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Angela Abicht

Showing results (1-10 of 102) with videos related to

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Neuropediatrics|August 23, 2012
Congenital myasthenic syndromes: current diagnostic and therapeutic approachesUlrike Schara, Adela Della Marina, Angela Abicht
BMJ Case Reports|December 11, 2012
Exercise-induced myalgia and rhabdomyolysis in a patient with the rare m.3243A>T mtDNA mutationDavid Czell, Angela Abicht, Jürgen Hench, et al.
Clinical Neurology and Neurosurgery|August 26, 2020
Dilative cardiomyopathy displaying double trouble etiology: Myocarditis and Mcleod syndrome?Federica Montagnese, Ulrich Grabmaier, Angela Abicht, et al.
Neuromuscular Disorders : NMD|August 14, 2012
DOK7 limb-girdle myasthenic syndrome mimicking congenital muscular dystrophyIbrahim Mahjneh, Hanns Lochmüller, Francesco Muntoni, et al.
Expert Reviews in Molecular Medicine|August 10, 2007
Congenital myasthenic syndromes: spotlight on genetic defects of neuromuscular transmissionJuliane S Müller, Violeta Mihaylova, Angela Abicht, et al.
Journal of Neuromuscular Diseases|March 8, 2021
Effect of Discontinuation of Nusinersen Treatment in Long-Standing SMA3Miriam Hiebeler, Angela Abicht, Peter Reilich, et al.
Practical Neurology|July 30, 2022
Persistent hypokalaemia and intermittent muscle weaknessMonika Rabenstein, Angela Abicht, Anna Brunn, et al.
European Journal of Pediatrics|January 25, 2012
Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutationFlorian Brackmann, Angela Abicht, Uwe Ahting, et al.
Cardiovascular Diagnosis and Therapy|May 10, 2021
Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counselingAngela Abicht, Ulrike Schön, Andreas Laner, et al.
Neuropediatrics|October 21, 2020
Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 VariantsMatthias Eckenweiler, Johannes A Mayr, Sarah Grünert, et al.
Pageof 11

Showing results (1-10 of 102) with videos related to

Sort By:
Pageof 11
Neuropediatrics|August 23, 2012
Congenital myasthenic syndromes: current diagnostic and therapeutic approachesUlrike Schara, Adela Della Marina, Angela Abicht
BMJ Case Reports|December 11, 2012
Exercise-induced myalgia and rhabdomyolysis in a patient with the rare m.3243A>T mtDNA mutationDavid Czell, Angela Abicht, Jürgen Hench, et al.
Clinical Neurology and Neurosurgery|August 26, 2020
Dilative cardiomyopathy displaying double trouble etiology: Myocarditis and Mcleod syndrome?Federica Montagnese, Ulrich Grabmaier, Angela Abicht, et al.
Neuromuscular Disorders : NMD|August 14, 2012
DOK7 limb-girdle myasthenic syndrome mimicking congenital muscular dystrophyIbrahim Mahjneh, Hanns Lochmüller, Francesco Muntoni, et al.
Expert Reviews in Molecular Medicine|August 10, 2007
Congenital myasthenic syndromes: spotlight on genetic defects of neuromuscular transmissionJuliane S Müller, Violeta Mihaylova, Angela Abicht, et al.
Journal of Neuromuscular Diseases|March 8, 2021
Effect of Discontinuation of Nusinersen Treatment in Long-Standing SMA3Miriam Hiebeler, Angela Abicht, Peter Reilich, et al.
Practical Neurology|July 30, 2022
Persistent hypokalaemia and intermittent muscle weaknessMonika Rabenstein, Angela Abicht, Anna Brunn, et al.
European Journal of Pediatrics|January 25, 2012
Classical MERRF phenotype associated with mitochondrial tRNA(Leu) (m.3243A>G) mutationFlorian Brackmann, Angela Abicht, Uwe Ahting, et al.
Cardiovascular Diagnosis and Therapy|May 10, 2021
Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counselingAngela Abicht, Ulrike Schön, Andreas Laner, et al.
Neuropediatrics|October 21, 2020
Thiamine Treatment and Favorable Outcome in an Infant with Biallelic TPK1 VariantsMatthias Eckenweiler, Johannes A Mayr, Sarah Grünert, et al.
Pageof 11