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1. Full Text Movement Disorders in Treatable Inborn Errors of Metabolism
by Ebrahimi‐Fakhari, Darius and Van Karnebeek, Clara and Münchau, Alexander
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 598 - 613
inborn errors of metabolism | treatment | movement disorders | neurotransmitter disorders | neurogenetics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amino Acid Metabolism, Inborn Errors - complications | Niemann-Pick Disease, Type C - therapy | Hepatolenticular Degeneration - therapy | Monosaccharide Transport Proteins - deficiency | Amino Acid Metabolism, Inborn Errors - physiopathology | Humans | Folic Acid Deficiency - therapy | Hepatolenticular Degeneration - physiopathology | Vitamin E Deficiency - therapy | Dystonic Disorders - complications | Brain Diseases, Metabolic - diagnosis | Vitamin E Deficiency - diagnosis | Xanthomatosis, Cerebrotendinous - diagnosis | Basal Ganglia Diseases - diagnosis | Carbohydrate Metabolism, Inborn Errors - therapy | Dystonia - etiology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Parkinsonian Disorders - physiopathology | Chorea - physiopathology | Dystonia - physiopathology | Metabolic Diseases - diagnosis | Ataxia - diagnosis | Carbohydrate Metabolism, Inborn Errors - physiopathology | Metabolism, Inborn Errors - diagnosis | Folic Acid Deficiency - complications | Movement Disorders - physiopathology | Brain Diseases, Metabolic - physiopathology | Basal Ganglia Diseases - therapy | Ataxia - complications | Muscle Spasticity - physiopathology | Xanthomatosis, Cerebrotendinous - complications | Metabolic Diseases - complications | Metabolism, Inborn Errors - complications | Metabolism, Inborn Errors - physiopathology | Brain Diseases, Metabolic - complications | Glutaryl-CoA Dehydrogenase - deficiency | Carbohydrate Metabolism, Inborn Errors - complications | Ataxia - etiology | Hepatolenticular Degeneration - diagnosis | Metabolism, Inborn Errors - therapy | Niemann-Pick Disease, Type C - physiopathology | Parkinsonian Disorders - etiology | Amino Acid Metabolism, Inborn Errors - diagnosis | Brain Diseases, Metabolic - therapy | Xanthomatosis, Cerebrotendinous - therapy | Metabolic Diseases - therapy | Metabolic Diseases - physiopathology | Myoclonus - etiology | Vitamin E Deficiency - complications | Niemann-Pick Disease, Type C - diagnosis | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hepatolenticular Degeneration - complications | Vitamin E Deficiency - physiopathology | Ataxia - physiopathology | Ataxia - therapy | Chorea - etiology | Amino Acid Metabolism, Inborn Errors - therapy | Basal Ganglia Diseases - complications | Folic Acid Deficiency - physiopathology | Myoclonus - physiopathology | Muscle Spasticity - etiology | Dystonic Disorders - diagnosis | Basal Ganglia Diseases - physiopathology | Movement Disorders - etiology | Xanthomatosis, Cerebrotendinous - physiopathology | Folic Acid Deficiency - diagnosis | Niemann-Pick Disease, Type C - complications | Dystonic Disorders - etiology | Metabolism, Inborn errors of | Education | Mortality | Finance | Physiological aspects | Creatine | Movement disorders | Energy metabolism | Inborn errors of metabolism | Lysosomal storage diseases | Metabolism | Autophagy | Morbidity | Quality of life | Phenomenology | Psychiatrists | Differential diagnosis | Children | Phagocytosis | Index Medicus
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2. Full Text Neurological and Neuropsychiatric Impacts of COVID-19 Pandemic
by Roy, Devlina and Ghosh, Ritwik and Dubey, Souvik and Dubey, Mahua Jana and Benito-Leon, Julian and Kanti Ray, Biman
Canadian journal of neurological sciences, ISSN 0317-1671, 01/2021, Volume 48, Issue 1, pp. 9 - 24
