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Thomas Voit

Showing results (21-30 of 160) with videos related to

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Journal of Human Genetics|February 19, 2016
Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegiaLena Willkomm, Raul Heredia, Katrin Hoffmann, et al.
Neuromuscular Disorders : NMD|October 6, 2009
Gait analysis using accelerometry in dystrophin-deficient dogsInès Barthélémy, Eric Barrey, Jean-Laurent Thibaud, et al.
Journal of Virology|August 2, 2013
C-reactive protein (CRP) is essential for efficient systemic transduction of recombinant adeno-associated virus vector 1 (rAAV-1) and rAAV-6 in miceJerome Denard, Beatrice Marolleau, Christine Jenny, et al.
Muscle & Nerve|December 5, 2006
Tandem duplication of DMD exon 18 associated with epilepsy, macroglossia, and endocrinologic abnormalitiesClaudia Weiss, Sibylle Jakubiczka, Angela Huebner, et al.
Metabolites|May 24, 2024
Effect of Fluid Intake on Acute Changes in Plasma Volume: A Randomized Controlled Crossover Pilot TrialJanis Schierbauer, Sabrina Sanfilippo, Auguste Grothoff, et al.
NMR in Biomedicine|July 29, 2015
Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophyClaire Wary, Noura Azzabou, Céline Giraudeau, et al.
Journal of Neuromuscular Diseases|October 5, 2018
Home-Based Monitoring of Pulmonary Function in Patients with Duchenne Muscular DystrophGunnar M Buyse, Christian Rummey, Thomas Meier, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Defective protein glycosylation in patients with cutis laxa syndromeEva Morava, Suzan Wopereis, Paul Coucke, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 12, 2013
AAV genome loss from dystrophic mouse muscles during AAV-U7 snRNA-mediated exon-skipping therapyMaëva Le Hir, Aurélie Goyenvalle, Cécile Peccate, et al.
Brain & Development|May 3, 2005
Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in JapanYasushi Ito, Elena Gertsen, Hirokazu Oguni, et al.
Pageof 16

Showing results (21-30 of 160) with videos related to

Sort By:
Pageof 16
Journal of Human Genetics|February 19, 2016
Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegiaLena Willkomm, Raul Heredia, Katrin Hoffmann, et al.
Neuromuscular Disorders : NMD|October 6, 2009
Gait analysis using accelerometry in dystrophin-deficient dogsInès Barthélémy, Eric Barrey, Jean-Laurent Thibaud, et al.
Journal of Virology|August 2, 2013
C-reactive protein (CRP) is essential for efficient systemic transduction of recombinant adeno-associated virus vector 1 (rAAV-1) and rAAV-6 in miceJerome Denard, Beatrice Marolleau, Christine Jenny, et al.
Muscle & Nerve|December 5, 2006
Tandem duplication of DMD exon 18 associated with epilepsy, macroglossia, and endocrinologic abnormalitiesClaudia Weiss, Sibylle Jakubiczka, Angela Huebner, et al.
Metabolites|May 24, 2024
Effect of Fluid Intake on Acute Changes in Plasma Volume: A Randomized Controlled Crossover Pilot TrialJanis Schierbauer, Sabrina Sanfilippo, Auguste Grothoff, et al.
NMR in Biomedicine|July 29, 2015
Quantitative NMRI and NMRS identify augmented disease progression after loss of ambulation in forearms of boys with Duchenne muscular dystrophyClaire Wary, Noura Azzabou, Céline Giraudeau, et al.
Journal of Neuromuscular Diseases|October 5, 2018
Home-Based Monitoring of Pulmonary Function in Patients with Duchenne Muscular DystrophGunnar M Buyse, Christian Rummey, Thomas Meier, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Defective protein glycosylation in patients with cutis laxa syndromeEva Morava, Suzan Wopereis, Paul Coucke, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 12, 2013
AAV genome loss from dystrophic mouse muscles during AAV-U7 snRNA-mediated exon-skipping therapyMaëva Le Hir, Aurélie Goyenvalle, Cécile Peccate, et al.
Brain & Development|May 3, 2005
Clinical presentation, EEG studies, and novel mutations in two cases of GLUT1 deficiency syndrome in JapanYasushi Ito, Elena Gertsen, Hirokazu Oguni, et al.
Pageof 16