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Journal of the Neurological Sciences, ISSN 0022-510X, 08/2019, Volume 403, pp. 114 - 116
Journal Article
Journal of Neuroinflammation, ISSN 1742-2094, 09/2016, Volume 13, Issue 1, pp. 280 - 280
Background: A subset of patients with neuromyelitis optica spectrum disorders (NMOSD) has been shown to be seropositive for myelin oligodendrocyte glycoprotein... 
Aquaporin-4 antibodies (AQP4-IgG, NMO-IgG) | Therapy | Multiple sclerosis | Natalizumab | Optic neuritis | Vaccination | Electrophysiology | Infections | Longitudinally extensive transverse myelitis | Cerebrospinal fluid | Ofatumumab | Transverse myelitis | McDonald criteria | International consensus diagnostic criteria for neuromyelitis optica spectrum disorders | Evoked potentials | Methotrexate | Glatiramer acetate | Autoantibodies | Rituximab | Oligoclonal bands | Pregnancy | Treatment | Magnetic resonance imaging | Myelin oligodendrocyte glycoprotein antibodies (MOG-IgG) | Outcome | Interferon beta | Wingerchuk criteria 2006 and 2015 | IPND criteria | Neuromyelitis optica spectrum disorders (NMOSD) | Azathioprine | Barkhof criteria | Methotrexate Azathioprine | MEDUSA-HEAD ATAXIA | ANTIDIURETIC-HORMONE SECRETION | IMMUNOLOGY | MULTIPLE-SCLEROSIS | MYELIN-OLIGODENDROCYTE GLYCOPROTEIN | EXTENSIVE TRANSVERSE MYELITIS | PURKINJE-CELL ANTIBODIES | SPINAL-CORD BIOPSY | POSITIVE NEUROMYELITIS-OPTICA | PREGNANCY-RELATED RELAPSE | NEUROSCIENCES | OPTICA SPECTRUM DISORDER | Myelin-Oligodendrocyte Glycoprotein - immunology | Myelin-Oligodendrocyte Glycoprotein - genetics | Brain - diagnostic imaging | Age Distribution | Neuromyelitis Optica - therapy | Humans | Middle Aged | Cardiolipins - immunology | Male | Young Adult | Vaccination - methods | Neuromyelitis Optica - cerebrospinal fluid | HEK293 Cells | Anti-Inflammatory Agents - therapeutic use | Adult | Female | Child | Optic Nerve - diagnostic imaging | Aquaporin 4 - immunology | Treatment Outcome | Neuromyelitis Optica - diagnostic imaging | Autoantibodies - cerebrospinal fluid | Adolescent | Sex Factors | Aged | Neuromyelitis Optica - epidemiology | Cohort Studies | Vision Disorders - etiology | Measurement | Care and treatment | Physiological aspects | Development and progression | Neuromyelitis optica | Diagnosis | Research | Index Medicus
Journal Article
NeuroImage, ISSN 1053-8119, 12/2018, Volume 183, pp. 150 - 172
Journal Article
Journal of Neuro-Oncology, ISSN 0167-594X, 1/2017, Volume 131, Issue 2, pp. 267 - 276
Journal Article
Journal Article
Brain, ISSN 0006-8950, 11/2015, Volume 138, Issue 11, pp. 3316 - 3326
The spinocerebellar ataxias types 2 (SCA2) and 3 (SCA3) are autosomal dominantly inherited cerebellar ataxias which are caused by CAG trinucleotide repeat... 
substantia nigra | parkinsonism | spinocerebellar ataxias | subthalamic nucleus | PET | SPINOCEREBELLAR ATAXIA TYPE-2 | RESPONSIVE PARKINSONISM | DOMINANT CEREBELLAR ATAXIAS | CONFIRMATION | PARCELLATION | CLINICAL-FEATURES | NEUROSCIENCES | CLINICAL NEUROLOGY | MACHADO-JOSEPH-DISEASE | DEEP BRAIN-STIMULATION | Dopamine Plasma Membrane Transport Proteins - metabolism | Substantia Nigra - pathology | Dopaminergic Neurons - pathology | Parkinsonian Disorders - complications | Humans | Middle Aged | Machado-Joseph Disease - diagnostic imaging | Male | Positron-Emission Tomography | Substantia Nigra - metabolism | Case-Control Studies | Ataxin-2 - genetics | Young Adult | Dopaminergic Neurons - diagnostic imaging | Machado-Joseph Disease - complications | Dopaminergic Neurons - metabolism | Parkinsonian Disorders - diagnostic imaging | Aged, 80 and over | Adult | Female | Neostriatum - metabolism | Machado-Joseph Disease - pathology | Spinocerebellar Ataxias - genetics | Neostriatum - pathology | Spinocerebellar Ataxias - complications | Parkinson Disease - diagnostic imaging | Spinocerebellar Ataxias - diagnostic imaging | Repressor Proteins - genetics | Spinocerebellar Ataxias - pathology | Trinucleotide Repeat Expansion | Substantia Nigra - diagnostic imaging | Aged | Neostriatum - diagnostic imaging | Ataxin-3 - genetics | Machado-Joseph Disease - genetics | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article
Human Brain Mapping, ISSN 1065-9471, 08/2017, Volume 38, Issue 8, pp. 4157 - 4168
IntroductionFriedreich's ataxia (FRDA) is the most common autosomal-recessive ataxia worldwide. It is characterized by early onset, sensory abnormalities, and... 
Friedreich's ataxia | MRI | LOFA | multiatlas approach | cortical thickness |