Pediatric Neurology

Free amino acids of CSF in hypoxicischemic encephalopathy

Pediatric Neurology / Neurosciences

Intracranial hemorrhage due to vitamin K deficiency

Pediatrics / Pediatric Neurology

Free amino acids of CSF in hypoxicischemic encephalopathy

Pediatric Neurology / Neurosciences

Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy

Magnetic Resonance Imaging / Treatment / Pediatric Neurology / Humans / Correlation / Male / Differential Diagnosis / Phenotype / Gas Chromatography/mass Spectrometry / Neurosciences / Brain Damage / Riboflavin / Nino / Magnetic resonance image / Male / Differential Diagnosis / Phenotype / Gas Chromatography/mass Spectrometry / Neurosciences / Brain Damage / Riboflavin / Nino / Magnetic resonance image

Medulloblastoma or cerebellar dysplastic gangliocytoma (Lhermitte-Duclos disease)?

Magnetic Resonance Imaging / Pediatric Neurology / Humans / Cerebellum / Medulloblastoma / Male / Infant / Differential Diagnosis / Gadolinium / Ganglioneuroma / Drug Therapy / X ray Computed Tomography / Neurosciences / Male / Infant / Differential Diagnosis / Gadolinium / Ganglioneuroma / Drug Therapy / X ray Computed Tomography / Neurosciences

Reversible deafness caused by biotinidase deficiency

Pediatric Neurology / Humans / Male / Infant / Hearing Loss / Biotin / Deafness / Consanguinity / Neurosciences / Biotin / Deafness / Consanguinity / Neurosciences

Fatal infantile mitochondrial encephalomyopathy with complex I and IV deficiencies

Electron Microscopy / Pediatric Neurology / Biopsy / Humans / Male / Muscles / Infant / Follow-up studies / Newborn Infant / L-carnitine / Amino Acids / Neurosciences / Muscles / Infant / Follow-up studies / Newborn Infant / L-carnitine / Amino Acids / Neurosciences

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

Trastorno por déficit de atención con hiperactividad. Una visión global

Psychology / Law / Psychiatry / Urology / Attention-Deficit/Hyperactivity Disorder / Treatment Outcome / Adolescent / Brain development / Pediatric Neurology / Psychiatry and the law / Traditional Chinese Medicine / Humans / Child / Attention Deficit Disorder / Developmental neuropsychology / Publication Bias / Epilepsia / Autism Spectrum Disorder / Clinical Sciences / Children and Adolescents / Spectrum / Public health systems and services research / Time Factors / Developmental Neuropsychology / Attention Disorders / Asperger Syndrome / Atencion Primaria De La Salud / Methylphenidate / New England Journalof Medicine / Neurosciences / Treatment Outcome / Adolescent / Brain development / Pediatric Neurology / Psychiatry and the law / Traditional Chinese Medicine / Humans / Child / Attention Deficit Disorder / Developmental neuropsychology / Publication Bias / Epilepsia / Autism Spectrum Disorder / Clinical Sciences / Children and Adolescents / Spectrum / Public health systems and services research / Time Factors / Developmental Neuropsychology / Attention Disorders / Asperger Syndrome / Atencion Primaria De La Salud / Methylphenidate / New England Journalof Medicine / Neurosciences

Radial Microcolumnar Cortical Architecture: Maturational Arrest or Cortical Dysplasia?

Malformations of Cortical Development / Pediatric Neurology / Cell Differentiation / Humans / Cerebral Cortex / Animals / Cell cycle checkpoints / Neurosciences / Animals / Cell cycle checkpoints / Neurosciences

Reversible deafness caused by biotinidase deficiency

Pediatric Neurology / Humans / Male / Infant / Hearing Loss / Biotin / Deafness / Consanguinity / Neurosciences / Biotin / Deafness / Consanguinity / Neurosciences

Carbamyl phosphate synthetase 1 deficiency: A destructive encephalopathy

Magnetic Resonance Imaging / Evolution / Pediatric Neurology / Brain / Humans / Female / Infant / Differential Diagnosis / Enzyme / Atrophy / Urea Cycle / Deficiency / X ray Computed Tomography / Deficit / Nuclear Magnetic Resonance Imaging / Neurosciences / hyperammonemia / Female / Infant / Differential Diagnosis / Enzyme / Atrophy / Urea Cycle / Deficiency / X ray Computed Tomography / Deficit / Nuclear Magnetic Resonance Imaging / Neurosciences / hyperammonemia

Carbamyl phosphate synthetase 1 deficiency: A destructive encephalopathy

Magnetic Resonance Imaging / Evolution / Pediatric Neurology / Brain / Humans / Female / Infant / Differential Diagnosis / Enzyme / Atrophy / Urea Cycle / Deficiency / X ray Computed Tomography / Deficit / Nuclear Magnetic Resonance Imaging / Neurosciences / hyperammonemia / Female / Infant / Differential Diagnosis / Enzyme / Atrophy / Urea Cycle / Deficiency / X ray Computed Tomography / Deficit / Nuclear Magnetic Resonance Imaging / Neurosciences / hyperammonemia

Guanidinoacetate methyltransferase deficiency: New clinical features

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

Mitochondrial activity in pompe’s disease

Electron Microscopy / Mitochondria / Pediatric Neurology / Biopsy / Humans / Female / Muscles / Infant / Mitochondrial Respiratory Chain / Differential Diagnosis / Electron Transport / Enzyme / Newborn Infant / Skeletal Muscle / Specific Activity / Enzyme activity / Glycogen / Neurosciences / Oxidation-Reduction / Citrate Synthase / Clinical Diagnosis / Oxidative Metabolism / Female / Muscles / Infant / Mitochondrial Respiratory Chain / Differential Diagnosis / Electron Transport / Enzyme / Newborn Infant / Skeletal Muscle / Specific Activity / Enzyme activity / Glycogen / Neurosciences / Oxidation-Reduction / Citrate Synthase / Clinical Diagnosis / Oxidative Metabolism

Mitochondrial complex i deficiency in a female with multiplex arthrogryposis congenita

Skeletal muscle biology / Mitochondria / Energy Metabolism / Pediatric Neurology / Biopsy / Humans / Child / Female / Specific Activity / Oxidative phosphorylation / Neurosciences / Arthrogryposis / Humans / Child / Female / Specific Activity / Oxidative phosphorylation / Neurosciences / Arthrogryposis

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