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Results: 1-18 |
Results: 18
POLARIMETRIC METHOD FOR ICE WATER-CONTENT DETERMINATION
Authors: RYZHKOV AV ZRNIC DS GORDON BA
Citation: Av. Ryzhkov et al., POLARIMETRIC METHOD FOR ICE WATER-CONTENT DETERMINATION, Journal of applied meteorology, 37(2), 1998, pp. 125-134
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 SIMPLE SPECTROPHOTOMETRIC ENZYME ASSAY WITH ABSOLUTE SPECIFICITY FOR ARYLSULFATASE-A
Authors: RIP JW GORDON BA
Citation: Jw. Rip et Ba. Gordon, A SIMPLE SPECTROPHOTOMETRIC ENZYME ASSAY WITH ABSOLUTE SPECIFICITY FOR ARYLSULFATASE-A, Clinical biochemistry, 31(1), 1998, pp. 29-31
WHOLE-BODY POSITRON-EMISSION-TOMOGRAPHY - NORMAL VARIATIONS, PITFALLS, AND TECHNICAL CONSIDERATIONS
Authors: GORDON BA FLANAGAN FL DEHDASHTI F
Citation: Ba. Gordon et al., WHOLE-BODY POSITRON-EMISSION-TOMOGRAPHY - NORMAL VARIATIONS, PITFALLS, AND TECHNICAL CONSIDERATIONS, American journal of roentgenology, 169(6), 1997, pp. 1675-1680
COMPARISON OF FDG-PET AND INTRAOPERATIVE ULTRASOUND IN DETECTION OF HEPATIC METASTASES
Authors: GORDON BA FLANAGAN FL DEHDASHTI F
Citation: Ba. Gordon et al., COMPARISON OF FDG-PET AND INTRAOPERATIVE ULTRASOUND IN DETECTION OF HEPATIC METASTASES, The Journal of nuclear medicine, 38(5), 1997, pp. 513-513
PET ASSESSMENT OF OUTCOME IN CHILDHOOD EPILEPSY
Authors: GORDON BA DEHDASHTI F
Citation: Ba. Gordon et F. Dehdashti, PET ASSESSMENT OF OUTCOME IN CHILDHOOD EPILEPSY, Radiology, 205, 1997, pp. 1655-1655
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
A 66-BASEPAIR INSERTION IN EXON-6 OF THE ALPHA-L-FUCOSIDASE GENE OF AFUCOSIDOSIS PATIENT
Authors: SEO HC YANG MH KIM AH OBRIEN JS DICIOCCIO RA GORDON BA
Citation: Hc. Seo et al., A 66-BASEPAIR INSERTION IN EXON-6 OF THE ALPHA-L-FUCOSIDASE GENE OF AFUCOSIDOSIS PATIENT, Human mutation, 7(2), 1996, pp. 183-183
HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA (HHH)-SYNDROME - ULTRASTRUCTURAL-CHANGES OF MITOCHONDRIA IN CULTURED DERMAL FIBROBLASTS OF 3 PATIENTS
Authors: HAUST MD DEWAR RA GATFIELD DP GORDON BA
Citation: Md. Haust et al., HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA (HHH)-SYNDROME - ULTRASTRUCTURAL-CHANGES OF MITOCHONDRIA IN CULTURED DERMAL FIBROBLASTS OF 3 PATIENTS, Pathology research and practice, 192(3), 1996, pp. 271-280
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
FUCOSIDOSIS WITH DYSTONIA
Authors: GORDON BA GORDON KE SEO HC YANG M DICIOCCIO RA OBRIEN JS
Citation: Ba. Gordon et al., FUCOSIDOSIS WITH DYSTONIA, Neuropediatrics, 26(6), 1995, pp. 325-327
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
PYOMYOSITIS - CHARACTERISTICS AT CT AND MR-IMAGING
Authors: GORDON BA MARTINEZ S COLLINS AJ
Citation: Ba. Gordon et al., PYOMYOSITIS - CHARACTERISTICS AT CT AND MR-IMAGING, Radiology, 197(1), 1995, pp. 279-286
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
ATAXIA IN INSTITUTIONALIZED PATIENTS WITH EPILEPSY
Authors: YOUNG GB OPPENHEIMER SR GORDON BA WELLS GA ASSIS LPA KREEFT JH LOHUIS NA BLUME WT
Citation: Gb. Young et al., ATAXIA IN INSTITUTIONALIZED PATIENTS WITH EPILEPSY, Canadian journal of neurological sciences, 21(3), 1994, pp. 252-258
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
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