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H F Busch

Showing results (31-40 of 63) with videos related to

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Molecular and Cellular Biochemistry|October 6, 1997
Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compoundsH R Scholte, Y Yu, J D Ross, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1986
Myopathy with abnormal mitochondria, transient low electron transport capacity in the respiratory chain, and absence of energy transduction at sites 1 and 2 in vitroU Trockel, H R Scholte, K V Toyka, et al.
Brain : a Journal of Neurology|September 1, 1980
Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic studyC J Höweler, H F Busch, L F Bernini, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 9, 1993
[Application of combined DNA and dystrophin protein analysis in the diagnosis of Duchenne's and Becker's muscular dystrophy in 102 Dutch patients]H B Ginjaar, E Bakker, H F Busch, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Riboflavin-responsive complex I deficiencyH R Scholte, H F Busch, H D Bakker, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 25, 1993
[Intravenously-administered immunoglobulins as first-choice agent in juvenile dermatomyositis]D A Breems, P W de Haas, F Visscher, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cellsH R Scholte, H F Busch, I E Luyt-Houwen, et al.
Lancet (London, England)|July 25, 1992
Prenatal diagnosis of myotonic dystrophy by direct mutation analysisH J Smeets, W M Nillesen, F Los, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosisH D Bakker, H R Scholte, J A Jeneson, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 6, 1993
[Intravenously administered immunoglobulin first-choice remedy in autoimmune diseases?]D A Breems, P W de Haas, F Visscher, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
Molecular and Cellular Biochemistry|October 6, 1997
Rapid isolation of muscle and heart mitochondria, the lability of oxidative phosphorylation and attempts to stabilize the process in vitro by taurine, carnitine and other compoundsH R Scholte, Y Yu, J D Ross, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1986
Myopathy with abnormal mitochondria, transient low electron transport capacity in the respiratory chain, and absence of energy transduction at sites 1 and 2 in vitroU Trockel, H R Scholte, K V Toyka, et al.
Brain : a Journal of Neurology|September 1, 1980
Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic studyC J Höweler, H F Busch, L F Bernini, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 9, 1993
[Application of combined DNA and dystrophin protein analysis in the diagnosis of Duchenne's and Becker's muscular dystrophy in 102 Dutch patients]H B Ginjaar, E Bakker, H F Busch, et al.
Biochimica Et Biophysica Acta|May 24, 1995
Riboflavin-responsive complex I deficiencyH R Scholte, H F Busch, H D Bakker, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 25, 1993
[Intravenously-administered immunoglobulins as first-choice agent in juvenile dermatomyositis]D A Breems, P W de Haas, F Visscher, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cellsH R Scholte, H F Busch, I E Luyt-Houwen, et al.
Lancet (London, England)|July 25, 1992
Prenatal diagnosis of myotonic dystrophy by direct mutation analysisH J Smeets, W M Nillesen, F Los, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Vitamin-responsive complex I deficiency in a myopathic patient with increased activity of the terminal respiratory chain and lactic acidosisH D Bakker, H R Scholte, J A Jeneson, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 6, 1993
[Intravenously administered immunoglobulin first-choice remedy in autoimmune diseases?]D A Breems, P W de Haas, F Visscher, et al.
Pageof 7