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Meningoencephalitis - physiopathology | Parkinson Disease - therapy | Headache - etiology | Demyelinating Diseases - therapy | Humans | Cerebellar Ataxia - etiology | Ageusia - physiopathology | Meningoencephalitis - etiology | COVID-19 - psychology | Anosmia - etiology | Muscular Diseases - etiology | Ageusia - etiology | Cerebellar Ataxia - physiopathology | Nervous System Diseases - epidemiology | Seizures - physiopathology | SARS-CoV-2 | COVID-19 - complications | Muscular Diseases - physiopathology | Myelitis, Transverse - physiopathology | Myoclonus - etiology | Brain Diseases | Nervous System Diseases - physiopathology | Viral Tropism | COVID-19 - epidemiology | Stroke - therapy | Myelitis, Transverse - etiology | Cerebrovascular Disorders - physiopathology | Comorbidity | Alzheimer Disease - therapy | Guillain-Barre Syndrome - physiopathology | COVID-19 - physiopathology | Headache - physiopathology | Polyneuropathies - physiopathology | Cerebrovascular Disorders - etiology | Myoclonus - physiopathology | Hypoxia, Brain - physiopathology | Angiotensin-Converting Enzyme 2 | Dizziness - etiology | Dizziness - physiopathology | Polyneuropathies - etiology | Anosmia - physiopathology | Delivery of Health Care | Guillain-Barre Syndrome - etiology | Seizures - etiology | Nervous System Diseases - etiology | Disease Management | Epilepsy - therapy | Inflammation - physiopathology | Index Medicus
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3. Full Text The visual system in eyelid myoclonia with absences
by Vaudano, Anna Elisabetta and Ruggieri, Andrea and Tondelli, Manuela and Avanzini, Pietro and Benuzzi, Francesca and Gessaroli, Giuliana and Cantalupo, Gaetano and Mastrangelo, Massimo and Vignoli, Aglaia and Bonaventura, Carlo Di and Canevini, Maria Paola and Bernardina, Bernardo Dalla and Nichelli, Paolo Frigio and Meletti, Stefano
Annals of neurology, ISSN 0364-5134, 09/2014, Volume 76, Issue 3, pp. 412 - 427
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Prefrontal Cortex - physiopathology | Magnetic Resonance Imaging - methods | Male | Electroencephalography | Young Adult | Multimodal Imaging | Adult | Female | Cerebrum - physiopathology | Nerve Net - physiopathology | Visual Cortex - physiopathology | Epilepsies, Myoclonic - physiopathology | Epilepsies, Myoclonic - classification | Motor Cortex - physiopathology | Syndrome | Myoclonus - physiopathology | Epilepsy, Absence - physiopathology | Epilepsy, Reflex - physiopathology | Epilepsy, Generalized - physiopathology | Magnetic Resonance Imaging - instrumentation | Thalamus - physiopathology | Age of Onset | Brain Mapping | Ocular Motility Disorders - physiopathology | Brain | Medical research | Index Medicus
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4. Full Text Clinical and immunological characteristics of the spectrum of GFAP autoimmunity: a case series of 22 patients
by Iorio, Raffaele and Damato, Valentina and Evoli, Amelia and Gessi, Marco and Gaudino, Simona and Di Lazzaro, Vincenzo and Spagni, Gregorio and Sluijs, Jacqueline A and Hol, Elly M
Journal of neurology, neurosurgery and psychiatry, ISSN 0022-3050, 02/2018, Volume 89, Issue 2, pp. 138 - 146
Journal Article | autoimmune encephalitis | autoimmune neurology | meningoencephalitis | astrocytes | autoantibodies | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Surgery | Science & Technology | Meningoencephalitis - physiopathology | Glial Fibrillary Acidic Protein - genetics | Brain - diagnostic imaging | Humans | Middle Aged | Movement Disorders - immunology | Male | Plasma Exchange | Ovarian Neoplasms - complications | Cerebellar Ataxia - immunology | Meningoencephalitis - immunology | Young Adult | Autoimmune Diseases of the Nervous System - physiopathology | Carcinoma - complications | Myelitis - immunology | Immunotherapy | Encephalomyelitis - therapy | Aged, 80 and over | Child | Myoclonus - immunology | Myelitis - physiopathology | Spinal Cord - diagnostic imaging | Autoimmune Diseases of the Nervous System - complications | Mice, Knockout | Myelitis - complications | Magnetic Resonance Imaging | Meningoencephalitis - complications | Cerebellar Ataxia - complications | Cerebellar Ataxia - therapy | Movement Disorders - physiopathology | Drug Resistant Epilepsy - immunology | Immunoglobulins, Intravenous - therapeutic use | Protein Isoforms | Adolescent | Drug Resistant Epilepsy - therapy | Mice | Myoclonus - therapy | Glucocorticoids - therapeutic use | Glial Fibrillary Acidic Protein - immunology | Cerebellar Ataxia - physiopathology | Myoclonus - complications | Encephalomyelitis - complications | Encephalomyelitis - physiopathology | Adult | Female | Optic Neuritis - immunology | Optic Neuritis - complications | Optic Neuritis - therapy | Myoclonus - physiopathology | Movement Disorders - complications | Thymus Neoplasms - complications | Autoimmune Diseases of the Nervous System - immunology | Breast Neoplasms - complications | Autoantibodies - immunology | Drug Resistant Epilepsy - complications | Animals | Movement Disorders - therapy | Optic Neuritis - physiopathology | Encephalomyelitis - immunology | Meningoencephalitis - therapy | Aged | Autoimmune Diseases of the Nervous System - therapy | Myelitis - therapy | Thymoma - complications | Drug Resistant Epilepsy - physiopathology | Immunologic Factors - therapeutic use | Autoimmunity | Usage | Care and treatment | Autoantibodies | Autoimmune diseases | Analysis | Encephalitis | Brain | Antigens | Multiple sclerosis | Immunoglobulins | Spinal cord | Dendritic cells | Disease | Epilepsy | Aquaporins | Cognitive ability | Nervous system | Drug resistance | Patients | Proteins | Immunology | Microscopy | Rheumatoid arthritis | Rodents | Ataxia | Animal cognition | Index Medicus
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5. Full Text Restless legs syndrome and periodic leg movements in patients with movement disorders: Specific considerations
by Högl, Birgit and Stefani, Ambra
Movement disorders, ISSN 0885-3185, 05/2017, Volume 32, Issue 5, pp. 669 - 681
sleep | PLM | RLS | polysomnography | Parkinson | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Restless Legs Syndrome - diagnosis | Dystonia - complications | Humans | Essential Tremor - physiopathology | Friedreich Ataxia - physiopathology | Friedreich Ataxia - complications | Essential Tremor - complications | Huntington Disease - physiopathology | Severity of Illness Index | Parkinson Disease - complications | Spinocerebellar Ataxias - complications | Diagnosis, Differential | Restless Legs Syndrome - physiopathology | Nocturnal Myoclonus Syndrome - complications | Dystonia - physiopathology | Nocturnal Myoclonus Syndrome - diagnosis | Spinocerebellar Ataxias - physiopathology | Tourette Syndrome - complications | Parkinson Disease - physiopathology | Polysomnography | Huntington Disease - complications | Movement Disorders - complications | Tourette Syndrome - physiopathology | Movement Disorders - physiopathology | Restless Legs Syndrome - complications | Quality of Life | Nocturnal Myoclonus Syndrome - physiopathology | Restless legs syndrome | Care and treatment | Nervous system diseases | Sleep | Analysis | Movement disorders | Parkinson's disease | Daytime | Neurodegenerative diseases | Insomnia | Cardiovascular diseases | Sleep deprivation | Leg | Index Medicus
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6. Full Text Paroxysmal nonepileptic motor phenomena in newborn
by Orivoli, Sonia and Facini, Carlotta and Pisani, Francesco
Brain & development (Tokyo. 1979), ISSN 0387-7604, 2015, Volume 37, Issue 9, pp. 833 - 839
Neurology | Neonatal seizures | Tremor | Myoclonus | Hyperekplexia | Motor automatisms | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Myoclonus - diagnosis | Humans | Movement Disorders - diagnosis | Electroencephalography | Stiff-Person Syndrome - diagnosis | Tremor - physiopathology | Seizures - physiopathology | Fasciculation - physiopathology | Ocular Motility Disorders - diagnosis | Fasciculation - diagnosis | Stiff-Person Syndrome - physiopathology | Infant, Newborn | Hiccup - physiopathology | Diagnosis, Differential | Brain - physiopathology | Dyskinesias - physiopathology | Dystonia - physiopathology | Seizures - diagnosis | Tremor - diagnosis | Hiccup - diagnosis | Myoclonus - physiopathology | Dystonia - diagnosis | Movement Disorders - physiopathology | Dyskinesias - diagnosis | Ocular Motility Disorders - physiopathology | Infants (Newborn) | Index Medicus
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