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Christopher Lindberg

Showing results (31-40 of 56) with videos related to

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Neuromuscular Disorders : NMD|February 2, 2015
Mitochondrial pathology in inclusion body myositisUlrika Lindgren, Sara Roos, Carola Hedberg Oldfors, et al.
Neuropathology and Applied Neurobiology|August 18, 2021
Proteomic characterisation of polyglucosan bodies in skeletal muscle in RBCK1 deficiencyChrister Thomsen, Edoardo Malfatti, Ana Jovanovic, et al.
Acta Neurologica Scandinavica|September 2, 2020
Progressive external ophthalmoplegia associated with novel MT-TN mutationsKittichate Visuttijai, Carola Hedberg-Oldfors, Ulrika Lindgren, et al.
Frontiers in Immunology|November 9, 2017
A Sensitive Method for Detecting Peptide-specific CD4<sup>+</sup> T Cell Responses in Peripheral Blood from Patients with Myasthenia GravisSapna Sharma, Clas Malmeström, Christopher Lindberg, et al.
American Journal of Medical Genetics. Part A|September 3, 2013
Timing of diagnosis of patients with Pompe disease: data from the Pompe registryPriya S Kishnani, Hernán M Amartino, Christopher Lindberg, et al.
Molecular Genetics and Metabolism|August 3, 2014
Methods of diagnosis of patients with Pompe disease: Data from the Pompe RegistryPriya S Kishnani, Hernán M Amartino, Christopher Lindberg, et al.
Acta Neuropathologica|November 25, 2024
Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiencyCarola Hedberg-Oldfors, Ulrika Lindgren, Kittichate Visuttijai, et al.
Neuromuscular Disorders : NMD|December 24, 2013
Late-onset spinal motor neuronopathy - a common form of dominant SMASini Penttilä, Manu Jokela, Sanna Huovinen, et al.
European Journal of Human Genetics : EJHG|February 11, 2005
Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutationsGittan Kollberg, Monica Jansson, Asa Pérez-Bercoff, et al.
Brain Pathology (Zurich, Switzerland)|December 23, 2020
Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencingCarola Hedberg-Oldfors, Ulrika Lindgren, Swaraj Basu, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Neuromuscular Disorders : NMD|February 2, 2015
Mitochondrial pathology in inclusion body myositisUlrika Lindgren, Sara Roos, Carola Hedberg Oldfors, et al.
Neuropathology and Applied Neurobiology|August 18, 2021
Proteomic characterisation of polyglucosan bodies in skeletal muscle in RBCK1 deficiencyChrister Thomsen, Edoardo Malfatti, Ana Jovanovic, et al.
Acta Neurologica Scandinavica|September 2, 2020
Progressive external ophthalmoplegia associated with novel MT-TN mutationsKittichate Visuttijai, Carola Hedberg-Oldfors, Ulrika Lindgren, et al.
Frontiers in Immunology|November 9, 2017
A Sensitive Method for Detecting Peptide-specific CD4<sup>+</sup> T Cell Responses in Peripheral Blood from Patients with Myasthenia GravisSapna Sharma, Clas Malmeström, Christopher Lindberg, et al.
American Journal of Medical Genetics. Part A|September 3, 2013
Timing of diagnosis of patients with Pompe disease: data from the Pompe registryPriya S Kishnani, Hernán M Amartino, Christopher Lindberg, et al.
Molecular Genetics and Metabolism|August 3, 2014
Methods of diagnosis of patients with Pompe disease: Data from the Pompe RegistryPriya S Kishnani, Hernán M Amartino, Christopher Lindberg, et al.
Acta Neuropathologica|November 25, 2024
Lipid storage myopathy associated with sertraline treatment is an acquired mitochondrial disorder with respiratory chain deficiencyCarola Hedberg-Oldfors, Ulrika Lindgren, Kittichate Visuttijai, et al.
Neuromuscular Disorders : NMD|December 24, 2013
Late-onset spinal motor neuronopathy - a common form of dominant SMASini Penttilä, Manu Jokela, Sanna Huovinen, et al.
European Journal of Human Genetics : EJHG|February 11, 2005
Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutationsGittan Kollberg, Monica Jansson, Asa Pérez-Bercoff, et al.
Brain Pathology (Zurich, Switzerland)|December 23, 2020
Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencingCarola Hedberg-Oldfors, Ulrika Lindgren, Swaraj Basu, et al.
Pageof 6