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M Elleder

Showing results (161-170 of 191) with videos related to

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Casopis Lekaru Ceskych|March 23, 1990
[Fabry's disease with isolated disease of the cardiac muscle, manifesting as hypertrophic cardiomyopathy]M Elleder, V Dorazilová, V Bradová, et al.
Journal of Lipid Research|January 11, 2000
Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage diseaseP Lohse, S Maas, P Lohse, et al.
Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Cardiac manifestations in Fabry diseaseA Linhart, J C Lubanda, T Palecek, et al.
Vnitrni Lekarstvi|November 18, 2008
[The isolated form of cardiac amyloidosis in the form of beginning infiltrative cardiomyopathy without restrictive physiology]P Kuchynka, T Palecek, S Simek, et al.
Gene|February 28, 2012
Danon disease: a focus on processing of the novel LAMP2 mutation and comments on the beneficial use of peripheral white blood cells in the diagnosis of LAMP2 deficiencyF Majer, H Vlaskova, L Krol, et al.
Casopis Lekaru Ceskych|April 3, 2002
[Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome]M Capková, M Tesarová, L Wenchich, et al.
Casopis Lekaru Ceskych|September 28, 1998
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]L Stratilová, J Zeman, H Hansíková, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Lysosomal acid lipase deficiency. Overview of Czech patients]M Elleder, H Poupĕtová, J Ledvinová, et al.
Casopis Lekaru Ceskych|October 28, 1983
[Present trends and methodological basis for the cognitive process in pathology]P Mirejovský, B Bednár, M Elleder, et al.
Pageof 20

Showing results (161-170 of 191) with videos related to

Sort By:
Pageof 20
Casopis Lekaru Ceskych|March 23, 1990
[Fabry's disease with isolated disease of the cardiac muscle, manifesting as hypertrophic cardiomyopathy]M Elleder, V Dorazilová, V Bradová, et al.
Journal of Lipid Research|January 11, 2000
Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage diseaseP Lohse, S Maas, P Lohse, et al.
Neuropediatrics|August 26, 2004
Mitochondrial DNA depletion in Alpers syndromeM Tesarova, J A Mayr, L Wenchich, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Cardiac manifestations in Fabry diseaseA Linhart, J C Lubanda, T Palecek, et al.
Vnitrni Lekarstvi|November 18, 2008
[The isolated form of cardiac amyloidosis in the form of beginning infiltrative cardiomyopathy without restrictive physiology]P Kuchynka, T Palecek, S Simek, et al.
Gene|February 28, 2012
Danon disease: a focus on processing of the novel LAMP2 mutation and comments on the beneficial use of peripheral white blood cells in the diagnosis of LAMP2 deficiencyF Majer, H Vlaskova, L Krol, et al.
Casopis Lekaru Ceskych|April 3, 2002
[Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome]M Capková, M Tesarová, L Wenchich, et al.
Casopis Lekaru Ceskych|September 28, 1998
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]L Stratilová, J Zeman, H Hansíková, et al.
Casopis Lekaru Ceskych|April 4, 2000
[Lysosomal acid lipase deficiency. Overview of Czech patients]M Elleder, H Poupĕtová, J Ledvinová, et al.
Casopis Lekaru Ceskych|October 28, 1983
[Present trends and methodological basis for the cognitive process in pathology]P Mirejovský, B Bednár, M Elleder, et al.
Pageof 20