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Angela Abicht

Showing results (21-30 of 102) with videos related to

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Neuromuscular Disorders : NMD|December 23, 2021
Cutaneous T-cell lymphoma mimicking myopathy with lipoatrophyMiriam Hiebeler, Markus Reinholz, Michael Flaig, et al.
Seminars in Pediatric Neurology|July 3, 2018
The Curse of Apneic SpellsJosefine Radke, Mona Dreesmann, Michael Radke, et al.
Human Mutation|February 13, 2020
Critical assessment of secondary findings in genes linked to primary arrhythmia syndromesIsabel Diebold, Ulrike Schön, Florentine Scharf, et al.
Journal of the Peripheral Nervous System : JPNS|February 21, 2020
Genotype-phenotype correlation in a novel ABHD12 mutation underlying PHARC syndromeAndreas Thimm, Ahmad Rahal, Ulrike Schoen, et al.
Neuropediatrics|December 27, 2016
Stroke as Initial Manifestation of Adenosine Deaminase 2 DeficiencyMiriam Elbracht, Michael Mull, Norbert Wagner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 11, 2019
Characteristic clinical and ultrastructural findings in nesprinopathiesHeike Kölbel, Angela Abicht, Oliver Schwartz, et al.
Frontiers in Neuroscience|February 4, 2026
Novel <i>NPRL3</i> variant associated with sleep-related hypermotor epilepsy: a case report and educational reviewSerena Broggi, Kai-Nicolas Poppert, Matthias Mauritz, et al.
Neuromuscular Disorders : NMD|March 11, 2017
Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiencyBertold Schrank, Benedikt Schoser, Thomas Klopstock, et al.
Muscle & Nerve|March 26, 2016
Novel genetic and neuropathological insights in neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP)Kristl G Claeys, Angela Abicht, Martin Häusler, et al.
Neuromuscular Disorders : NMD|October 16, 2004
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndromeJuliane S Müller, Angela Abicht, Hans-Jürgen Christen, et al.
Pageof 11

Showing results (21-30 of 102) with videos related to

Sort By:
Pageof 11
Neuromuscular Disorders : NMD|December 23, 2021
Cutaneous T-cell lymphoma mimicking myopathy with lipoatrophyMiriam Hiebeler, Markus Reinholz, Michael Flaig, et al.
Seminars in Pediatric Neurology|July 3, 2018
The Curse of Apneic SpellsJosefine Radke, Mona Dreesmann, Michael Radke, et al.
Human Mutation|February 13, 2020
Critical assessment of secondary findings in genes linked to primary arrhythmia syndromesIsabel Diebold, Ulrike Schön, Florentine Scharf, et al.
Journal of the Peripheral Nervous System : JPNS|February 21, 2020
Genotype-phenotype correlation in a novel ABHD12 mutation underlying PHARC syndromeAndreas Thimm, Ahmad Rahal, Ulrike Schoen, et al.
Neuropediatrics|December 27, 2016
Stroke as Initial Manifestation of Adenosine Deaminase 2 DeficiencyMiriam Elbracht, Michael Mull, Norbert Wagner, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 11, 2019
Characteristic clinical and ultrastructural findings in nesprinopathiesHeike Kölbel, Angela Abicht, Oliver Schwartz, et al.
Frontiers in Neuroscience|February 4, 2026
Novel <i>NPRL3</i> variant associated with sleep-related hypermotor epilepsy: a case report and educational reviewSerena Broggi, Kai-Nicolas Poppert, Matthias Mauritz, et al.
Neuromuscular Disorders : NMD|March 11, 2017
Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiencyBertold Schrank, Benedikt Schoser, Thomas Klopstock, et al.
Muscle & Nerve|March 26, 2016
Novel genetic and neuropathological insights in neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP)Kristl G Claeys, Angela Abicht, Martin Häusler, et al.
Neuromuscular Disorders : NMD|October 16, 2004
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndromeJuliane S Müller, Angela Abicht, Hans-Jürgen Christen, et al.
Pageof 11