The New England Journal of Medicine, ISSN 0028-4793, 01/2017, Volume 376, Issue 3, pp. 209 - 220
Patients with primary progressive MS who received the anti-CD20+ humanized antibody ocrelizumab were less likely to have clinical deterioration that was...
CD20 | MULTICENTER TRIAL | DEMYELINATION | DOUBLE-BLIND | CANCER-RISK | ANTIBODY | PATHOLOGY | DAMAGE | MEDICINE, GENERAL & INTERNAL | Antibodies, Monoclonal, Humanized - adverse effects | Brain - diagnostic imaging | Antibodies, Monoclonal, Humanized - therapeutic use | Antigens, CD20 | Double-Blind Method | Multiple Sclerosis, Chronic Progressive - immunology | T-Lymphocytes | Humans | Middle Aged | Male | Disease Progression | Young Adult | Magnetic Resonance Imaging | B-Lymphocytes - immunology | Adolescent | Infusions, Intravenous - adverse effects | Intention to Treat Analysis | Lymphocyte Count | Adult | Female | Multiple Sclerosis, Chronic Progressive - drug therapy | Neuroimaging | Multiple sclerosis | Intravenous administration | Pathogenesis | Clinical trials | Patients | Placebo effect | Magnetic resonance imaging | Lymphocytes B | Lymphocytes | Immunotherapy | Immunopathogenesis | Monoclonal antibodies | CD20 antigen | Respiratory tract diseases | Life Sciences | Human health and pathology
CD20 | MULTICENTER TRIAL | DEMYELINATION | DOUBLE-BLIND | CANCER-RISK | ANTIBODY | PATHOLOGY | DAMAGE | MEDICINE, GENERAL & INTERNAL | Antibodies, Monoclonal, Humanized - adverse effects | Brain - diagnostic imaging | Antibodies, Monoclonal, Humanized - therapeutic use | Antigens, CD20 | Double-Blind Method | Multiple Sclerosis, Chronic Progressive - immunology | T-Lymphocytes | Humans | Middle Aged | Male | Disease Progression | Young Adult | Magnetic Resonance Imaging | B-Lymphocytes - immunology | Adolescent | Infusions, Intravenous - adverse effects | Intention to Treat Analysis | Lymphocyte Count | Adult | Female | Multiple Sclerosis, Chronic Progressive - drug therapy | Neuroimaging | Multiple sclerosis | Intravenous administration | Pathogenesis | Clinical trials | Patients | Placebo effect | Magnetic resonance imaging | Lymphocytes B | Lymphocytes | Immunotherapy | Immunopathogenesis | Monoclonal antibodies | CD20 antigen | Respiratory tract diseases | Life Sciences | Human health and pathology
Journal Article
Acta Neurologica Scandinavica, ISSN 0001-6314, 08/2011, Volume 124, Issue 2, pp. 75 - 84
Gold R, Wolinsky JS. Pathophysiology of multiple sclerosis and the place of teriflunomide.
Acta Neurol Scand: 2011: 124: 75–84.
© 2010 John Wiley & Sons A/S....
teriflunomide | immunomodulator | immunology | multiple sclerosis | relapsing/remitting | disease‐modifying therapies | Immunomodulator | Teriflunomide | Multiple sclerosis | Immunology | Relapsing/remitting | Disease-modifying therapies | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | SUSCEPTIBILITY | NATURAL-HISTORY | CLINICAL NEUROLOGY | PATHOGENESIS | disease-modifying therapies | MEDICAL PROGRESS | GENETICS | DISEASE | ANIMAL-MODELS | LEFLUNOMIDE | T-CELLS | Toluidines - therapeutic use | Anti-Inflammatory Agents - pharmacology | Humans | Crotonates - pharmacology | Toluidines - pharmacology | Clinical Trials as Topic | Multiple Sclerosis - classification | Multiple Sclerosis - physiopathology | Crotonates - therapeutic use | Models, Immunological | Animals | Anti-Inflammatory Agents - therapeutic use | Multiple Sclerosis - pathology | Pyrimidines | Biological response modifiers | T cells | Interferon beta | Gold | Animal models | Antiinflammatory agents | Preservation | Myelin | Central nervous system | Clinical trials | Inflammation | Lymphocytes T | Macrophages | beta -Interferon | Lymphocytes B | Magnetic resonance imaging | copolymer 1 | Oligodendrocytes | pyrimidines
teriflunomide | immunomodulator | immunology | multiple sclerosis | relapsing/remitting | disease‐modifying therapies | Immunomodulator | Teriflunomide | Multiple sclerosis | Immunology | Relapsing/remitting | Disease-modifying therapies | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | SUSCEPTIBILITY | NATURAL-HISTORY | CLINICAL NEUROLOGY | PATHOGENESIS | disease-modifying therapies | MEDICAL PROGRESS | GENETICS | DISEASE | ANIMAL-MODELS | LEFLUNOMIDE | T-CELLS | Toluidines - therapeutic use | Anti-Inflammatory Agents - pharmacology | Humans | Crotonates - pharmacology | Toluidines - pharmacology | Clinical Trials as Topic | Multiple Sclerosis - classification | Multiple Sclerosis - physiopathology | Crotonates - therapeutic use | Models, Immunological | Animals | Anti-Inflammatory Agents - therapeutic use | Multiple Sclerosis - pathology | Pyrimidines | Biological response modifiers | T cells | Interferon beta | Gold | Animal models | Antiinflammatory agents | Preservation | Myelin | Central nervous system | Clinical trials | Inflammation | Lymphocytes T | Macrophages | beta -Interferon | Lymphocytes B | Magnetic resonance imaging | copolymer 1 | Oligodendrocytes | pyrimidines
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2017, Volume 376, Issue 3, pp. 221 - 234
In two trials involving patients with relapsing multiple sclerosis, the anti-CD20+ monoclonal antibody ocrelizumab was associated with lower annualized relapse...
