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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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Genetic variants in adipose triglyceride lipase influence lipid levels in familial combined hyperlipidemia

Genetics / Polymorphism / Atherosclerosis / Risk / Adipose tissue / Association study / Humans / Liver / Fatty acids / Haplotypes / Female / Male / Clinical Sciences / Middle Aged / Gene Polymorphism / Family Health / Adult / Fatty Acid / Genetic variation / Lipase / Polymorphisms / Cohort Studies / Association study / Humans / Liver / Fatty acids / Haplotypes / Female / Male / Clinical Sciences / Middle Aged / Gene Polymorphism / Family Health / Adult / Fatty Acid / Genetic variation / Lipase / Polymorphisms / Cohort Studies

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SISTEMA DE INFORMAÇÕES GEOGRÁFICAS PARA A GESTÃO DE PROGRAMAS MUNICIPAIS DE CUIDADO A IDOSOS 1 THE USE OF GEOGRAPHIC INFORMATION SYSTEMS FOR MANAGING MUNICIPAL ELDERLY CARE PROGRAMS SISTEMA DE INFORMACIONES GEOGRÁFICAS PARA LA GESTIÓN DE PROGRAMAS MUNICIPALES DE CUIDADO A ANCIANOS

Public Health / Family Health / Elderly Care / Geographic Information System

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Saúde Mental no contexto da atenção básica: potencialidades, limitações, desafios do Programa Saúde da Família Mental Health in the basic health attention context: potentialities, limitations, challenges in Family Health Program Salud Mental en el contexto de la atención básica: potencialidades

Mental Health / Health Care / Literature Review / Mental Health Care / Family Health / Indexation / Family Health Program / Indexation / Family Health Program

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WORKING WITH F AMILIES WITHIN THE FAMILY HEALTH PROGRAM: NURSE\'S PRACTICE IN MARINGÁ - PARANÁ TRABAJAR CON FAMILIAS EN EL PROGRAMA DE SALUD DE LA FAMILIA: LA PRÁCTICA DEL ENFERMERO EN MARINGÁ - PARANÁ

Health Education / Brazil / Humans / Data Collection / Family Health / Family Nursing / Social Space / Family Health Program / Family Nursing / Social Space / Family Health Program

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A Genetic Risk Score Combining Ten Psoriasis Risk Loci Improves Disease Prediction

Engineering / Genetics / Physics / Chemistry / Biology / Risk / Medicine / Multidisciplinary / Humans / Female / Male / Regression Analysis / Psoriasis / ROC Curve / PLoS one / Family Health / Genotype / Genetic variation / Area Under Curve / Case Control Studies / Risk Score / Risk / Medicine / Multidisciplinary / Humans / Female / Male / Regression Analysis / Psoriasis / ROC Curve / PLoS one / Family Health / Genotype / Genetic variation / Area Under Curve / Case Control Studies / Risk Score

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PROGRAMA SAÚDE DA FAMÍLIA: DESAFIOS E POTENCIALIDADES FRENTE AO USO DE DROGAS FAMILY HEALTH PROGRAM: CHALLENGES AND POTENTIALITIES REGARDING DRUGS USE PROGRAMA SALUD DE LA FAMILIA: DESAFIOS Y POTENCIALIDADES ANTE EL USO DE DROGAS

Primary Health Care / Health Care / Public Health / Drug Use / Problem Solving / Family Health / Revista Eletronica de Enfermagem / Epidemiologic Studies / Drug Related Problems / Health knowledge / Family Health Program / Family Health / Revista Eletronica de Enfermagem / Epidemiologic Studies / Drug Related Problems / Health knowledge / Family Health Program

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Saúde Mental no contexto da atenção básica: potencialidades, limitações, desafios do Programa Saúde da Família Mental Health in the basic health attention context: potentialities, limitations, challenges in Family Health Program Salud Mental en el contexto de la atención básica: potencialidades, ...

Mental Health / Health Care / Literature Review / Mental Health Care / Family Health / Indexation / Family Health Program / Indexation / Family Health Program

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Clinical features of facioscapulohumeral muscular dystrophy 2

Cognitive Science / Neurology / Adolescent / Humans / Child / Muscular Dystrophy / Female / Male / Gender Difference / DNA methylation / Young Adult / Infant / Disease Severity / Phenotype / Chromatin structure / Clinical Sciences / Newborn Infant / Middle Aged / Family Health / Genotype / Adult / Clinical Assessment / Cross sectional Study / Clinical Presentation / Cross Sectional Studies / Neurosciences / Clinical evaluation / Cohort Studies / Muscular Dystrophy / Female / Male / Gender Difference / DNA methylation / Young Adult / Infant / Disease Severity / Phenotype / Chromatin structure / Clinical Sciences / Newborn Infant / Middle Aged / Family Health / Genotype / Adult / Clinical Assessment / Cross sectional Study / Clinical Presentation / Cross Sectional Studies / Neurosciences / Clinical evaluation / Cohort Studies

