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134


Positron emission tomographic studies of aging and Alzheimer disease

de Leon MJ; Ferris SH; George AE; Christman DR; Fowler JS; Gentes C; Reisberg B; Gee B; Emmerich M; Yonekura Y; Brodie J; Kricheff II; Wolf AP
In this study the positron emission tomographic (PET)-18F-2-deoxy-2-fluoro-D-glucose (FDG) technique was used to study both normal aging and senile dementia. The results derived from 15 young normal subjects (mean age, 26 +/- 5 years) and 22 elderly normal subjects (mean age, 66 +/- 7 years) failed to indicate significant metabolic changes associated with age. A group of 24 patients with senile dementia (mean age, 73 +/- 7 years) showed consistent diminutions in regional glucose use relative to the elderly normals. Across all brain regions the diminutions were 17%-24%. There were also significant correlations between the measures of glucose use and the measures of cognitive functioning. Discriminant function classification analysis results indicate that better than 80% classification accuracy can be achieved for individual PET measures. These data suggest a possible future diagnostic use of PET in senile dementia.
PMID: 6410799
ISSN: 0195-6108
CID: 9486

Prevention of nitroprusside-induced cyanide toxicity with hydroxocobalamin

Cottrell JE; Casthely P; Brodie JD; Patel K; Klein A; Turndorf H
To investigate hydroxocobalamin's role in preventing cyanide intoxication from sodium nitroprusside, we studied two groups of patients. One group received nitroprusside alone, and the other received nitroprusside and hydroxocobalamin. Red-cell and plasma cyanide levels were 83.44 +/- 23.12 and 3.51 +/- 1.01 microgram per 100 ml after nitroprusside alone and were 33.18 +/- 17.29 and 2.18 +/- 0.65 microgram per 100 ml after nitroprusside plus hydroxocobalamin. Acidosis developed in patients with red-cell cyanide levels higher than 75 microgram per 100 ml. When hydroxocobalamin infusion was stopped before sodium nitroprusside infusion was discontinued, blood cyanide levels and base deficit increased in a manner similar to that in the untreated group. The dose of nitroprusside used in each group did not differ statistically. These data show that hydroxocobalamin prevents cyanide transfer from red cells and plasma to tissue after nitroprusside metabolism, and thereby prevents cyanide toxicity from large intravenous doses of the drug
PMID: 634316
ISSN: 0028-4793
CID: 45859

PREVENTION OF CYANIDE INTOXICATION FOLLOWING SODIUM NITROPRUSSIDE INDUCED HYPOTENSION [Meeting Abstract]

Cottrell, JE; Casthely, P; Brodie, JD; Patel, K; Klein, A; Turndorf, H
ISI:A1978ES73600050
ISSN: 0090-3493
CID: 29851

Mechanism and prevention of tachyphylaxis and cyanide toxicosis after nitroprusside-induced hypotension

Cottrell JE; Casthely P; Brodie JD; Patel K; Klein A; Turndorf H
PMID: 401173
ISSN: 0071-8041
CID: 11456

Margaret B : a "typical" Bellevue case

Brodie JD; Rohrs CC
ORIGINAL:0006686
ISSN: 0033-2712
CID: 105407

Subcellular distribution of methylmalonyl CoA carbonylmutase in human liver extracts

Morrow, G 3rd; Brodie, J D; Strimpler, A; Barness, L A
PMID: 4356662
ISSN: 0006-2944
CID: 156159

Cleavage of coenzyme B 12 by methylmalonyl coenzyme A mutase

Babior, B M; Woodams, A D; Brodie, J D
PMID: 4539956
ISSN: 0021-9258
CID: 132253

FAST AND SLOW INHIBITORS OF OX HEART SUCCINATE DEHYDROGENASE ACTION OF OXAL ACETATE AND ITS FLUORO ANALOGUES

KAPPEN L S; BRODIE J D; NICHOLLS P
BIOSIS:PREV197410045094
ISSN: 0300-5127
CID: 105406

Proton magnetic resonance of vitamin B 12 derivatives. Functioning of B 12 coenzymes

Brodie, J D; Poe, M
PMID: 4537738
ISSN: 0006-2960
CID: 156160

Mechanism of mammalian cobalamin-dependent methionine biosynthesis

Burke, G T; Mangum, J H; Brodie, J D
PMID: 5126926
ISSN: 0006-2960
CID: 132255