Infant - Page 19 | DATOSPDF

Evaluación de un servicio telefónico de prevención y promoción de salud infantil antes de su puesta en funcionamiento

Health Promotion / Focus Groups / Health Care / Consumer Behavior / Spain / Information Services / Humans / Child / Health information / Infant / Information Service / Vaccination / Parents / Adult / Time Factors / Consumer Participation / Planning Techniques / Hotlines / Child Rearing / Preventive Health Services / Child Health Services / Information Services / Humans / Child / Health information / Infant / Information Service / Vaccination / Parents / Adult / Time Factors / Consumer Participation / Planning Techniques / Hotlines / Child Rearing / Preventive Health Services / Child Health Services

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Determinación de valores normalizados del desplazamiento sistólico del plano del anillo tricúspide (tapse) en pacientes colombianos sin comorbilidades

Mineral Processing / Adolescent / Prospective studies / Humans / Child / Female / Male / Infant / Newborn Infant / Children and Adolescents / Right Ventricle / Reference Values / Reference Value / Female / Male / Infant / Newborn Infant / Children and Adolescents / Right Ventricle / Reference Values / Reference Value

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Efficacy of emergency room thoracotomy in pediatric trauma

Adolescent / Humans / Child / Emergency Room / Female / Resuscitation / Male / Pediatric Surgery / Infant / Pediatric / Clinical Sciences / Thoracic Surgery / Resuscitation / Male / Pediatric Surgery / Infant / Pediatric / Clinical Sciences / Thoracic Surgery

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One-year experience in a regional pediatric trauma center

Pediatrics / Adolescent / Plastic and Reconstructive Surgery / Prospective studies / Humans / Child / Female / Male / Pediatric Surgery / Infant / Pediatric / Maryland / Clinical Sciences / Newborn Infant / Pediatric Orthopaedics / Wounds and Injuries / Child / Female / Male / Pediatric Surgery / Infant / Pediatric / Maryland / Clinical Sciences / Newborn Infant / Pediatric Orthopaedics / Wounds and Injuries

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Congenital Darier disease

Humans / Female / Male / Infant / Skin / Pedigree / Clinical Sciences / Family Health / Darier Disease / Pedigree / Clinical Sciences / Family Health / Darier Disease

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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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Secondary reduction of α7B integrin in laminin α2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle

Skeletal muscle biology / Aging / Adolescent / Extracellular Matrix / Antibodies / Humans / Child / Mice / Muscular Dystrophy / Muscular Dystrophies / Animals / Infant / Alternative splicing / The / Integrins / Clinical Sciences / Newborn Infant / Skeletal Muscle / Adult / Muscle development / Alternative Splicing / Protein isoforms / Fetus / Muscle Function / Amino Acid Sequence / Dystrophin / Neurosciences / Becker Muscular Dystrophy (BMD) / Knock Out Mice / Humans / Child / Mice / Muscular Dystrophy / Muscular Dystrophies / Animals / Infant / Alternative splicing / The / Integrins / Clinical Sciences / Newborn Infant / Skeletal Muscle / Adult / Muscle development / Alternative Splicing / Protein isoforms / Fetus / Muscle Function / Amino Acid Sequence / Dystrophin / Neurosciences / Becker Muscular Dystrophy (BMD) / Knock Out Mice

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Internal jugular phlebectasia in Menkes disease

Humans / Male / Infant / Pediatric / Clinical Sciences / Magnetic resonance angiography

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Congenital Tuberculosis: A Case Report

Treatment Outcome / Risk assessment / Adolescent / Tuberculosis / Pregnancy / Case Report / Humans / Mycobacterium tuberculosis / Female / Male / Sepsis / Infant / Follow-up studies / Differential Diagnosis / Lung / Newborn Infant / Adult / Risk Assessment / Pulmonary Tuberculosis / Pregnancy Outcome / Maternal-fetal exchange / Clinical Nutrition in Pediatrics / Case Report / Humans / Mycobacterium tuberculosis / Female / Male / Sepsis / Infant / Follow-up studies / Differential Diagnosis / Lung / Newborn Infant / Adult / Risk Assessment / Pulmonary Tuberculosis / Pregnancy Outcome / Maternal-fetal exchange / Clinical Nutrition in Pediatrics

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Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts

Electron Microscopy / DNA / Mitochondrial DNA / Humans / Clinical / Male / Infant / Electron Transport / nuclear DNA / Newborn Infant / Cell nucleus / Hybrid Solar Cells / Human Fibroblasts / Clinical Investigation / Male / Infant / Electron Transport / nuclear DNA / Newborn Infant / Cell nucleus / Hybrid Solar Cells / Human Fibroblasts / Clinical Investigation

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Cytochrome c Oxidase Deficiency

Molecular Biology / Mitochondrial DNA / Humans / Child / Cytochrome c oxidase / Infant / Pediatric / Brain Diseases / Infant / Pediatric / Brain Diseases

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Infantile citrullinemia caused by citrin deficiency with increased dibasic amino acids

Molecular Genetics / Humans / Male / Infant / Membrane transport proteins / Clinical Sciences / Breast milk / Human Milk / Amino Acid Profile / Human Fibroblasts / Genome Duplication / Clinical Sciences / Breast milk / Human Milk / Amino Acid Profile / Human Fibroblasts / Genome Duplication

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Paradoxical cerebral arterial gas embolism: Computed tomography findings

Computed Tomography / Humans / Male / Infant / Clinical Sciences

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Biopterin responsive phenylalanine hydroxylase deficiency

Genetics / Adolescent / Humans / Child / Female / Phenylketonuria / Male / Infant / Enzyme / Clinical Sciences / Pilot study / Spectrum / Adult / Phenylalanine / Autosomal Recessive / Phenylalanine hydroxylase / Tyrosine / Phenylketonuria / Male / Infant / Enzyme / Clinical Sciences / Pilot study / Spectrum / Adult / Phenylalanine / Autosomal Recessive / Phenylalanine hydroxylase / Tyrosine

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Lipoamide dehydrogenase deficiency with primary lactic acidosis: Favorable response to treatment with oral lipoic acid

Pediatrics / Humans / Male / Infant / The / Skin / Acidosis / Human Fibroblasts / Skin / Acidosis / Human Fibroblasts

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Copper deficiency in infants fed cow milk

Pediatrics / Humans / Copper / Female / Animals / Male / Infant / Milk / Cattle / Copper Deficiency / Male / Infant / Milk / Cattle / Copper Deficiency

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