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Abnormalities, Multiple --- Genetic disorders --- Language disorders --- Speech Disorders --- Speech therapists --- Syndromes --- diagnosis --- diagnosis --- diagnosis
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Human genetics --- Pathological physiology. Pathogenesis --- Paediatrics --- Abnormalities --- Developmental disabilities --- Genetic disorders in children --- diagnosis. --- therapy. --- Complications --- Prevention.
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Human genetics --- Medical genetics --- Genetics, Medical --- Genetic Diseases, Inborn --- Génétique médicale --- Periodicals --- Périodiques --- Genetics, Medical. --- Genetic Diseases, Inborn. --- Medical genetics. --- Genetics & Genomics. --- Clinical genetics --- Diseases --- Heredity of disease --- Genetic Diseases --- Genetic Disorders --- Hereditary Disease --- Inborn Genetic Diseases --- Single-Gene Defects --- Hereditary Diseases --- Defect, Single-Gene --- Defects, Single-Gene --- Disease, Genetic --- Disease, Hereditary --- Disease, Inborn Genetic --- Diseases, Genetic --- Diseases, Hereditary --- Diseases, Inborn Genetic --- Disorder, Genetic --- Disorders, Genetic --- Genetic Disease --- Genetic Disease, Inborn --- Genetic Disorder --- Inborn Genetic Disease --- Single Gene Defects --- Single-Gene Defect --- Human Genetics --- Medical Genetics --- Genetics, Human --- Genetic aspects --- medical genetics --- Medical sciences --- Pathology --- Genetic disorders --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Molecular Medicine --- Genetics
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Contents : Diagnosis and Treatment : General Principles. Disorders of Carbohydrate Metabolism. Disorders of Mitochondrial Energy Metabolism. Disorders of Amino Acid Metabolism and Transport. Vitamin-Responsive Disorders. Neurotransmitter and Small Peptide Disorders. Disorders of Lipid and Bile Acid Metabolism. Disorders of Nucleic Acid and Heme Metabolism. Disorders of Metal Transport. Organelle-Related Disorders : Lysosomes, Peroxisomes, and Golgi and Pre-Golgi Systems
Metabolism, Inborn errors of. --- Metabolism, Inborn errors of --- Maladies héréditaires métaboliques --- Diagnosis. --- Treatment --- Diagnostic --- Traitement --- Metabolism, Inborn Errors --- Metabolism, Inborne errors of --- diagnosis. --- therapy. --- Therapy. --- Maladies héréditaires métaboliques --- Hereditary metabolic disorders --- Inborn errors of metabolism --- Genetic disorders --- Metabolism --- diagnosis --- therapy --- Disorders --- Pediatrics. --- Neurology . --- Endocrinology . --- Human genetics. --- Neurology. --- Endocrinology. --- Human Genetics. --- Genetics --- Heredity, Human --- Human biology --- Physical anthropology --- Medicine --- Nervous system --- Neuropsychiatry --- Paediatrics --- Pediatric medicine --- Children --- Internal medicine --- Hormones --- Diseases --- Health and hygiene
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Genetics, Medical. --- Problem-Based Learning. --- Human Genetics --- Medical Genetics --- Genetics, Human --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Genetic Diseases, Inborn --- Molecular Medicine --- Human genetics --- Medical genetics --- Basic Sciences. Genetics --- Genetics (General) --- Genetics (General). --- Genetics, Medical --- Problem-Based Learning --- Problem-Based Curricula --- Active Learning --- Curriculum, Problem-Based --- Experiential Learning --- Curricula, Problem-Based --- Curriculum, Problem Based --- Learning, Active --- Learning, Experiential --- Learning, Problem-Based --- Problem Based Curricula --- Problem Based Learning --- Problem-Based Curriculum --- Clinical genetics --- Diseases --- Heredity of disease --- Medical sciences --- Pathology --- Genetic disorders --- Genetics --- Heredity, Human --- Human biology --- Physical anthropology --- Genetic aspects
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It provides a comprehensive review of public health genetics, including chapters on important general issues such as newborn and other genetic screening, the delivery of genetic services, and the ethical, legal and social implications of the use of genetics within public health. It also reviews relevant clinical topics, the historical background, cross-cultural aspects, and communication issues. Contributors come from a wide range of fields including epidemiology, biostatistics, health policy and management, health services research, behavioral and social sciences, ethics, law, health economics, and laboratory sciences. The first broad survey of the role of genetics in public health, with emphasis on the new molecular genetics. With the accelerating discovery of human genes, public health professionals are increasingly confronted with a large body of scientific information that will guide public health action. Because the broad mission of public health is to fulfill society's interest in assuring conditions in which people can be healthy, the integration of new genetic information in public health research, policy and program development is unavoidable. Public health leadership is urgently needed to use genetic information to improve health and prevent disease, and to address ethical, legal and social issues resulting from inappropriate use of such information. In the not too-distant future, disease prevention and health promotion programs will routinely consider whether or not to use genetic information to help target behavioral, medical or environmental intervention activities in order to maximize benefit and minimize costs and harm to individuals. In anticipation of the expected growth at the interface of genetics and public health, this book delineates a framework for the integration of advances in human genetics into public health practice.