TRIAL | MEDICINE, GENERAL & INTERNAL | ANTIBODIES TARGETING CD20 | DEMYELINATION | RITUXIMAB | B-CELL DEPLETION | DISEASE | CANCER-RISK | DISABILITY | PATHOLOGY | PROSPECTS | Antibodies, Monoclonal, Humanized - adverse effects | Recurrence | Brain - diagnostic imaging | Antibodies, Monoclonal, Humanized - therapeutic use | Antigens, CD20 | Multiple Sclerosis, Relapsing-Remitting - drug therapy | Humans | Middle Aged | Male | Disease Progression | Interferon-beta - therapeutic use | Magnetic Resonance Imaging | B-Lymphocytes - immunology | Interferon-beta - adverse effects | Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging | Infusions, Intravenous - adverse effects | Adult | Female | Immunologic Factors - adverse effects | Immunologic Factors - therapeutic use | Multiple sclerosis | Intravenous administration | Lymphocytes B | Lymphocytes | β-Interferon | Immunotherapy | Clinical trials | Monoclonal antibodies | CD20 antigen | Gadolinium | Cognition | Interferon
TRIAL | MEDICINE, GENERAL & INTERNAL | ANTIBODIES TARGETING CD20 | DEMYELINATION | RITUXIMAB | B-CELL DEPLETION | DISEASE | CANCER-RISK | DISABILITY | PATHOLOGY | PROSPECTS | Antibodies, Monoclonal, Humanized - adverse effects | Recurrence | Brain - diagnostic imaging | Antibodies, Monoclonal, Humanized - therapeutic use | Antigens, CD20 | Multiple Sclerosis, Relapsing-Remitting - drug therapy | Humans | Middle Aged | Male | Disease Progression | Interferon-beta - therapeutic use | Magnetic Resonance Imaging | B-Lymphocytes - immunology | Interferon-beta - adverse effects | Multiple Sclerosis, Relapsing-Remitting - diagnostic imaging | Infusions, Intravenous - adverse effects | Adult | Female | Immunologic Factors - adverse effects | Immunologic Factors - therapeutic use | Multiple sclerosis | Intravenous administration | Lymphocytes B | Lymphocytes | β-Interferon | Immunotherapy | Clinical trials | Monoclonal antibodies | CD20 antigen | Gadolinium | Cognition | Interferon
Journal Article
Annals of Neurology, ISSN 0364-5134, 2011, Volume 69, Issue 2, pp. 292 - 302
New evidence and consensus has led to further revision of the McDonald Criteria for diagnosis of multiple sclerosis. The use of imaging for demonstration of...
RADIOLOGICALLY ISOLATED SYNDROME | SPINAL-CORD LESIONS | INTRACORTICAL LESIONS | DIFFERENTIAL-DIAGNOSIS | INVERSION-RECOVERY | NEUROMYELITIS-OPTICA | GENERAL NEUROLOGY PRACTICE | HIGH-FIELD MRI | CLINICALLY ISOLATED SYNDROMES | CORTICAL-LESIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | Magnetic Resonance Imaging | Multiple Sclerosis - diagnosis | Early Diagnosis | Humans | Sensitivity and Specificity | Revisions | Multiple sclerosis | Older people | Rapid Communication | Neurologi | Clinical Medicine | Neurology | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
RADIOLOGICALLY ISOLATED SYNDROME | SPINAL-CORD LESIONS | INTRACORTICAL LESIONS | DIFFERENTIAL-DIAGNOSIS | INVERSION-RECOVERY | NEUROMYELITIS-OPTICA | GENERAL NEUROLOGY PRACTICE | HIGH-FIELD MRI | CLINICALLY ISOLATED SYNDROMES | CORTICAL-LESIONS | NEUROSCIENCES | CLINICAL NEUROLOGY | Magnetic Resonance Imaging | Multiple Sclerosis - diagnosis | Early Diagnosis | Humans | Sensitivity and Specificity | Revisions | Multiple sclerosis | Older people | Rapid Communication | Neurologi | Clinical Medicine | Neurology | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Neurology, ISSN 0028-3878, 2014, Volume 83, Issue 3, pp. 278 - 286
Accurate clinical course descriptions (phenotypes) of multiple sclerosis (MS) are important for communication, prognostication, design and recruitment of...
