Lamarche JB - Search Results

1

Somatic mosaicism for Friedreich's ataxia GAA triplet repeat expansions in the central nervous system.

Montermini L, Kish SJ, Jiralerspong S, Lamarche JB, Pandolfo M. Montermini L, et al. Among authors: lamarche jb. Neurology. 1997 Aug;49(2):606-10. doi: 10.1212/wnl.49.2.606. Neurology. 1997. PMID: 9270608

2

Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1.

Ross BM, Eder K, Moszczynska A, Mamalias N, Lamarche J, Ang L, Pandolfo M, Rouleau G, Kirchgessner M, Kish SJ. Ross BM, et al. Mov Disord. 2000 Mar;15(2):294-300. doi: 10.1002/1531-8257(200003)15:2<294::aid-mds1013>3.0.co;2-d. Mov Disord. 2000. PMID: 10752579

3

Immunoreactive levels of alpha-ketoglutarate dehydrogenase subunits in Friedreich's ataxia and spinocerebellar ataxia type 1.

Mastrogiacomo F, LaMarche J, Dozić S, Lindsay G, Bettendorff L, Robitaille Y, Schut L, Kish SJ. Mastrogiacomo F, et al. Neurodegeneration. 1996 Mar;5(1):27-33. doi: 10.1006/neur.1996.0004. Neurodegeneration. 1996. PMID: 8731379

4

Brain levels of thiamine and its phosphate esters in Friedreich's ataxia and spinocerebellar ataxia type 1.

Bettendorff L, Mastrogiacomo F, LaMarche J, Dozić S, Kish SJ. Bettendorff L, et al. Mov Disord. 1996 Jul;11(4):437-9. doi: 10.1002/mds.870110415. Mov Disord. 1996. PMID: 8813226

5

Decreased brain protein levels of cytochrome oxidase subunits in Alzheimer's disease and in hereditary spinocerebellar ataxia disorders: a nonspecific change?

Kish SJ, Mastrogiacomo F, Guttman M, Furukawa Y, Taanman JW, Dozić S, Pandolfo M, Lamarche J, DiStefano L, Chang LJ. Kish SJ, et al. J Neurochem. 1999 Feb;72(2):700-7. doi: 10.1046/j.1471-4159.1999.0720700.x. J Neurochem. 1999. PMID: 9930743 Free article.

6

Experimental allergic encephalomyelitis: a neurourological study.

Germain L, Galeano C, Lamarche J, Elhilali MM. Germain L, et al. Exp Neurol. 1988 Feb;99(2):239-46. doi: 10.1016/0014-4886(88)90144-6. Exp Neurol. 1988. PMID: 3338519

7

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

Nasreddine ZS, Loginov M, Clark LN, Lamarche J, Miller BL, Lamontagne A, Zhukareva V, Lee VM, Wilhelmsen KC, Geschwind DH. Nasreddine ZS, et al. Ann Neurol. 1999 Jun;45(6):704-15. doi: 10.1002/1531-8249(199906)45:6<704::aid-ana4>3.0.co;2-x. Ann Neurol. 1999. PMID: 10360762

8

Synapses in the hereditary ataxias.

Koeppen AH, Dickson AC, Lamarche JB, Robitaille Y. Koeppen AH, et al. Among authors: lamarche jb. J Neuropathol Exp Neurol. 1999 Jul;58(7):748-64. doi: 10.1097/00005072-199907000-00009. J Neuropathol Exp Neurol. 1999. PMID: 10411345

9

Iron and iron-responsive proteins in the cardiomyopathy of Friedreich's ataxia.

Michael S, Petrocine SV, Qian J, Lamarche JB, Knutson MD, Garrick MD, Koeppen AH. Michael S, et al. Among authors: lamarche jb. Cerebellum. 2006;5(4):257-67. doi: 10.1080/14734220600913246. Cerebellum. 2006. PMID: 17134988

10

The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins.

Koeppen AH, Michael SC, Knutson MD, Haile DJ, Qian J, Levi S, Santambrogio P, Garrick MD, Lamarche JB. Koeppen AH, et al. Among authors: lamarche jb. Acta Neuropathol. 2007 Aug;114(2):163-73. doi: 10.1007/s00401-007-0220-y. Epub 2007 Apr 11. Acta Neuropathol. 2007. PMID: 17443334 Free article.

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