Intellectual Disability

ATENDIMENTO EDUCACIONAL ESPECIALIZADO NA MODALIDADE DOMICILIAR: um estudo de caso

Special Education / Inclusive Education / Intellectual Disability

CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592

Genetics / Lebanon / Intellectual Disability / Mental Retardation / Humans / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein

Global developmental delay, osteopenia and ectodermal defect: A new syndrome

Genetics / Social Problems / Intellectual Disability / Brain development / Biopsy / Mental Retardation / Brain / Humans / Child / Genetic Testing / Female / Male / Developmental disabilities / Central Nervous System / Siblings / Skin / Melanocytes / Developmental delay / Syndrome / Sweat glands / Keratins / Skin Biopsy / Mental Retardation / Brain / Humans / Child / Genetic Testing / Female / Male / Developmental disabilities / Central Nervous System / Siblings / Skin / Melanocytes / Developmental delay / Syndrome / Sweat glands / Keratins / Skin Biopsy

Prenatal diagnosis of mitochondrial DNA8993 T----G disease

Intellectual Disability / Biological Sciences / Pregnancy / Mitochondrial DNA / Humans / Mutation / Retinitis pigmentosa / Female / Mothers / Neuromuscular diseases / Prenatal Diagnosis / Syndrome / Mutation / Retinitis pigmentosa / Female / Mothers / Neuromuscular diseases / Prenatal Diagnosis / Syndrome

A new congenital muscular dystrophy with mitochondrial structural abnormalities

Skeletal muscle biology / Adolescent / Intellectual Disability / Humans / Child / Female / Muscular Dystrophies / Male / Disease Progression / Female / Muscular Dystrophies / Male / Disease Progression

A new congenital muscular dystrophy with mitochondrial structural abnormalities

Skeletal muscle biology / Adolescent / Intellectual Disability / Humans / Child / Female / Muscular Dystrophies / Male / Disease Progression / Sarcoplasmic reticulum / Female / Muscular Dystrophies / Male / Disease Progression / Sarcoplasmic reticulum

Oculo-auriculo-vertebral spectrum: Associated anomalies, functional deficits and possible developmental risk factors

Genetics / Eating Disorders / Spine / Speech Disorders / Adolescent / Intellectual Disability / Sweden / Congenital Heart Defects / Prospective studies / Humans / Child / Female / Male / Infant / American / Risk factors / Clinical Sciences / Spectrum / Ear / Risk Factors / Intellectual Disability / Sweden / Congenital Heart Defects / Prospective studies / Humans / Child / Female / Male / Infant / American / Risk factors / Clinical Sciences / Spectrum / Ear / Risk Factors

Importance of retardation and fatigue/interest domains for the diagnosis of major depressive episode after stroke: a four months prospective study Lentificação e fadiga/interesse no diagnóstico do episódio depressivo maior após o acidente vascular cerebral: um estudo prospectivo de quatro meses

Intellectual Disability / Stroke / Prospective studies / Humans / Major Depressive Disorder / Female / Male / Cluster Analysis / Young Adult / Differential Diagnosis / Clinical Sciences / Aged / Middle Aged / Adult / Sex Factors / Mental Fatigue / Female / Male / Cluster Analysis / Young Adult / Differential Diagnosis / Clinical Sciences / Aged / Middle Aged / Adult / Sex Factors / Mental Fatigue

A de novo paradigm for mental retardation

Evolutionary genetics / Intellectual Disability / Biological Sciences / Mental Retardation / Humans / Mutation / Female / Male / Copy Number Variation / Gene Function / Base Sequence / Mutation Rate / Mutation / Female / Male / Copy Number Variation / Gene Function / Base Sequence / Mutation Rate

As mudanças na capacidade e a inclusão da tomada de decisão apoiada a partir do Estatuto da Pessoa com Deficiência AS MUDANÇAS NA CAPACIDADE E A INCLUSÃO DA TOMADA DE DECISÃO APOIADA A PARTIR DO ESTATUTO DA PESSOA COM DEFICIÊNCIA

Intellectual Disability / Disability / Capacidades

Postural stability, tardive dyskinesia and developmental disability

Education / Intellectual Disability / Humans / Female / Male / Posture / Middle Aged / Institutionalization / Postural Balance / Reference Values / Neurologic Examination / Posture / Middle Aged / Institutionalization / Postural Balance / Reference Values / Neurologic Examination

CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592

Genetics / Human Genetics / Lebanon / Molecular Genetics / Intellectual Disability / Mental Retardation / Cytogenetics / Humans / Clinical Genetics / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein / Molecular Sequence Data / Mental Retardation / Cytogenetics / Humans / Clinical Genetics / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein / Molecular Sequence Data

CONTRIBUIÇÕES DA AVALIAÇÃO MEDIADA PARA A ESCOLARIZACÃO DE ALUNOS COM DEFICIÊNCIA INTELECTUAL

Inclusive education (Learning And Teaching) / Inclusive Education / Intellectual Disability / Avaliação em Educação / Discapacidad Intelectual / Special Education Needs and Inclusive Practice / Special and inclusive education / Vigotski / Discapacidad / Educação Inclusiva / Personas Con Discapacidad / Inclusão Escolar / Deficiência Intelectual / Inclusão de pessoas com deficiencia / Special Education Needs and Inclusive Practice / Special and inclusive education / Vigotski / Discapacidad / Educação Inclusiva / Personas Con Discapacidad / Inclusão Escolar / Deficiência Intelectual / Inclusão de pessoas com deficiencia

A escolarização de alunos com deficiência intelectual: políticas, práticas e processos cognitivos

Inclusive education (Learning And Teaching) / Inclusive Education / Intellectual Disability / Discapacidad Intelectual / Special Education Needs and Inclusive Practice / Formação de professores e prática pedagógica / Educação Especial / Educação Inclusiva / Deficiência Intelectual / Processos De Ensino E Aprendizagem / Escolarização / Formação de professores e prática pedagógica / Educação Especial / Educação Inclusiva / Deficiência Intelectual / Processos De Ensino E Aprendizagem / Escolarização

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