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Peter M Andersen

Showing results (151-160 of 241) with videos related to

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Nature Genetics|February 28, 2006
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisMatthew J Greenway, Peter M Andersen, Carsten Russ, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 30, 2023
Determining impairment in the Swedish, Polish and German ECAS: the importance of adjusting for age and educationJulia Finsel, Ivar Winroth, Katarzyna Ciećwierska, et al.
Annals of Neurology|July 3, 2003
Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosisAmmar Al-Chalabi, Margaret D Scheffler, Bradley N Smith, et al.
Brain : a Journal of Neurology|September 26, 2022
The impact of age on genetic testing decisions in amyotrophic lateral sclerosisPuja R Mehta, Alfredo Iacoangeli, Sarah Opie-Martin, et al.
Cells|July 6, 2023
Live Cell Imaging of ATP Levels Reveals Metabolic Compartmentalization within Motoneurons and Early Metabolic Changes in <i>FUS</i> ALS MotoneuronsVitaly L Zimyanin, Anna-Maria Pielka, Hannes Glaß, et al.
Genes|January 21, 2022
Heterozygous <i>DHTKD1</i> Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis PatientsAlma Osmanovic, Isabel Gogol, Helge Martens, et al.
European Journal of Neurology|September 15, 2011
EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)--revised report of an EFNS task force, Peter M Andersen, Sharon Abrahams, et al.
Scientific Reports|September 23, 2018
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral SclerosisBastien Paré, Manuela Lehmann, Marie Beaudin, et al.
Human Molecular Genetics|May 15, 2013
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosisJudith Eschbach, Birgit Schwalenstöcker, Selma M Soyal, et al.
Cellular and Molecular Life Sciences : CMLS|July 22, 2018
Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALSAnika M Helferich, Sarah J Brockmann, Jörg Reinders, et al.
Pageof 25

Showing results (151-160 of 241) with videos related to

Sort By:
Pageof 25
Nature Genetics|February 28, 2006
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisMatthew J Greenway, Peter M Andersen, Carsten Russ, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 30, 2023
Determining impairment in the Swedish, Polish and German ECAS: the importance of adjusting for age and educationJulia Finsel, Ivar Winroth, Katarzyna Ciećwierska, et al.
Annals of Neurology|July 3, 2003
Ciliary neurotrophic factor genotype does not influence clinical phenotype in amyotrophic lateral sclerosisAmmar Al-Chalabi, Margaret D Scheffler, Bradley N Smith, et al.
Brain : a Journal of Neurology|September 26, 2022
The impact of age on genetic testing decisions in amyotrophic lateral sclerosisPuja R Mehta, Alfredo Iacoangeli, Sarah Opie-Martin, et al.
Cells|July 6, 2023
Live Cell Imaging of ATP Levels Reveals Metabolic Compartmentalization within Motoneurons and Early Metabolic Changes in <i>FUS</i> ALS MotoneuronsVitaly L Zimyanin, Anna-Maria Pielka, Hannes Glaß, et al.
Genes|January 21, 2022
Heterozygous <i>DHTKD1</i> Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis PatientsAlma Osmanovic, Isabel Gogol, Helge Martens, et al.
European Journal of Neurology|September 15, 2011
EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)--revised report of an EFNS task force, Peter M Andersen, Sharon Abrahams, et al.
Scientific Reports|September 23, 2018
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral SclerosisBastien Paré, Manuela Lehmann, Marie Beaudin, et al.
Human Molecular Genetics|May 15, 2013
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosisJudith Eschbach, Birgit Schwalenstöcker, Selma M Soyal, et al.
Cellular and Molecular Life Sciences : CMLS|July 22, 2018
Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALSAnika M Helferich, Sarah J Brockmann, Jörg Reinders, et al.
Pageof 25