Movement Disorder

Movimientos anormales identificados en pacientes con tuberculomas intracraneales

Ecuador / Adolescent / Movement disorders / Humans / Child / Female / Male / Young Adult / Central Nervous System / Neurologia / Aged / Adult / Neurología / Movement Disorder / Female / Male / Young Adult / Central Nervous System / Neurologia / Aged / Adult / Neurología / Movement Disorder

Bilateral temporal lobe epilepsy confirmed with intracranial EEG in chorea-acanthocytosis

Psychology / Magnetic Resonance Imaging / Electroencephalography / Positron Emission Tomography / Seizure / Temporal Lobe / Humans / Male / Temporal Lobe Epilepsy / Differential Diagnosis / Clinical Sciences / Single Photon Emission Computed Tomography / Adult / Western blot / Basal ganglia / Epilepsy Surgery / Neurosciences / Movement Disorder / Functional Laterality / Temporal Lobe / Humans / Male / Temporal Lobe Epilepsy / Differential Diagnosis / Clinical Sciences / Single Photon Emission Computed Tomography / Adult / Western blot / Basal ganglia / Epilepsy Surgery / Neurosciences / Movement Disorder / Functional Laterality

Aromatic L-Amino Acid Decarboxylase Deficiency Is a Cause of Long-Fasting Hypoglycemia

Cognitive Science / Neurology / Magnetic Resonance Imaging / Treatment Outcome / Adolescent / Movement disorders / Dopamine / Cerebrospinal Fluid / Brain / Pregnancy / Humans / Child / Hemodynamics / Female / Inborn errors of metabolism / Male / Young Adult / Infant / Follow-up studies / Amniotic Fluid / Differential Diagnosis / Pedigree / Levodopa / Child Neurology / Clinical Sciences / Newborn Infant / European / Longitudinal Studies / Pyridoxine / Adult / Consanguinity / Retrospective Studies / Neuropediatrics / Combination drug therapy / Amino Acid Profile / Biogenic amines / Autosomal Recessive / Clinical Presentation / Neurosciences / Nervous System Diseases / Age of Onset / Movement Disorder / Bromocriptine / Serotonin Uptake Inhibitors / Founder Effect / Medical Treatment / Movement disorders / Dopamine / Cerebrospinal Fluid / Brain / Pregnancy / Humans / Child / Hemodynamics / Female / Inborn errors of metabolism / Male / Young Adult / Infant / Follow-up studies / Amniotic Fluid / Differential Diagnosis / Pedigree / Levodopa / Child Neurology / Clinical Sciences / Newborn Infant / European / Longitudinal Studies / Pyridoxine / Adult / Consanguinity / Retrospective Studies / Neuropediatrics / Combination drug therapy / Amino Acid Profile / Biogenic amines / Autosomal Recessive / Clinical Presentation / Neurosciences / Nervous System Diseases / Age of Onset / Movement Disorder / Bromocriptine / Serotonin Uptake Inhibitors / Founder Effect / Medical Treatment

Anti-N-methyl-D-aspartate receptor encephalitis complicating ovarian teratomas: a case report

Cognitive Science / Neurology / Immunology / Magnetic Resonance Imaging / Archives / Treatment / Adolescent / Pediatric Neurology / Antibodies / Case Report / Humans / Child / Cerebellum / Female / Differential Diagnosis / Arthritis / Anti-inflammatory agents / Clinical Sciences / NMDA / Middle Aged / Adult / Public health systems and services research / Teratoma / Uterus / Encephalitis / Carcinosarcoma / Neuroendocrine Tumors / Neurosciences / Autoantibodies / Movement Disorder / Treatment / Adolescent / Pediatric Neurology / Antibodies / Case Report / Humans / Child / Cerebellum / Female / Differential Diagnosis / Arthritis / Anti-inflammatory agents / Clinical Sciences / NMDA / Middle Aged / Adult / Public health systems and services research / Teratoma / Uterus / Encephalitis / Carcinosarcoma / Neuroendocrine Tumors / Neurosciences / Autoantibodies / Movement Disorder

Aromatic l-amino acid decarboxylase deficiency: An extrapyramidal movement disorder with oculogyric crises

European / Amino Acid Profile / Movement Disorder

Utilidad clínica de la 18FDOPA-PET en trastornos del movimiento. Una revisión sistemática

Positron Emission Tomography / Differential Diagnosis / Systematic review / Movement Disorder

Familial dyskinesia and facial myokymia (FDFM): A novel movement disorder

Adolescent / Movement disorders / Humans / Child / Female / Male / Pedigree / Genetic linkage analysis / Clinical Sciences / Aged / Middle Aged / Adult / Neurosciences / Movement Disorder / Male / Pedigree / Genetic linkage analysis / Clinical Sciences / Aged / Middle Aged / Adult / Neurosciences / Movement Disorder

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

Genetics / Epilepsy / Adolescent / Intellectual Disability / Mental Retardation / Cerebrospinal Fluid / Brain / Humans / Child / Blood Glucose / Mutation / Female / Male / Young Adult / Infant / Phenotype / Glucose Transport / Spectrum / Adult / Clinical Data / Retrospective Studies / Syndrome / Translation initiation / Age of Onset / Data Type / Movement Disorder / Ketogenic diet / Cerebrospinal Fluid / Brain / Humans / Child / Blood Glucose / Mutation / Female / Male / Young Adult / Infant / Phenotype / Glucose Transport / Spectrum / Adult / Clinical Data / Retrospective Studies / Syndrome / Translation initiation / Age of Onset / Data Type / Movement Disorder / Ketogenic diet

Biochemical alteration in cerebrospinal fluid precedes behavioral deficits in Parkinsonian rats induced by 6-hydroxydopamine

Dopamine / Cerebrospinal Fluid / Animals / Male / Cell Death / Substantia nigra / Neurons / Tyrosine Hydroxylase / Clinical Sciences / Rats / Biological markers / Hypokinesia / Somatic Cell Count / Neurosciences / Movement Disorder / Substantia nigra / Neurons / Tyrosine Hydroxylase / Clinical Sciences / Rats / Biological markers / Hypokinesia / Somatic Cell Count / Neurosciences / Movement Disorder

Guanidinoacetate methyltransferase deficiency: New clinical features

Magnetic Resonance Spectroscopy / Pediatric Neurology / Basal ganglia / Developmental delay / Neurosciences / Movement Disorder

Deficiencia cerebral de creatina: primeros pacientes españoles con mutaciones en el gen GAMT

Creatine / Magnetic Resonance Spectroscopy / Adolescent / Language Disorder / Spain / Mental Retardation / Humans / Child / Mutation / Female / Inborn errors of metabolism / Male / Middle Aged / Treatment Response / Medicina Clinica / Movement Disorder / Mental Retardation / Humans / Child / Mutation / Female / Inborn errors of metabolism / Male / Middle Aged / Treatment Response / Medicina Clinica / Movement Disorder

Deficiencia cerebral de creatina: primeros pacientes españoles con mutaciones en el gen GAMT

Creatine / Magnetic Resonance Spectroscopy / Adolescent / Language Disorder / Spain / Mental Retardation / Humans / Child / Mutation / Female / Inborn errors of metabolism / Male / Middle Aged / Treatment Response / Medicina Clinica / Movement Disorder / Mental Retardation / Humans / Child / Mutation / Female / Inborn errors of metabolism / Male / Middle Aged / Treatment Response / Medicina Clinica / Movement Disorder

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