B. H. Robinson - Concepedia

Author

B. H. Robinson

Also Known As

B H ROBINSON, B H Robinson, B H. Robinson, B. H. B. ROBINSON, B. H. B. Robinson, B. H. ROBINSON, B. H. Robinson, B.H Robinson, B.H. Robinson, B.H.B Robinson

258

Publications

7.9K

Citations

H-Index

169

Concepts

All Affiliations

University of Toronto Hospital for Sick Children SickKids Foundation University of Otago

About

B. H. Robinson is an author at University of Toronto specializing in medicine, biochemistry, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	47	3.3K
2	Engineering	16	25	625
3	Natural Sciences	15	19	961
4	Health Sciences	10	11	388
5	Public Health	1	1	233

B. H. Robinson

111

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. Y. Tatuch, John Christodoulou, Annette Feigenbaum, PubMed	1992	484
Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase. Sari Pitkänen, B. H. Robinson Journal of Clinical Investigation Superoxide Production RatesRedox SignalingNadh-coq ReductaseMitochondrial FunctionBiochemistry	1996	387
A bovine albumin peptide as a possible trigger of insulin-dependent diabetes mellitus Jukka Karjalainen, J. M. Martin, Mikael Knip, Journal of Endocrinological Investigation BiochemistryNatural SciencesMedicinePhysiologyDiabetes	1994	343
Nonviability of cells with oxidative defects in galactose medium: A screening test for affected patient fibroblasts B. H. Robinson, Roumyana Petrova-Benedict, J. Raymond Buncic, Biochemical Medicine and Metabolic Biology FibrosisScreening TestLipid PeroxidationExtracellular MatrixPathology	1992	271
Familial Hibernian Fever L. M. Williamson, D. Hull, Rohan Mehta, QJM Irish FamilyUnusual Periodic SyndromeSystemic DiseasesHigh EsrPathogenesis	1982	233
The inhibition of malate, tricarboxylate and oxoglutarate entry into mitochondria by 2-n-butylmalonate B. H. Robinson, Joseph Chappell Biochemical and Biophysical Research Communications Oxoglutarate EntryBiochemistryMitochondrial FunctionMedicineOrganelle Dynamic	1967	181
The Genetic Heterogeneity of Lactic Acidosis: Occurrence of Recognizable Inborn Errors of Metabolism in a Pediatric Population with Lactic Acidosis B. H. Robinson, Jennifer Taylor, W. G. Sherwood Pediatric Research Lactic AcidosisLactationInherited Metabolic DiseasePediatricsGenetic Heterogeneity	1980	168
Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy B. H. Robinson, Jennifer Taylor, W. G. Sherwood Pediatric Research Metabolic DiseasePhysiologyInherited Metabolic DiseasePediatricsDihydrolipoyl Dehydrogenase	1977	147
The Mitochondrial DNA Mutation at 8993 Associated with NARP Slows the Rate of ATP Synthesis in Isolated Lymphoblast Mitochondria Y. Tatuch, B. H. Robinson Biochemical and Biophysical Research Communications Genome InstabilityMitochondrial BiogenesisMitochondrial FunctionNatural SciencesGenetics	1993	142
Penetration of the mitochondrial membrane by glutamate and aspartate Arezki Azzi, Joseph Chappell, B. H. Robinson Biochemical and Biophysical Research Communications Mitochondrial FunctionBiochemistryMedicineMitochondrial MembraneMitochondrial Medicine	1967	132

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