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1. Full Text CXCL13 is the major determinant for B cell recruitment to the CSF during neuroinflammation
by Kowarik, Markus C and Cepok, Sabine and Sellner, Johann and Grummel, Verena and Weber, Martin S and Korn, Thomas and Berthele, Achim and Hemmer, Bernhard
Journal of Neuroinflammation, ISSN 1742-2094, 05/2012, Volume 9, Issue 1, pp. 93 - 93
Background: The chemokines and cytokines CXCL13, CXCL12, CCL19, CCL21, BAFF and APRIL are believed to play a role in the recruitment of B cells to the central... 
B cells and plasmablasts | BAFF | CXCL12 | CCL21 | CCL19 | CXCL13 | APRIL | MULTIPLE-SCLEROSIS LESIONS | IMMUNOLOGY | CEREBROSPINAL-FLUID | ASTROCYTES | NEUROSCIENCES | LYME NEUROBORRELIOSIS | CENTRAL-NERVOUS-SYSTEM | LIGAND | CHEMOKINE CXCL13 | RECEPTORS | EXPRESSION | B-Lymphocyte Subsets - physiology | B-Lymphocyte Subsets - pathology | Humans | Middle Aged | Male | Nervous System Diseases - diagnosis | Cell Movement - physiology | Young Adult | Inflammation Mediators - cerebrospinal fluid | B-Lymphocyte Subsets - metabolism | Chemokine CXCL13 - biosynthesis | Adolescent | Inflammation Mediators - metabolism | Nervous System Diseases - cerebrospinal fluid | Adult | Female | Aged | Chemokine CXCL13 - cerebrospinal fluid | Cohort Studies | Nervous System Diseases - pathology | Nervous system diseases | Multiple sclerosis | Immune response | Cytokines | Immunoglobulin G | Albumin | Central nervous system diseases | B cells | Immunoglobulin A | Enzyme-linked immunosorbent assay | Chemokines | Flow cytometry | Disease | Manuscripts | Recruitment | Proteins | Studies | Lymphocytes | Herpes viruses | Ligands | Immune system
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2. Full Text Antibodies to native myelin oligodendrocyte glycoprotein in children with inflammatory demyelinating central nervous system disease
by Brilot, Fabienne and Dale, Russell C and Selter, Rebecca C and Grummel, Verena and Reddy Kalluri, Sudhakar and Aslam, Muhammad and Busch, Verena and Zhou, Dun and Cepok, Sabine and Hemmer, Bernhard
Annals of Neurology, ISSN 0364-5134, 12/2009, Volume 66, Issue 6, pp. 833 - 842
Objective Myelin oligodendrocyte glycoprotein (MOG) is a candidate target antigen in demyelinating diseases of the central nervous system (CNS). Although MOG... 
AUTOANTIBODIES | MULTIPLE-SCLEROSIS | AUTOIMMUNITY | ROLES | ACUTE DISSEMINATED ENCEPHALOMYELITIS | T-CELL | DIAGNOSTIC-CRITERIA | BASIC-PROTEIN | IDENTIFICATION | NEUROSCIENCES | ANTIMYELIN ANTIBODIES | CLINICAL NEUROLOGY | Central Nervous System - metabolism | Follow-Up Studies | Immunoglobulin G - blood | Humans | Central Nervous System - pathology | Child, Preschool | Myelin-Oligodendrocyte Glycoprotein | Infant | Male | Killer Cells, Natural - pathology | Encephalomyelitis, Acute Disseminated - blood | Central Nervous System - immunology | Nerve Tissue Proteins - metabolism | Myelin-Associated Glycoprotein - immunology | Encephalomyelitis, Acute Disseminated - immunology | Immunoglobulin G - cerebrospinal fluid | Myelin Proteins | Killer Cells, Natural - metabolism | Child
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3. Full Text Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
by Beecham, Ashley H and Patsopoulos, Nikolaos A and Xifara, Dionysia K and Davis, Mary F and Kemppinen, Anu and Cotsapas, Chris and Shah, Tejas S and Spencer, Chris and Booth, David and Goris, An and Oturai, Annette and Saarela, Janna and Fontaine, Bertrand and Hemmer, Bernhard and Martin, Claes and Zipp, Frauke and D'Alfonso, Sandra and Martinelli-Boneschi, Filippo and Taylor, Bruce and Harbo, Hanne F and Kockum, Ingrid and Hillert, Jan and Olsson, Tomas and Ban, Maria and Oksenberg, Jorge R and Hintzen, Rogier and Barcellos, Lisa F and Agliardi, Cristina and Alfredsson, Lars and Alizadeh, Mehdi and Anderson, Carl and Andrews, Robert and Søndergaard, Helle Bach and Baker, Amie and Band, Gavin and Baranzini, Sergio E and