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Pleiotropic Genetic Effects on LDL Size, Plasma Triglyceride, and HDL Cholesterol in Families

Genetics / Genetic Epidemiology / Risk assessment / Quantitative Genetics / Cardiovascular disease / Vascular biology / Disease susceptibility / Humans / Maximum Likelihood / Female / Male / Genetic determinism / Phenotype / Triglycerides / Clinical Sciences / Aged / Middle Aged / Risk Factor / Family Health / Adult / Particle Size / Size / Risk Assessment / Genetic Analysis / Low Density Lipoprotein (LDL) / Genetic Correlation / Vascular biology / Disease susceptibility / Humans / Maximum Likelihood / Female / Male / Genetic determinism / Phenotype / Triglycerides / Clinical Sciences / Aged / Middle Aged / Risk Factor / Family Health / Adult / Particle Size / Size / Risk Assessment / Genetic Analysis / Low Density Lipoprotein (LDL) / Genetic Correlation

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Antenatal presentation of carnitine palmitoyltransferase II deficiency

Genetics / DNA / Pregnancy / Humans / Kidney / Mutation / Female / Male / Jews / Clinical Sciences / Family Health / Calcinosis / Prenatal Diagnosis / Fetus / Fetal death / Mutation / Female / Male / Jews / Clinical Sciences / Family Health / Calcinosis / Prenatal Diagnosis / Fetus / Fetal death

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A Genetic Risk Score Combining Ten Psoriasis Risk Loci Improves Disease Prediction

Engineering / Genetics / Physics / Chemistry / Biology / Risk / Medicine / Multidisciplinary / Humans / Female / Male / Regression Analysis / Psoriasis / ROC Curve / PLoS one / Family Health / Genotype / Genetic variation / Area Under Curve / Case Control Studies / Risk Score / Risk / Medicine / Multidisciplinary / Humans / Female / Male / Regression Analysis / Psoriasis / ROC Curve / PLoS one / Family Health / Genotype / Genetic variation / Area Under Curve / Case Control Studies / Risk Score

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Activation in Ventral Prefrontal Cortex is Sensitive to Genetic Vulnerability for Attention-Deficit Hyperactivity Disorder

Genetics / Attention-Deficit/Hyperactivity Disorder / Magnetic Resonance Imaging / Adolescent / Gene expression / Prefrontal Cortex / Biological Sciences / Biological Psychiatry / Brain Mapping / Humans / Child / Functional Imaging / Male / Biological / Reaction Time / Inhibitory Control / Children and Adolescents / Family Health / Oxygen / Adult / Clinical Diagnosis / Choice Behavior / Case Control Studies / Prefrontal Cortex / Biological Sciences / Biological Psychiatry / Brain Mapping / Humans / Child / Functional Imaging / Male / Biological / Reaction Time / Inhibitory Control / Children and Adolescents / Family Health / Oxygen / Adult / Clinical Diagnosis / Choice Behavior / Case Control Studies

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Developmental and degenerative features in a complicated spastic paraplegia

Genetics / Magnetic Resonance Imaging / Adolescent / Sequence Analysis / Neurodegenerative Diseases / Oman / Paraplegia / Humans / Female / Male / Young Adult / Proteins / Clinical Sciences / Family Health / Short stature / Adult / Hereditary spastic paraplegia / Annals / Developmental delay / Neurosciences / Quantitative polymerase chain reaction / Oman / Paraplegia / Humans / Female / Male / Young Adult / Proteins / Clinical Sciences / Family Health / Short stature / Adult / Hereditary spastic paraplegia / Annals / Developmental delay / Neurosciences / Quantitative polymerase chain reaction

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Developmental and degenerative features in a complicated spastic paraplegia

Genetics / Magnetic Resonance Imaging / Adolescent / Sequence Analysis / Neurodegenerative Diseases / Oman / Paraplegia / Humans / Female / Male / Young Adult / Proteins / Clinical Sciences / Family Health / Short stature / Adult / Hereditary spastic paraplegia / Annals / Developmental delay / Neurosciences / Quantitative polymerase chain reaction / Oman / Paraplegia / Humans / Female / Male / Young Adult / Proteins / Clinical Sciences / Family Health / Short stature / Adult / Hereditary spastic paraplegia / Annals / Developmental delay / Neurosciences / Quantitative polymerase chain reaction

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A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy

Electroencephalography / Japan / Magnetic Resonance Spectroscopy / Humans / MR spectroscopy / Female / Inborn errors of metabolism / Magnetic Resonance / Central Nervous System / Enzyme / Clinical Sciences / Family Health / Time Factors / Basal ganglia / X ray Computed Tomography / Chromosomes / Protons / Female / Inborn errors of metabolism / Magnetic Resonance / Central Nervous System / Enzyme / Clinical Sciences / Family Health / Time Factors / Basal ganglia / X ray Computed Tomography / Chromosomes / Protons

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