Karpati G - Search Results

1

Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositis.

Mezei MM, Mankodi A, Brais B, Marineau C, Thornton CA, Rouleau GA, Karpati G. Mezei MM, et al. Among authors: karpati g. Neurology. 1999 Feb;52(3):669-70. doi: 10.1212/wnl.52.3.669. Neurology. 1999. PMID: 10025815 No abstract available.

2

Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice.

Dion P, Shanmugam V, Gaspar C, Messaed C, Meijer I, Toulouse A, Laganiere J, Roussel J, Rochefort D, Laganiere S, Allen C, Karpati G, Bouchard JP, Brais B, Rouleau GA. Dion P, et al. Among authors: karpati g. Neurobiol Dis. 2005 Apr;18(3):528-36. doi: 10.1016/j.nbd.2004.09.021. Neurobiol Dis. 2005. PMID: 15755680

3

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.

Dupré N, Howard HC, Mathieu J, Karpati G, Vanasse M, Bouchard JP, Carpenter S, Rouleau GA. Dupré N, et al. Among authors: karpati g. Ann Neurol. 2003 Jul;54(1):9-18. doi: 10.1002/ana.77777. Ann Neurol. 2003. PMID: 12838516 Review.

4

HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.

Fan X, Messaed C, Dion P, Laganiere J, Brais B, Karpati G, Rouleau GA. Fan X, et al. Among authors: karpati g. Can J Neurol Sci. 2003 Aug;30(3):244-51. doi: 10.1017/s0317167100002675. Can J Neurol Sci. 2003. PMID: 12945950

5

PABPN1 overexpression leads to upregulation of genes encoding nuclear proteins that are sequestered in oculopharyngeal muscular dystrophy nuclear inclusions.

Corbeil-Girard LP, Klein AF, Sasseville AM, Lavoie H, Dicaire MJ, Saint-Denis A, Pagé M, Duranceau A, Codère F, Bouchard JP, Karpati G, Rouleau GA, Massie B, Langelier Y, Brais B. Corbeil-Girard LP, et al. Among authors: karpati g. Neurobiol Dis. 2005 Apr;18(3):551-67. doi: 10.1016/j.nbd.2004.10.019. Neurobiol Dis. 2005. PMID: 15755682

6

Sporadic inclusion body myositis: pathogenic considerations.

Karpati G, O'Ferrall EK. Karpati G, et al. Ann Neurol. 2009 Jan;65(1):7-11. doi: 10.1002/ana.21622. Ann Neurol. 2009. PMID: 19194875 Review.

7

Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis.

Horvath R, Fu K, Johns T, Genge A, Karpati G, Shoubridge EA. Horvath R, et al. Among authors: karpati g. J Neuropathol Exp Neurol. 1998 May;57(5):396-403. doi: 10.1097/00005072-199805000-00003. J Neuropathol Exp Neurol. 1998. PMID: 9596410

8

Familial inclusion body myositis among Kurdish-Iranian Jews.

Massa R, Weller B, Karpati G, Shoubridge E, Carpenter S. Massa R, et al. Among authors: karpati g. Arch Neurol. 1991 May;48(5):519-22. doi: 10.1001/archneur.1991.00530170083024. Arch Neurol. 1991. PMID: 1850594

9

Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. A new syndrome.

Cole AJ, Kuzniecky R, Karpati G, Carpenter S, Andermann E, Andermann F. Cole AJ, et al. Among authors: karpati g. Brain. 1988 Oct;111 ( Pt 5):1025-37. doi: 10.1093/brain/111.5.1025. Brain. 1988. PMID: 2846114

10

Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy.

Sinnreich M, Therrien C, Karpati G. Sinnreich M, et al. Among authors: karpati g. Neurology. 2006 Apr 11;66(7):1114-6. doi: 10.1212/01.wnl.0000204358.89303.81. Neurology. 2006. PMID: 16606933

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