Barizzone, Nadia and Barrett, Jeffrey and Bellenguez, Céline and Bergamaschi, Laura and Bernardinelli, Luisa and Berthele, Achim and Biberacher, Viola and Binder, Thomas M.C and Blackburn, Hannah and Bomfim, Izaura L and Brambilla, Paola and Broadley, Simon and Brochet, Bruno and Brundin, Lou and Buck, Dorothea and Butzkueven, Helmut and Caillier, Stacy J and Camu, William and Carpentier, Wassila and Cavalla, Paola and Celius, Elisabeth G and Coman, Irène and Comi, Giancarlo and Corrado, Lucia and Cosemans, Leentje and Cournu-Rebeix, Isabelle and Cree, Bruce A.C and Cusi, Daniele and Damotte, Vincent and Defer, Gilles and Delgado, Silvia R and Deloukas, Panos and Di Sapio, Alessia and Dilthey, Alexander T and Donnelly, Peter and Dubois, Bénédicte and Duddy, Martin and Edkins, Sarah and Elovaara, Irina and Esposito, Federica and Evangelou, Nikos and Fiddes, Barnaby and Field, Judith and Franke, Andre and Freeman, Colin and Frohlich, Irene Y and Galimberti, Daniela and Gieger, Christian and Gourraud, Pierre-Antoine and Graetz, Christiane and Graham, Andrew and Grummel, Verena and Guaschino, Clara and Hadjixenofontos, Athena and Hakonarson, Hakon and Halfpenny, Christopher and Hall, Gillian and Hall, Per and Hamsten, Anders and Harley, James and Harrower, Timothy and Hawkins, Clive and Hellenthal, Garrett and Hillier, Charles and ... and Wellcome Trust Case Control Consor and Int IBD Genetics Consortium IIBDGC and International Multiple Sclerosis Genetics Consortium (IMSGC) and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International IBD Genetics Consortium (IIBDGC) and Institutionen för fysik, kemi och biologi and Linköpings universitet and Bioinformatik and Tekniska högskolan
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 11, pp. 1353 - 1362
Using the ImmunoChip custom genotyping array, we analyzed 14,498 subjects with multiple sclerosis and 24,091 healthy controls for 161,311 autosomal variants... 
AUTOIMMUNE | ALLELES | METAANALYSIS | GENOTYPE IMPUTATION | GENETIC RISK | INFORMATION | ANNOTATION | PRIMARY BILIARY-CIRRHOSIS | DISEASE | GENETICS & HEREDITY | GENOME-WIDE ASSOCIATION | Genetic Variation | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Gene Frequency | Humans | Multiple Sclerosis - immunology | Genotype | Multiple Sclerosis - genetics | Chromosome Mapping | Polymorphism, Single Nucleotide | Genetic Loci | Multiple sclerosis | Chromosome mapping | Genetic susceptibility | Genetic variation | Genetic aspects | Identification and classification | Methods | Testing | Confidence intervals | Disease | Quality control | Genomes | Stratigraphy | Autoimmune diseases | Gene expression | Meta-analysis | Teknik och teknologier | TEKNIKVETENSKAP | Engineering and Technology | TECHNOLOGY
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4. Full Text Clinical practice of analysis of anti-drug antibodies against interferon beta and natalizumab in multiple sclerosis patients in Europe: A descriptive study of test results
by Jenny, Link and Ryan, Ramanujam and Michael, Auer and Malin, Ryner and Signe, Hässler and Delphine, Bachelet and Cyprien, Mbogning and Clemens, Warnke and Dorothea, Buck and Poul, Erik Hyldgaard Jensen and Claudia, Sievers and Kathleen, Ingenhoven and Nicolas, Fissolo and Raija, Lindberg and Verena, Grummel and Naoimh, Donnellan and Manuel, Comabella and Xavier, Montalban and Bernd, Kieseier and Per, Soelberg Sørensen and Hans-Peter, Hartung and Tobias, Derfuss and Andy, Lawton and Dan, Sikkema and Marc, Pallardy and Bernhard, Hemmer and Florian, Deisenhammer and Philippe, Broët and Pierre, Dönnes and Julie, Davidson and Anna, Fogdell-Hahn and ABIRISK Consortium and Skolan för teknikvetenskap (SCI) and Matematik (Avd.) and Matematik (Inst.) and KTH
PLoS ONE, ISSN 1932-6203, 02/2017, Volume 12, Issue 2, p. e0170395
Antibodies against biopharmaceuticals (anti-drug antibodies, ADA) have been a well-integrated part of the clinical care of multiple sclerosis (MS) in several... 
