ac. Lancet Neurol. 2011 Jan;10(1):75-82. doi: 10.1016/S1474-4422(10)70224-6. Epub 2010 Oct 27. Lancet Neurol. 2011. PMID: 21035400 Review.

8

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: ludolph ac. Neurodegener Dis. 2013;12(4):177-88. doi: 10.1159/000346267. Epub 2013 Feb 13. Neurodegener Dis. 2013. PMID: 23406886

9

Implementation of a population-based epidemiological rare disease registry: study protocol of the amyotrophic lateral sclerosis (ALS)--registry Swabia.

Nagel G, Unal H, Rosenbohm A, Ludolph AC, Rothenbacher D; ALS Registry Study Group. Nagel G, et al. Among authors: ludolph ac. BMC Neurol. 2013 Feb 17;13:22. doi: 10.1186/1471-2377-13-22. BMC Neurol. 2013. PMID: 23414001 Free PMC article.

10

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: ludolph ac. 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

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