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R E Bittner

Showing results (21-30 of 31) with videos related to

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Journal of the Neurological Sciences|September 19, 1998
Lactate stress test in the diagnosis of mitochondrial myopathyJ Finsterer, S Shorny, J Capek, et al.
The Journal of Cell Biology|December 21, 2000
MAP1B is required for axon guidance and Is involved in the development of the central and peripheral nervous systemA Meixner, S Haverkamp, H Wässle, et al.
Neuromuscular Disorders : NMD|March 1, 1995
Sarcolemmal expression of dystrophin C-terminus but reduced expression of 6q-dystrophin-related protein in two DMD patients with large deletions of the dystrophin geneR E Bittner, S Shorny, R Ferlings, et al.
Neuropediatrics|August 30, 2002
Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathyN Barisic, G Bernert, O Ipsiroglu, et al.
Anatomy and Embryology|April 30, 1999
Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx miceR E Bittner, C Schöfer, K Weipoltshammer, et al.
Neurology|October 26, 2005
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP geneD Haubenberger, R E Bittner, S Rauch-Shorny, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathyIngrid Bader, M Freilinger, F Landauer, et al.
Neuroreport|March 10, 2001
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutationE Vafiadaki, A Reis, S Keers, et al.
Neuropediatrics|May 28, 2008
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndromeM Auer-Grumbach, C Fischer, L Papić, et al.
Nature Genetics|October 3, 1999
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2BR E Bittner, L V Anderson, E Burkhardt, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Journal of the Neurological Sciences|September 19, 1998
Lactate stress test in the diagnosis of mitochondrial myopathyJ Finsterer, S Shorny, J Capek, et al.
The Journal of Cell Biology|December 21, 2000
MAP1B is required for axon guidance and Is involved in the development of the central and peripheral nervous systemA Meixner, S Haverkamp, H Wässle, et al.
Neuromuscular Disorders : NMD|March 1, 1995
Sarcolemmal expression of dystrophin C-terminus but reduced expression of 6q-dystrophin-related protein in two DMD patients with large deletions of the dystrophin geneR E Bittner, S Shorny, R Ferlings, et al.
Neuropediatrics|August 30, 2002
Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathyN Barisic, G Bernert, O Ipsiroglu, et al.
Anatomy and Embryology|April 30, 1999
Recruitment of bone-marrow-derived cells by skeletal and cardiac muscle in adult dystrophic mdx miceR E Bittner, C Schöfer, K Weipoltshammer, et al.
Neurology|October 26, 2005
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP geneD Haubenberger, R E Bittner, S Rauch-Shorny, et al.
Orphanet Journal of Rare Diseases|July 19, 2022
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathyIngrid Bader, M Freilinger, F Landauer, et al.
Neuroreport|March 10, 2001
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutationE Vafiadaki, A Reis, S Keers, et al.
Neuropediatrics|May 28, 2008
Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndromeM Auer-Grumbach, C Fischer, L Papić, et al.
Nature Genetics|October 3, 1999
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2BR E Bittner, L V Anderson, E Burkhardt, et al.
Pageof 4