REPORTER-GENE | IFN-BETA | MULTICENTER | NEUTRALIZING ANTIBODIES | THERAPY | ADALIMUMAB | MS-PATIENTS | MULTIDISCIPLINARY SCIENCES | VALIDATION | PREVALENCE | DISEASE PROGRESSION | Interferon-beta - immunology | Age Factors | Humans | Middle Aged | Natalizumab - adverse effects | Natalizumab - immunology | Child, Preschool | Infant | Male | Interferon-beta - therapeutic use | Young Adult | Time Factors | Interferon-beta - adverse effects | Natalizumab - therapeutic use | Aged, 80 and over | Antibodies - immunology | Adult | Female | Retrospective Studies | Child | Infant, Newborn | Europe | Immunologic Factors - immunology | Adolescent | Sex Factors | Multiple Sclerosis - immunology | Aged | Immunologic Factors - adverse effects | Immunologic Factors - therapeutic use | Multiple Sclerosis - drug therapy | Viral antibodies | Pharmaceutical research | Multiple sclerosis | Antibodies | Forecasts and trends | Drug discovery | Drug therapy | Testing | Drugs | Neurosciences | Data points | Immunoglobulins | Laboratories | Risk reduction | Medical screening | Patients | Biological activity | Consortia | Neurology | Hospitals | Immunogenicity | Rheumatoid arthritis | Interferon | Clinical medicine | Cost analysis | Monitoring | Mathematics | Naturvetenskap | Natural Sciences | Matematik
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5. Full Text Identification of a Pathogenic Antibody Response to Native Myelin Oligodendrocyte Glycoprotein in Multiple Sclerosis
by Dun Zhou and Rajneesh Srivastava and Stefan Nessler and Verena Grummel and Norbert Sommer and Wolfgang Brück and Hans-Peter Hartung and Christine Stadelmann and Bernhard Hemmer
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2006, Volume 103, Issue 50, pp. 19057 - 19062
Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system. Although the cause of MS is still uncertain, many findings point... 
Cytometry | Demyelinating diseases | Myelin | Humans | Cell lines | Antibodies | Oligodendroglia | Epitopes | Autoimmune diseases | Antibody formation | Axonal damage | Demyelination | Lentiviral expression | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | ALLERGIC ENCEPHALOMYELITIS | MULTIDISCIPLINARY SCIENCES | axonal damage | PERIPHERAL-BLOOD | CEREBROSPINAL-FLUID | ANTIMYELIN ANTIBODIES | demyelination | antibodies | CENTRAL-NERVOUS-SYSTEM | BASIC-PROTEIN | lentiviral expression | DEMYELINATING EVENT | LEWIS RAT | T-CELLS | Recombinant Proteins - metabolism | Autoantibodies - blood | Myelin-Associated Glycoprotein - genetics | Myelin-Associated Glycoprotein - metabolism | Myelin-Oligodendrocyte Glycoprotein | Rats | Multiple Sclerosis - genetics | Recombinant Proteins - genetics | Glioma - metabolism | Myelin Sheath - metabolism | Glioma - genetics | Autoantibodies - immunology | Myelin-Associated Glycoprotein - immunology | Animals | Multiple Sclerosis - immunology | Multiple Sclerosis - pathology | Myelin Proteins | Multiple Sclerosis - metabolism | Multiple sclerosis | Myelin proteins | Research | Biological Sciences
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6. Full Text Potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease
by Kraus, Verena and Srivastava, Rajneesh and Kalluri, Sudhakar Reddy and Seidel, Ulrich and Schuelke, Markus and Schimmel, Mareike and Rostasy, Kevin and Leiz, Steffen and Hosie, Stuart and Grummel, Verena and Hemmer, Bernhard
Neurology, ISSN 0028-3878, 02/2014, Volume 82, Issue 6, pp. 470 - 473
OBJECTIVE:A serum antibody against the inward rectifying potassium channel KIR4.1 (KIR4.1-IgG) was recently discovered, which is found in almost half of adult... 
