M M Ling|B H Robinson - JoVE Visualize

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Journal of Child Neurology|April 1, 1991

Infant-onset progressive myoclonus epilepsyM G Harbord, P A Hwang, B H Robinson, et al.

Pathology|May 19, 2001

Gastrointestinal colonisation of vancomycin-resistant enterococcus in a Singapore teaching hospitalL L Oon, M M Ling, Y F Chiew

Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association|January 1, 1977

Comparison of whole body and regional assessments of calcium balance in renal osteodystrophy in the response to 1 alpha-hydroxy vitamin D3R B Naik, P W Robertson, B H Robinson, et al.

Human Mutation|March 25, 1999

Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunctionS Raha, F Merante, E Shoubridge, et al.

Journal of Neurogenetics|April 1, 1984

3-Hydroxy-3-methylglutaric aciduriaC L Greene, H M Cann, B H Robinson, et al.

American Journal of Human Genetics|March 1, 1995

Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complexK Chun, N MacKay, R Petrova-Benedict, et al.

Neuropediatrics|May 28, 2008

Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxiaF-G Debray, M Lambert, R Gagne, et al.

Genomics|November 1, 1993

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13S T Ali, A M Duncan, K Schappert, et al.

Biochimica Et Biophysica Acta|April 16, 1998

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mtDNA depletion syndromeM F Marusich, B H Robinson, J W Taanman, et al.

British Medical Journal|September 20, 1975

Agonal phase, ischaemic times, and renal vascular abnormalities and outcome of cadaver kidney transplantsC L Hall, J R Sansom, M Obeid, et al.

Pageof 21

Showing results (161-170 of 202) with videos related to

Sort By:

Pageof 21

Journal of Child Neurology|April 1, 1991

Infant-onset progressive myoclonus epilepsyM G Harbord, P A Hwang, B H Robinson, et al.

Pathology|May 19, 2001

Gastrointestinal colonisation of vancomycin-resistant enterococcus in a Singapore teaching hospitalL L Oon, M M Ling, Y F Chiew

Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association|January 1, 1977

Comparison of whole body and regional assessments of calcium balance in renal osteodystrophy in the response to 1 alpha-hydroxy vitamin D3R B Naik, P W Robertson, B H Robinson, et al.

Human Mutation|March 25, 1999

Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunctionS Raha, F Merante, E Shoubridge, et al.

Journal of Neurogenetics|April 1, 1984

3-Hydroxy-3-methylglutaric aciduriaC L Greene, H M Cann, B H Robinson, et al.

American Journal of Human Genetics|March 1, 1995

Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complexK Chun, N MacKay, R Petrova-Benedict, et al.

Neuropediatrics|May 28, 2008

Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxiaF-G Debray, M Lambert, R Gagne, et al.

Genomics|November 1, 1993

Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13S T Ali, A M Duncan, K Schappert, et al.

Biochimica Et Biophysica Acta|April 16, 1998

Expression of mtDNA and nDNA encoded respiratory chain proteins in chemically and genetically-derived Rho0 human fibroblasts: a comparison of subunit proteins in normal fibroblasts treated with ethidium bromide and fibroblasts from a patient with mtDNA depletion syndromeM F Marusich, B H Robinson, J W Taanman, et al.

British Medical Journal|September 20, 1975

Agonal phase, ischaemic times, and renal vascular abnormalities and outcome of cadaver kidney transplantsC L Hall, J R Sansom, M Obeid, et al.

Pageof 21