PATHOGENESIS | RADIOLOGICALLY ISOLATED SYNDROME | DIAGNOSIS | CONVERSION | DISEASE | SPINAL-CORD | FOLLOW-UP | NATURAL-HISTORY | BRAIN MRI | CLINICAL NEUROLOGY | Multiple Sclerosis - physiopathology | Humans | Clinical Trials as Topic - standards | Societies, Medical - standards | Multiple Sclerosis - therapy | Consensus | Multiple Sclerosis - classification | Views & Reviews
PATHOGENESIS | RADIOLOGICALLY ISOLATED SYNDROME | DIAGNOSIS | CONVERSION | DISEASE | SPINAL-CORD | FOLLOW-UP | NATURAL-HISTORY | BRAIN MRI | CLINICAL NEUROLOGY | Multiple Sclerosis - physiopathology | Humans | Clinical Trials as Topic - standards | Societies, Medical - standards | Multiple Sclerosis - therapy | Consensus | Multiple Sclerosis - classification | Views & Reviews
Journal Article
Lancet Neurology, ISSN 1474-4422, 2014, Volume 13, Issue 3, pp. 247 - 256
Summary Background Teriflunomide is an oral disease-modifying therapy approved for treatment of relapsing or relapsing–remitting multiple sclerosis. We aimed...
Neurology | BG-12 | OUTCOMES | EFFICACY | SAFETY | III TRIAL | CLINICAL NEUROLOGY | Double-Blind Method | Administration, Oral | Multiple Sclerosis, Relapsing-Remitting - drug therapy | Humans | Middle Aged | Male | Treatment Outcome | Multiple Sclerosis, Relapsing-Remitting - diagnosis | Toluidines - administration & dosage | Multiple Sclerosis, Relapsing-Remitting - epidemiology | Adult | Female | Crotonates - administration & dosage | Clinical trials | Medical colleges | Multiple sclerosis | Care and treatment | Voice recognition | Patient safety | Disease | Drug therapy | Drug dosages
Neurology | BG-12 | OUTCOMES | EFFICACY | SAFETY | III TRIAL | CLINICAL NEUROLOGY | Double-Blind Method | Administration, Oral | Multiple Sclerosis, Relapsing-Remitting - drug therapy | Humans | Middle Aged | Male | Treatment Outcome | Multiple Sclerosis, Relapsing-Remitting - diagnosis | Toluidines - administration & dosage | Multiple Sclerosis, Relapsing-Remitting - epidemiology | Adult | Female | Crotonates - administration & dosage | Clinical trials | Medical colleges | Multiple sclerosis | Care and treatment | Voice recognition | Patient safety | Disease | Drug therapy | Drug dosages
Journal Article
Lancet Neurology, ISSN 1474-4422, 2012, Volume 11, Issue 5, pp. 467 - 476
Summary Many of the available disability outcome measures used in clinical trials of multiple sclerosis are insensitive to change over time, inadequately...
Neurology | COGNITIVE DYSFUNCTION | FUNCTIONAL COMPOSITE | SECONDARY PROGRESSIVE MS | NATALIZUMAB | RELIABILITY | IMPACT SCALE MSIS-29 | QUALITY-OF-LIFE | VALIDITY | CLINICAL NEUROLOGY | DISEASE-ACTIVITY | IMPAIRMENT | Disability Evaluation | Retina - drug effects | Multiple Sclerosis - diagnosis | Tomography, Optical Coherence | Humans | Disease Progression | Randomized Controlled Trials as Topic | Brain - drug effects | Magnetic Resonance Imaging | Activities of Daily Living - classification | Neurologic Examination | Biomarkers | Brain - pathology | Retina - pathology | Multiple Sclerosis - drug therapy | Measurement | Clinical trials | Multiple sclerosis | Data processing | biomarkers | Quality of life
Neurology | COGNITIVE DYSFUNCTION | FUNCTIONAL COMPOSITE | SECONDARY PROGRESSIVE MS | NATALIZUMAB | RELIABILITY | IMPACT SCALE MSIS-29 | QUALITY-OF-LIFE | VALIDITY | CLINICAL NEUROLOGY | DISEASE-ACTIVITY | IMPAIRMENT | Disability Evaluation | Retina - drug effects | Multiple Sclerosis - diagnosis | Tomography, Optical Coherence | Humans | Disease Progression | Randomized Controlled Trials as Topic | Brain - drug effects | Magnetic Resonance Imaging | Activities of Daily Living - classification | Neurologic Examination | Biomarkers | Brain - pathology | Retina - pathology | Multiple Sclerosis - drug therapy | Measurement | Clinical trials | Multiple sclerosis | Data processing | biomarkers | Quality of life
Journal Article