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Results: 1-11 |
Results: 11
CONSEQUENCES OF AGING ON MITOCHONDRIAL RESPIRATORY-CHAIN ENZYMES IN CULTURED HUMAN FIBROBLASTS TREATED WITH ASCORBATE
Authors: SHARMA P RUPAR CA RIP JW
Citation: P. Sharma et al., CONSEQUENCES OF AGING ON MITOCHONDRIAL RESPIRATORY-CHAIN ENZYMES IN CULTURED HUMAN FIBROBLASTS TREATED WITH ASCORBATE, Gerontology, 44(2), 1998, pp. 78-84
ASPARTYLGLUCOSAMINURIA IN A CANADIAN FAMILY
Authors: GORDON BA RUPAR CA RIP JW HAUST MD COULTERMACKIE MB SCOTT E HINTON GG
Citation: Ba. Gordon et al., ASPARTYLGLUCOSAMINURIA IN A CANADIAN FAMILY, Clinical and investigative medicine, 21(3), 1998, pp. 114-123
A 9 NT DELETION IN MT DNA IN 2 SIBLINGS WITH PERVASIVE DEVELOPMENTAL DISORDER (PDD) AND MITOCHONDRIAL MYOPATHY
Authors: RUPAR CA GORDON BA KRONICK JB LEVIN SD RAMSAY DA FOX M SZATMARI P
Citation: Ca. Rupar et al., A 9 NT DELETION IN MT DNA IN 2 SIBLINGS WITH PERVASIVE DEVELOPMENTAL DISORDER (PDD) AND MITOCHONDRIAL MYOPATHY, American journal of human genetics, 61(4), 1997, pp. 1867-1867
ISOLATED SULFITE OXIDASE DEFICIENCY
Authors: RUPAR CA GILLETT J GORDON BA RAMSAY DA JOHNSON JL GARRETT RM RAJAGOPALAN KV JUNG JH BACHEYIE GS SELLERS AR
Citation: Ca. Rupar et al., ISOLATED SULFITE OXIDASE DEFICIENCY, Neuropediatrics, 27(6), 1996, pp. 299-304
HETEROALLELIC MISSENSE MUTATIONS OF THE GALACTOSAMINE-B-SULFATE SULFATASE (GALNS) GENE IN A MILD FORM OF MORQUIO-DISEASE (MPS IVA)
Authors: COLE DEC FUKUDA S GORDON BA RIP JW LECOUTEUR AN RUPAR CA TOMATSU S OGAWA T SUKEGAWA K ORII T
Citation: Dec. Cole et al., HETEROALLELIC MISSENSE MUTATIONS OF THE GALACTOSAMINE-B-SULFATE SULFATASE (GALNS) GENE IN A MILD FORM OF MORQUIO-DISEASE (MPS IVA), American journal of medical genetics, 63(4), 1996, pp. 558-565
MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IS NOT A CAUSE OF PREVIOUSLY DIAGNOSED REYE SYNDROME
Authors: RUPAR CA FREWEN TW GORDON BA
Citation: Ca. Rupar et al., MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY IS NOT A CAUSE OF PREVIOUSLY DIAGNOSED REYE SYNDROME, Journal of inherited metabolic disease, 18(3), 1995, pp. 365-366
LETHAL MUSCLE COMPLEX-III DEFECT IN 2 INFANT SIBLINGS
Authors: KRONICK JB GORDON BA RUPAR CA RAMSAY DA ARMSTRONG RF
Citation: Jb. Kronick et al., LETHAL MUSCLE COMPLEX-III DEFECT IN 2 INFANT SIBLINGS, American journal of human genetics, 57(4), 1995, pp. 1035-1035
MITOCHONDRIAL-LIPID-GLYCOGEN STORAGE MYOPATHY WITH PROGRESSIVE LOSS OF RESPIRATORY-CHAIN COMPLEX-I, COMPLEX-II, COMPLEX-III AND COMPLEX-IV
Authors: RUPAR CA GILLETT J RAMSAY DA GORDON BA
Citation: Ca. Rupar et al., MITOCHONDRIAL-LIPID-GLYCOGEN STORAGE MYOPATHY WITH PROGRESSIVE LOSS OF RESPIRATORY-CHAIN COMPLEX-I, COMPLEX-II, COMPLEX-III AND COMPLEX-IV, American journal of human genetics, 57(4), 1995, pp. 1048-1048
NERVE BIOPSY FINDINGS IN NIEMANN-PICK TYPE-II (NPC)
Authors: HAHN AF GILBERT JJ KWARCIAK C GILLETT J BOLTON CF RUPAR CA CALLAHAN JW
Citation: Af. Hahn et al., NERVE BIOPSY FINDINGS IN NIEMANN-PICK TYPE-II (NPC), Acta Neuropathologica, 87(2), 1994, pp. 149-154
RETROSPECTIVE DIAGNOSIS OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY
Authors: CHRISTODOULOU J CLARKE JTR RUPAR CA GORDON BA KELLY DP
Citation: J. Christodoulou et al., RETROSPECTIVE DIAGNOSIS OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY, Journal of paediatrics and child health, 29(3), 1993, pp. 237-238
NERVE BIOPSY FINDINGS IN NIEMANN-PICK DISEASE TYPE-II
Authors: HAHN AF GILBERT JJ KWARCIAK C GILLETT J RUPAR CA CALLAHAN JW BOLTON CF
Citation: Af. Hahn et al., NERVE BIOPSY FINDINGS IN NIEMANN-PICK DISEASE TYPE-II, Annals of neurology, 34(2), 1993, pp. 269-269
Risultati: 1-11 |