Brain development

Algunas consideraciones sobre el impacto de la desnutricion en el desarrollo cerebral, inteligencia y rendimiento escolar

Higher Education / Quality of life / Learning problems / Brain development / Magnetic Resonance / Nutritional Status / Government Policy / Alan / Long Term Effect / Economic Benefit / Magnetic resonance image / Nutritional Status / Government Policy / Alan / Long Term Effect / Economic Benefit / Magnetic resonance image

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Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

Genetics / Pathology / Cognitive Science / Skeletal muscle biology / Magnetic Resonance Imaging / Epilepsy / Histology / Immunohistochemistry / Creatine / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Microcephaly / Female / Muscular Dystrophies / Male / Muscles / Infant / Developmental disabilities / Cataract / D-Aspartic Acid / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Spectrum / Fluorescent Antibody Technique / Family Health / Facies / Adult / Neuromuscular Disorders / Time Factors / Consanguinity / Nuclear Family / Neuronal Migration / Neuropediatrics / Dystrophin / X ray Computed Tomography / Choline / Nuclear Magnetic Resonance Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Nino / Myelin Sheath / Magnetic resonance image / Laminin / Congenital muscular dystrophy / Child preschool / Epilepsy / Histology / Immunohistochemistry / Creatine / Magnetic Resonance Spectroscopy / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Microcephaly / Female / Muscular Dystrophies / Male / Muscles / Infant / Developmental disabilities / Cataract / D-Aspartic Acid / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Spectrum / Fluorescent Antibody Technique / Family Health / Facies / Adult / Neuromuscular Disorders / Time Factors / Consanguinity / Nuclear Family / Neuronal Migration / Neuropediatrics / Dystrophin / X ray Computed Tomography / Choline / Nuclear Magnetic Resonance Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Nino / Myelin Sheath / Magnetic resonance image / Laminin / Congenital muscular dystrophy / Child preschool

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Metabolic encephalopathy in beta-ketothiolase deficiency: The first report from India

Brain development / India / Brain / Humans / Mutation / Male / Infant / X ray Computed Tomography / DNA mutational analysis / Male / Infant / X ray Computed Tomography / DNA mutational analysis

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Progranulin in frontotemporal lobar degeneration and neuroinflammation

Immunology / Dementia / Inflammation / Gene expression / Brain development / Brain / Humans / Mutation / Animals / Neuroinflammation / Microglia / Central Nervous System / Brain injury / Clinical Sciences / Degeneration / Amino Acid Sequence / J / Neurosciences / Full Length Movies / Molecular Sequence Data / Brain / Humans / Mutation / Animals / Neuroinflammation / Microglia / Central Nervous System / Brain injury / Clinical Sciences / Degeneration / Amino Acid Sequence / J / Neurosciences / Full Length Movies / Molecular Sequence Data

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Sulfite oxidase deficiency – An unusual late and mild presentation

Magnetic Resonance Imaging / Brain development / Humans / Mutation / Female / Seizures / Age of Onset / Seizures / Age of Onset

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Gelastic seizures and low-grade hypothalamic astrocytoma: a case report

Polymorphism / Treatment Outcome / Adolescent / Brain development / Brain / Case Report / Humans / Drug Resistance / Male / Mental Disorders / Behavior Problems / Astrocytoma / Cognition disorders / Case Report / Humans / Drug Resistance / Male / Mental Disorders / Behavior Problems / Astrocytoma / Cognition disorders

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Sulfite oxidase deficiency – An unusual late and mild presentation

Magnetic Resonance Imaging / Brain development / Humans / Mutation / Female / Seizures / Age of Onset / Seizures / Age of Onset

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Desarrollo cerebral y asunción de riesgos durante la adolescencia

Social Policy / Risk Taking / Prefrontal Cortex / Brain development / Dopamine / Magnetic Resonance / Cognitive Process / Magnetic Resonance / Cognitive Process

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Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia

Quality of life / Brain development / Mental Retardation / Brain / Humans / Child / Female / Enzyme / Lancet / Brain atrophy / White matter / Valproic Acid / Seizures / Autosomal Recessive / Sodium Benzoate / Dextromethorphan / Breath Test / DNA sequence / Child / Female / Enzyme / Lancet / Brain atrophy / White matter / Valproic Acid / Seizures / Autosomal Recessive / Sodium Benzoate / Dextromethorphan / Breath Test / DNA sequence

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Merosin-positive congenital muscular dystrophy with transient brain dysmyelination, pontocerebellar hypoplasia and mental retardation