PEDIATRIC MULTIPLE-SCLEROSIS | MOG | KIR4.1 | CLINICAL NEUROLOGY | Myelin-Oligodendrocyte Glycoprotein - immunology | Enzyme-Linked Immunosorbent Assay | Humans | Autoimmune Diseases - immunology | Child, Preschool | Infant | Male | Case-Control Studies | Autoantibodies - immunology | Immunoglobulin G - immunology | Potassium Channels, Inwardly Rectifying - immunology | Adolescent | Demyelinating Diseases - immunology | Nerve Fibers, Myelinated - immunology | Neuroglia - immunology | Multiple Sclerosis - immunology | Female | Brain - immunology | Child
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7. Full Text Cytokine and immune cell profiling in the cerebrospinal fluid of patients with neuro-inflammatory diseases
by Lepennetier, G and Hracsko, Z and Unger, M and Van Griensven, M and Grummel, V and Krumbholz, M and Berthele, A and Hemmer, B and Kowarik, MC
JOURNAL OF NEUROINFLAMMATION, ISSN 1742-2094, 11/2019, Volume 16, Issue 1, pp. 1 - 11
Background Cytokines play multiple roles during neuro-inflammatory processes and several cytokines have been studied in the context of specific diseases. This... 
Neuro-inflammation | NK cells | Cytokines | Immune cell subsets | CHEMOKINES | INTERLEUKIN-1-BETA | CNS | B cells | BACTERIAL | IMMUNOLOGY | CXCL13 | NEUROSCIENCES | Blood-brain barrier | MULTIPLE-SCLEROSIS | NEUROINFLAMMATION | CSF | PROGNOSTIC MARKER | CENTRAL-NERVOUS-SYSTEM | EXPRESSION
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8. Full Text Interferon-beta specific T cells are associated with the development of neutralizing antibodies in interferon-beta treated multiple sclerosis patients
by Kalluri, Sudhakar Reddy and Grummel, Verena and Hracsko, Zsuzsanna and Pongratz, Viola and Pernpeintner, Verena and Gasperi, Christiane and Buck, Dorothea and Hemmer, Bernhard and ABIRISK Consortium
Journal of Autoimmunity, ISSN 0896-8411, 03/2018, Volume 88, pp. 83 - 90
Beta-interferons are still among the most commonly used drugs to treat Multiple Sclerosis (MS). The use of beta-interferons is limited by the development of... 
Multiple sclerosis | Anti-drug antibodies | Neutralizing antibodies | Antigenic epitope | T cell | Interferon beta | THERAPEUTICS | TREATMENT REGIMEN | IMMUNOLOGY | IFN-BETA | IMMUNOGENICITY | IMPACT | THERAPY
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9. Full Text Natalizumab treatment decreases serum IgM and IgG levels in multiple sclerosis patients
by Selter, Rebecca C and Biberacher, Viola and Grummel, Verena and Buck, Dorothea and Eienbröker, Christian and Oertel, Wolfgang H and Berthele, Achim and Tackenberg, Björn and Hemmer, Bernhard
Multiple Sclerosis Journal, ISSN 1352-4585, 10/2013, Volume 19, Issue 11, pp. 1454 - 1461
Background: Treatment with natalizumab, a humanized monoclonal antibody against alpha4beta1 integrin, is associated with an increase in lymphoid progenitor... 
