Gisela Nogales-Gadea School for Mental Health and Neuroscience Maastricht University Biography Publications Institution JoVE Articles Gisela Nogales-Gadea has not added a biography. If you are Gisela Nogales-Gadea and would like to personalize this page please email our Author Liaison for assistance. Publications McArdle Disease: Update of Reported Mutations and Polymorphisms in the PYGM Gene Human Mutation. Apr, 2015 | Pubmed ID: 25914343 The Pathogenomics of McArdle Disease--genes, Enzymes, Models, and Therapeutic Implications Journal of Inherited Metabolic Disease. Mar, 2015 | Pubmed ID: 25053163 McArdle Disease Does Not Affect Skeletal Muscle Fibre Type Profiles in Humans Biology Open. 2014 | Pubmed ID: 25432515 Clinical and Scientific Aspects of Acetylcholine Receptor Myasthenia Gravis Current Opinion in Neurology. Oct, 2014 | Pubmed ID: 25105461 McArdle Disease: a Unique Study Model in Sports Medicine Sports Medicine (Auckland, N.Z.). Nov, 2014 | Pubmed ID: 25028051 Proteasome Inhibition with Bortezomib Depletes Plasma Cells and Specific Autoantibody Production in Primary Thymic Cell Cultures from Early-onset Myasthenia Gravis Patients Journal of Immunology (Baltimore, Md. : 1950). Aug, 2014 | Pubmed ID: 24973445 Analysis of Serum MiRNA Profiles of Myasthenia Gravis Patients PloS One. 2014 | Pubmed ID: 24637658 Altered RIG-I/DDX58-mediated Innate Immunity in Dermatomyositis The Journal of Pathology. Jul, 2014 | Pubmed ID: 24604766 Neurofascin IgG4 Antibodies in CIDP Associate with Disabling Tremor and Poor Response to IVIg Neurology. Mar, 2014 | Pubmed ID: 24523485 Specific Contactin N-glycans Are Implicated in Neurofascin Binding and Autoimmune Targeting in Peripheral Neuropathies The Journal of Biological Chemistry. Mar, 2014 | Pubmed ID: 24497634 Clinical and Molecular Characterization of Mcardle's Disease in Brazilian Patients Neuromolecular Medicine. May, 2013 | Pubmed ID: 23653251 Antibodies to Contactin-1 in Chronic Inflammatory Demyelinating Polyneuropathy Annals of Neurology. Mar, 2013 | Pubmed ID: 23280477 Knock-in Mice for the R50X Mutation in the PYGM Gene Present with McArdle Disease Brain : a Journal of Neurology. Jul, 2012 | Pubmed ID: 22730558 A Transcriptomic Approach to Search for Novel Phenotypic Regulators in McArdle Disease PloS One. 2012 | Pubmed ID: 22347505 Genotypic and Phenotypic Features of McArdle Disease: Insights from the Spanish National Registry Journal of Neurology, Neurosurgery, and Psychiatry. Mar, 2012 | Pubmed ID: 22250184 Are Mitochondrial Haplogroups Associated with Extreme Longevity? A Study on a Spanish Cohort Age (Dordrecht, Netherlands). Feb, 2012 | Pubmed ID: 21274636 Are Mitochondrial Haplogroups Associated with Elite Athletic Status? A Study on a Spanish Cohort Mitochondrion. Nov, 2011 | Pubmed ID: 21856449 Expression of Glycogen Phosphorylase Isoforms in Cultured Muscle from Patients with McArdle's Disease Carrying the P.R771PfsX33 PYGM Mutation PloS One. 2010 | Pubmed ID: 20957198 Excessive Skeletal Muscle Recruitment During Strenuous Exercise in McArdle Patients European Journal of Applied Physiology. Nov, 2010 | Pubmed ID: 20683610 The Second Wind Phenomenon in Very Young McArdle's Patients Neuromuscular Disorders : NMD. Jun, 2009 | Pubmed ID: 19477644 McArdle Disease: What Do Neurologists Need to Know? Nature Clinical Practice. Neurology. Oct, 2008 | Pubmed ID: 18833216 Expression of the Muscle Glycogen Phosphorylase Gene in Patients with McArdle Disease: the Role of Nonsense-mediated MRNA Decay Human Mutation. Feb, 2008 | Pubmed ID: 17994553 Favorable Responses to Acute and Chronic Exercise in McArdle Patients Clinical Journal of Sport Medicine : Official Journal of the Canadian Academy of Sport Medicine. Jul, 2007 | Pubmed ID: 17620784 The 577X Allele of the ACTN3 Gene is Associated with Improved Exercise Capacity in Women with McArdle's Disease Neuromuscular Disorders : NMD. Aug, 2007 | Pubmed ID: 17560787 A Proposed Molecular Diagnostic Flowchart for Myophosphorylase Deficiency (McArdle Disease) in Blood Samples from Spanish Patients Human Mutation. Feb, 2007 | Pubmed ID: 17221871 A Novel Exon 5 Mutation (N139H) in the SOD1 Gene in a Spanish Family Associated with Incomplete Penetrance Journal of the Neurological Sciences. Apr, 2004 | Pubmed ID: 15050430 अमर छाँटे बी कोशिकाओं से पुनः संयोजक मानव आईजीजी मोनोक्लोनल एंटीबॉडी का सृजन Gisela Nogales-Gadea*1,2, Abhishek Saxena*1, Carolin Hoffmann*1, Judith Hounjet1, Daniëlle Coenen1, Peter Molenaar1, Mario Losen1, Pilar Martinez-Martinez1 1School for Mental Health and Neuroscience, Maastricht University, 2Department of Neurosciences, Institut d'Investigació Germans Trias i Pujol Immunology and Infection
अमर छाँटे बी कोशिकाओं से पुनः संयोजक मानव आईजीजी मोनोक्लोनल एंटीबॉडी का सृजन Gisela Nogales-Gadea*1,2, Abhishek Saxena*1, Carolin Hoffmann*1, Judith Hounjet1, Daniëlle Coenen1, Peter Molenaar1, Mario Losen1, Pilar Martinez-Martinez1 1School for Mental Health and Neuroscience, Maastricht University, 2Department of Neurosciences, Institut d'Investigació Germans Trias i Pujol Immunology and Infection
