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Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1.
Eder K, Kish SJ, Kirchgessner M, Ross BM. Eder K, et al. Among authors: kish sj. Mov Disord. 1998 Sep;13(5):813-9. doi: 10.1002/mds.870130510. Mov Disord. 1998. PMID: 9756151
Nigral glutathione deficiency is not specific for idiopathic Parkinson's disease.
Fitzmaurice PS, Ang L, Guttman M, Rajput AH, Furukawa Y, Kish SJ. Fitzmaurice PS, et al. Among authors: kish sj. Mov Disord. 2003 Sep;18(9):969-76. doi: 10.1002/mds.10486. Mov Disord. 2003. PMID: 14502663
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. Among authors: kish sj. Mov Disord. 2000 Mar;15(2):294-300. doi: 10.1002/1531-8257(200003)15:2<294::aid-mds1013>;2-d. Mov Disord. 2000. PMID: 10752579
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
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. Among authors: kish sj. Mov Disord. 1996 Jul;11(4):437-9. doi: 10.1002/mds.870110415. Mov Disord. 1996. PMID: 8813226
Brain acetylcholinesterase activity is markedly reduced in dominantly-inherited olivopontocerebellar atrophy.
Kish SJ, Schut L, Simmons J, Gilbert J, Chang LJ, Rebbetoy M. Kish SJ, et al. J Neurol Neurosurg Psychiatry. 1988 Apr;51(4):544-8. doi: 10.1136/jnnp.51.4.544. J Neurol Neurosurg Psychiatry. 1988. PMID: 3164041 Free PMC article.
Neuropsychological test performance in patients with dominantly inherited spinocerebellar ataxia: relationship to ataxia severity.
Kish SJ, el-Awar M, Stuss D, Nobrega J, Currier R, Aita JF, Schut L, Zoghbi HY, Freedman M. Kish SJ, et al. Neurology. 1994 Sep;44(9):1738-46. doi: 10.1212/wnl.44.9.1738. Neurology. 1994. PMID: 7936307
Cerebellar alpha-ketoglutarate dehydrogenase activity is reduced in spinocerebellar ataxia type 1.
Mastrogiacomo F, Kish SJ. Mastrogiacomo F, et al. Among authors: kish sj. Ann Neurol. 1994 May;35(5):624-6. doi: 10.1002/ana.410350519. Ann Neurol. 1994. PMID: 7910005
Striatal dihydroxyphenylalanine decarboxylase and tyrosine hydroxylase protein in idiopathic Parkinson's disease and dominantly inherited olivopontocerebellar atrophy.
Zhong XH, Haycock JW, Shannak K, Robitaille Y, Fratkin J, Koeppen AH, Hornykiewicz O, Kish SJ. Zhong XH, et al. Among authors: kish sj. Mov Disord. 1995 Jan;10(1):10-7. doi: 10.1002/mds.870100104. Mov Disord. 1995. PMID: 7885342
Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy.
Kish SJ, Currier RD, Schut L, Perry TL, Morito CL. Kish SJ, et al. Ann Neurol. 1987 Aug;22(2):272-5. doi: 10.1002/ana.410220214. Ann Neurol. 1987. PMID: 3477997
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