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R E Bittner

Showing results (1-10 of 31) with videos related to

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Neuromuscular Disorders : NMD|January 5, 2000
Cardiac involvement in Becker's muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvementJ Finsterer, R E Bittner, M Grimm
British Journal of Anaesthesia|July 1, 1997
Dystrophin deficient mdx muscle is not prone to MH susceptibility: an in vitro studyN Mader, H Gilly, R E Bittner
Lancet (London, England)|May 3, 1997
Angina for 14 yearsC Stöllberger, J Finsterer, R E Bittner
Clinical Neuropathology|February 13, 1999
Cerebrospinal fluid filtration and immunoglobulins in multifocal motor neuropathyJ Finsterer, B Schwerer, R E Bittner, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[Lactate determination at rest and during bicycle ergometry in healthy probands and in patients with mitochondrial myopathies]S Shorny, J Finsterer, R E Bittner, et al.
Heart (British Cardiac Society)|October 1, 1996
Left ventricular non-compaction in a patient with becker's muscular dystrophyC Stöllberger, J Finsterer, G Blazek, et al.
Neurology|January 5, 2002
CPEO associated with a single nucleotide deletion in the mitochondrial tRNA(Tyr) geneT Raffelsberger, W Rossmanith, H Thaller-Antlanger, et al.
The Journal of Cell Biology|December 1, 1992
Direct visualization of the dystrophin network on skeletal muscle fiber membraneV Straub, R E Bittner, J J Léger, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[In vitro transformation of amniotic cells to muscle cells--background and outlook]B Streubel, G Martucci-Ivessa, T Fleck, et al.
Anatomy and Embryology|February 1, 1997
Dystrophin expression in heterozygous mdx/+ mice indicates imprinting of X chromosome inactivation by parent-of-origin-, tissue-, strain- and position-dependent factorsR E Bittner, I Popoff, S Shorny, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|January 5, 2000
Cardiac involvement in Becker's muscular dystrophy, necessitating heart transplantation, 6 years before apparent skeletal muscle involvementJ Finsterer, R E Bittner, M Grimm
British Journal of Anaesthesia|July 1, 1997
Dystrophin deficient mdx muscle is not prone to MH susceptibility: an in vitro studyN Mader, H Gilly, R E Bittner
Lancet (London, England)|May 3, 1997
Angina for 14 yearsC Stöllberger, J Finsterer, R E Bittner
Clinical Neuropathology|February 13, 1999
Cerebrospinal fluid filtration and immunoglobulins in multifocal motor neuropathyJ Finsterer, B Schwerer, R E Bittner, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[Lactate determination at rest and during bicycle ergometry in healthy probands and in patients with mitochondrial myopathies]S Shorny, J Finsterer, R E Bittner, et al.
Heart (British Cardiac Society)|October 1, 1996
Left ventricular non-compaction in a patient with becker's muscular dystrophyC Stöllberger, J Finsterer, G Blazek, et al.
Neurology|January 5, 2002
CPEO associated with a single nucleotide deletion in the mitochondrial tRNA(Tyr) geneT Raffelsberger, W Rossmanith, H Thaller-Antlanger, et al.
The Journal of Cell Biology|December 1, 1992
Direct visualization of the dystrophin network on skeletal muscle fiber membraneV Straub, R E Bittner, J J Léger, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1996
[In vitro transformation of amniotic cells to muscle cells--background and outlook]B Streubel, G Martucci-Ivessa, T Fleck, et al.
Anatomy and Embryology|February 1, 1997
Dystrophin expression in heterozygous mdx/+ mice indicates imprinting of X chromosome inactivation by parent-of-origin-, tissue-, strain- and position-dependent factorsR E Bittner, I Popoff, S Shorny, et al.
Pageof 4