immunoglobulin G | Multiple sclerosis | immunoglobulin M | alpha4beta1 integrin | natalizumab | B cell homing | ALPHA-4-BETA-1 INTEGRIN | ACTIVATION | MARGINAL ZONE | VLA-4 | FLOW | CLINICAL NEUROLOGY | B-CELLS | ANTIBODY NATALIZUMAB | VCAM-1 | MEMORY | DIFFERENTIATION | Antibodies, Monoclonal, Humanized - adverse effects | Cross-Sectional Studies | Immunoglobulin G - blood | Multiple Sclerosis - blood | Natalizumab | Humans | Middle Aged | Male | B-Lymphocytes - drug effects | Immunoglobulin M - blood | Immunoglobulin A - blood | Adult | Female | Cohort Studies | Multiple Sclerosis - drug therapy
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10. Full Text Occurrence of anti-drug antibodies against interferon-beta and natalizumab in multiple sclerosis: A collaborative cohort analysis
by Bachelet, Delphine and Hässler, Signe and Mbogning, Cyprien and Link, Jenny and Ryner, Malin and Ramanujam, Ryan and Auer, Michael and Jensen, Poul Erik Hyldgaard and Koch-Henriksen, Nils and Warnke, Clemens and Ingenhoven, Kathleen and Buck, Dorothea and Grummel, Verena and Lawton, Andy and Donnellan, Naoimh and Hincelin-Mery, Agnès and Sikkema, Dan and Pallardy, Marc and Kieseier, Bernd and Hemmer, Bernard and Hartung, Hans Peter and Sorensen, Per Soelberg and Deisenhammer, Florian and Dönnes, Pierre and Davidson, Julie and Fogdell-Hahn, Anna and Broët, Philippe and ABIRISK Consortium and on behalf of the ABIRISK Consortium and Skolan för teknikvetenskap (SCI) and Matematik (Avd.) and Matematik (Inst.) and KTH
PLoS ONE, ISSN 1932-6203, 11/2016, Volume 11, Issue 11, p. e0162752
Immunogenicity of biopharmaceutical products in multiple sclerosis is a frequent side effect which has a multifactorial etiology. Here we study associations... 
IFN-BETA | VITAMIN-D | BINDING-ANTIBODIES | CONTROLLED-TRIAL | IMMUNOGENICITY | NEUTRALIZING ANTIBODIES | THERAPY | INTERVAL-CENSORED-DATA | AUTOIMMUNITY | MULTIDISCIPLINARY SCIENCES | T-CELLS | Interferon-beta - immunology | Humans | Middle Aged | Natalizumab - adverse effects | Natalizumab - immunology | Male | Multiple Sclerosis - epidemiology | Interferon-beta - therapeutic use | Interferon-beta - adverse effects | Natalizumab - therapeutic use | Antibodies - immunology | Adult | Female | Databases, Factual | Multiple Sclerosis - mortality | Antibodies, Anti-Idiotypic - blood | Risk Factors | Proportional Hazards Models | Antibodies, Anti-Idiotypic - immunology | Europe - epidemiology | Patient Outcome Assessment | Multiple Sclerosis - complications | Antibodies - blood | Aged | Population Surveillance | Cohort Studies | Multiple Sclerosis - drug therapy | Multiple sclerosis | Care and treatment | Development and progression | Interferon | Backup software | Biological response modifiers | Biopharmaceutics | Neurosciences | Immunoglobulins | Laboratories | β-Interferon | Antibodies | Systematic review | Regression analysis | Patients | Consortia | Neurology | Side effects | Demographics | Immunology | Vitamin D | Immunogenicity | Etiology | Collaboration | Biomarkers | Pharmaceuticals | Medical and Health Sciences | Medicin och hälsovetenskap
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11. Full Text Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis
by Buck, Dorothea and Albrecht, Eva and Aslam, Muhammad and Goris, An and Hauenstein, Natalie and Jochim, Angela and Cepok, Sabine and Grummel, Verena and Dubois, Bénédicte and Berthele, Achim and Lichtner, Peter and Gieger, Christian and Winkelmann, Juliane and Hemmer, Bernhard and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consortium and International Multiple Sclerosis Genetics Consortium and International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium
Annals of Neurology, ISSN 0364-5134, 01/2013, Volume 73, Issue 1, pp. 86 - 94
Objective: Intrathecal synthesis of immunoglobulin gamma (IgG) synthesis is frequently observed in patients with multiple sclerosis (MS). Whereas the extent of... 
OLIGOCLONAL BANDS | POPULATION | NEONATAL FC-RECEPTOR | RITUXIMAB | DISEASE | CSF | GM ALLOTYPES | ENVIRONMENTAL RISK-FACTORS | CEREBROSPINAL-FLUID | NEUROSCIENCES | BRAIN | CLINICAL NEUROLOGY | Multiple Sclerosis - diagnosis | Immunoglobulin gamma-Chains - genetics | Humans | Middle Aged | Genetic Loci - genetics | Immunoglobulin gamma-Chains - cerebrospinal fluid | Male | Multiple Sclerosis - genetics | Immunoglobulin Heavy Chains - cerebrospinal fluid | Young Adult | Immunoglobulin G - genetics | Immunoglobulin G - cerebrospinal fluid | Adolescent | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Genetic Variation - genetics | Biomarkers - cerebrospinal fluid | Genome-Wide Association Study - methods | Immunoglobulin Heavy Chains - genetics | Multiple Sclerosis - metabolism
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