Pathology / Cognitive Science / Skeletal muscle biology / Magnetic Resonance Imaging / Epilepsy / Histology / Immunohistochemistry / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Female / Muscular Dystrophies / Male / Muscles / Infant / Cataract / Central Nervous System / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Fluorescent Antibody Technique / Skeletal Muscle / Adult / Neuromuscular Disorders / Time Factors / Scoliosis / Consanguinity / Neuronal Migration / Neuropediatrics / Torticollis / Dystrophin / X ray Computed Tomography / Nuclear Magnetic Resonance Imaging / Mr Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Occipital Lobe / Nino / Myelin Sheath / Histology / Immunohistochemistry / Adolescent / Intellectual Disability / Brain development / Israel / Biopsy / Mental Retardation / London / Brain / Humans / Child / Cerebellum / Muscle / Cerebral Cortex / Haplotypes / Female / Muscular Dystrophies / Male / Muscles / Infant / Cataract / Central Nervous System / Medical Physiology / Pedigree / Creatine Kinase / Genetic linkage analysis / Clinical Sciences / Fluorescent Antibody Technique / Skeletal Muscle / Adult / Neuromuscular Disorders / Time Factors / Scoliosis / Consanguinity / Neuronal Migration / Neuropediatrics / Torticollis / Dystrophin / X ray Computed Tomography / Nuclear Magnetic Resonance Imaging / Mr Imaging / Genetic Markers / Neurosciences / Linkage Analysis / Occipital Lobe / Nino / Myelin Sheath

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Acción directa de la triyodotironina en la expresión génica de cerebro y cerebelo en el período neonatal

Brain development / Psicología

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Developmental vitamin D deficiency causes abnormal brain development

Multiple sclerosis / Schizophrenia / Vitamin D / Brain development / Brain / Humans / Animals / Psychoneuroendocrinology / Animal Model / Vitamin D Deficiency / Humans / Animals / Psychoneuroendocrinology / Animal Model / Vitamin D Deficiency

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Another case of cerebro-facio-thoracic dysplasia (Pascual-Castroviejo syndrome)

Rape / Magnetic Resonance Imaging / Face / Brain development / Mental Retardation / Brain / Pregnancy / Humans / Corpus Callosum / Cerebellum / Female / Thorax / Male / Infant / Differential Diagnosis / Newborn Infant / Adult / Consanguinity / X ray Computed Tomography / Syndrome / Brain / Pregnancy / Humans / Corpus Callosum / Cerebellum / Female / Thorax / Male / Infant / Differential Diagnosis / Newborn Infant / Adult / Consanguinity / X ray Computed Tomography / Syndrome

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Trastorno por déficit de atención con hiperactividad. Una visión global

Sociology / Psychology / Law / Urology / Attention-Deficit/Hyperactivity Disorder / Primary Health Care / Community-Based Mental Health Services / Self Care / Air pollution / Adolescent / Urban Health / Brain development / India / Canada / Psychiatry and the law / Humans / Child / Crime / Behavior Therapy / Chronic Disease / United States / Female / Male / Attention Deficit Disorder / Developmental neuropsychology / Risk factors / Epilepsia / Recurrence / Clinical Sciences / Prevalence / Prisoners / Questionnaires / Adult / Patient Care Team / Public health systems and services research / Sex Factors / Particulate Matter / Developmental Neuropsychology / Risk Factors / Atencion Primaria De La Salud / Methylphenidate / Cross Sectional Studies / New England Journalof Medicine / Neurosciences / Motor vehicles act / Socioeconomic Factors / Primary Health Care / Community-Based Mental Health Services / Self Care / Air pollution / Adolescent / Urban Health / Brain development / India / Canada / Psychiatry and the law / Humans / Child / Crime / Behavior Therapy / Chronic Disease / United States / Female / Male / Attention Deficit Disorder / Developmental neuropsychology / Risk factors / Epilepsia / Recurrence / Clinical Sciences / Prevalence / Prisoners / Questionnaires / Adult / Patient Care Team / Public health systems and services research / Sex Factors / Particulate Matter / Developmental Neuropsychology / Risk Factors / Atencion Primaria De La Salud / Methylphenidate / Cross Sectional Studies / New England Journalof Medicine / Neurosciences / Motor vehicles act / Socioeconomic Factors

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Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency

Magnetic Resonance Imaging / Transcription Regulation / Sequence Analysis / Brain development / Brain / Humans / Cerebellum / Cerebral Cortex / Female / Inborn errors of metabolism / Infant / Skin / Eating / Cortical Development / Clinical Sciences / Newborn Infant / Middle Aged / Agenesis of the Corpus Callosum / White matter / Neuronal Migration / Metabolic Acidosis / Genome sequence / Metabolic pathway / Human Fibroblasts / Humans / Cerebellum / Cerebral Cortex / Female / Inborn errors of metabolism / Infant / Skin / Eating / Cortical Development / Clinical Sciences / Newborn Infant / Middle Aged / Agenesis of the Corpus Callosum / White matter / Neuronal Migration / Metabolic Acidosis / Genome sequence / Metabolic pathway / Human Fibroblasts

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Maternal hypothyroxinemia influences glucose transporter expression in fetal brain and placenta

Endocrinology / Gene expression / Brain development / Animal Production / Brain / Pregnancy / Placenta / Female / Animals / Fetal Growth / Thyroxine / Hypothyroidism / Clinical Sciences / Glucose Transport / Rats / Critical Period / Veterinary Sciences / Glucose Uptake / Thyroid Function / Pregnancy / Placenta / Female / Animals / Fetal Growth / Thyroxine / Hypothyroidism / Clinical Sciences / Glucose Transport / Rats / Critical Period / Veterinary Sciences / Glucose Uptake / Thyroid Function

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