Browse Items (5 total)
- Tags: Brain/pathology/physiopathology
Neurologic course of congenital disorders of glycosylation
Tags: 2001, Aspartic Acid/analogs & derivatives/metabolism, Backlog, Brain Diseases, Brain/pathology/physiopathology, Carbohydrate-Deficient Glycoprotein Syndrome/diagnosis, Child, Developmental Disabilities/diagnosis, Epilepsy/diagnosis, Female, Humans, Inborn/diagnosis, Infant, Journal Article, Journal of Child Neurology, Krasnewich D, Lactic Acid/metabolism, Magnetic Resonance Imaging, Magnetic Resonance Spectroscopy, Male, Metabolic, Nerve Degeneration/diagnosis, Neurologic Examination, Pearl PL, Preschool, Q3 Scoping Review Results, Stroke/diagnosis
Hormones and the stressed brain
Infantile neuroaxonal dystrophy (Seitelberger's disease)
Tags: 2002, Auditory, Backlog, Brain Stem/physiology, Brain/pathology/physiopathology, Developmental Medicine and Child Neurology, Diagnosis, Differential, Disease Specific, Electroencephalography, Evoked Potentials, Gordon N, Humans, Journal Article, Magnetic Resonance Imaging, Neuroaxonal Dystrophies/complications/diagnosis, Pantothenate Kinase-Associated Neurodegeneration/diagnosis, Seizures/diagnosis/etiology, Visual/physiology
The natural history of Unverricht-Lundborg disease: a report of eight genetically proven cases
Tags: 2008, Adolescent, Adult, Age Factors, Atrophy/complications/pathology, Auditory, Backlog, Bhatia KP, Brain Stem/physiology, Brain/pathology/physiopathology, Cerebellar Ataxia/complications/diagnosis, Cerebellum/pathology/physiopathology, Chew NK, Child, Chromosomes, Cordivari C, Dementia/complications/diagnosis, Diagnosis, Differential, Disease Progression, Dystonia/complications/diagnosis, Edwards MJ, Electroencephalography, Electromyography, Evoked Potentials, Evoked Potentials/physiology, Female, Human, Humans, Journal Article, Kim HT, Magnetic Resonance Imaging, Male, Martino D, Mir P, Movement Disorders: Official Journal Of The Movement Disorder Society, Myoclonus/complications/diagnosis, Neuropsychological Tests, Pair 21/genetics, Q3 Scoping Review Results, Quinn NP, Schneider SA, Seizures/complications/diagnosis, Severity Of Illness Index, Unverricht-Lundborg Syndrome/diagnosis/genetics/physiopathology
Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations
Tags: 1994, Adolescent, Amino Acid Metabolism Inborn Errors/genetics/physiopathology/therapy, Brain/pathology/physiopathology, Carlsson G, characteristics, Child, Child Preschool, Combined Modality Therapy, Disability Evaluation, Dysarthria/genetics/physiopathology/therapy, Dystonia/genetics/physiopathology/therapy, dystonic-dyskinesia disorder, Female, Fossen A, Glutarates/urine, Glutaric acidemia type I, Glutaryl-CoA Dehydrogenase, Holme I, Humans, hyperkinetic disorder, Infant, Infant Newborn, Intellectual Disability/genetics/physiopathology/therapy, Jellum E, Kyllerman M, Lundberg M, Male, Movement Disorders, Movement Disorders/genetics/physiopathology/therapy, Neurologic Examination, Neuropsychological Tests, Oxidoreductases Acting on CH-CH Group Donors, Oxidoreductases/deficiency, Skjeldal O H, Tomography X-Ray Computed, tone and motor problems, Trajectory, von Dobeln U