Genetic screening --- Medical genetics --- Public health --- #GBIB:CBMER --- moleculaire genetica --- volksgezondheid --- menselijk genoom --- genetische counseling --- Community health --- Health services --- Hygiene, Public --- Hygiene, Social --- Public health services --- Public hygiene --- Sanitary affairs --- Social hygiene --- Health --- Human services --- Biosecurity --- Health literacy --- Medicine, Preventive --- National health services --- Sanitation --- Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Human chromosome abnormalities --- Medical screening --- génétique moléculaire --- santé publique --- génome humain --- conseil génétique --- Genetic aspects --- Diagnosis --- Genetic screening. --- Medical genetics. --- Public health. --- Public Health. --- Epidemiology, Molecular. --- Genetic Engineering. --- Genetic Predisposition to Disease --- Genetic Screening. --- Genetics, Biochemical. --- Health Planning. --- Preventive Medicine. --- prevention & control.
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This book gives an overview of the potential and the practical details that need to be resolved to make human germline engineering possible. Chapters present the ethical and social concerns and implications of the fast-approaching capability to alter the human germline and take an active role in the future evolution of the species.
Genetic engineering --- Genetic engineering. --- Human cloning --- Human cloning. --- Medical genetics --- Medical genetics. --- Moral and ethical aspects. --- kiemcel (kiemcellijn, embryonale kiemcel, germinale stamcel) --- genetische engineering (manipulatie) --- ethiek (ethische aspecten) --- cellule germinale (lignée germinale, cellule embryonnaire germinale, cellule souche germinale) --- génie génétique (ingénierie, manipulation génétique) --- ethique (aspects ethiques) --- Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Pathology --- Genetic disorders --- Human beings --- Cloning --- Human reproductive technology --- Designed genetic change --- Engineering, Genetic --- Gene splicing --- Genetic intervention --- Genetic surgery --- Genetic recombination --- Biotechnology --- Transgenic organisms --- Moral and ethical aspects --- Genetic aspects
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Genetics --- Genetics, Medical --- Genetic Predisposition to Disease --- Genetic Screening --- Genome --- Medical genetics --- Genomics --- Génétique médicale --- Génomique --- Periodicals. --- Périodiques --- Genomes --- Human genome --- Genetics, Medical. --- Genome. --- Genetic Testing. --- Genetic Predisposition to Disease. --- Genomes. --- Human genome. --- Medical genetics. --- Chemistry --- Health Sciences --- Life Sciences --- Biochemistry --- Pathology --- Predisposition, Genetic --- Susceptibility, Genetic --- Genetic Predisposition --- Genetic Susceptibility --- Genetic Predispositions --- Genetic Susceptibilities --- Predispositions, Genetic --- Susceptibilities, Genetic --- Disease Susceptibility --- Predictive Genetic Testing --- Predictive Testing, Genetic --- Testing, Genetic Predisposition --- Genetic Predisposition Testing --- Genetic Predictive Testing --- Genetic Screenings --- Genetic Testing, Predictive --- Predisposition Testing, Genetic --- Screening, Genetic --- Screenings, Genetic --- Testing, Genetic --- Testing, Genetic Predictive --- Testing, Predictive Genetic --- Human Genetics --- Medical Genetics --- Genetics, Human --- genetics --- diagnosis --- Genetic Testing --- Anticipation, Genetic --- Genetic Association Studies --- Gene-Environment Interaction --- Prenatal Diagnosis --- Preimplantation Diagnosis --- Cytogenetic Analysis --- Molecular Diagnostic Techniques --- Databases, Genetic --- Databases, Nucleic Acid --- Genetic Privacy --- Genes --- Proteome --- Anthropology, Physical --- Chromosome Disorders --- Sex Chromosome Disorders --- Genetic Diseases, Inborn --- Molecular Medicine --- Human chromosomes --- Haploidy --- Clinical genetics --- Diseases --- Heredity of disease --- Human genetics --- Medical sciences --- Genetic disorders --- Genetic aspects
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In 1953 werd door Watson en Crick de structuur van het DNA blootgelegd: dit gaf inzicht in de wijze waarop de erfelijke eigenschappen van een organisme worden 'gecodeerd' en bij elke celdeling doorgegeven. Omstreeks 1975 werd het mogelijk om DNA te 'manipuleren'. De stukjes DNA die een welbepaalde eigenschap tot stand brengen, en die men genen noemt, kan men nu isoleren, identificeren en reproduceren (klonen). In verband met de mens leidt dit samen met andere technieken tot de mogelijkheid om de oorsprong van een groot aantal erfelijke ziekten op te sporen. Door onderzoek van enkele cellen kan men de aanwezigheid van een erfelijke aanleg vaststellen zowel bij de volwassene, het kind, de foetus als bij het embryo. Deze kennis kan heel waardevol zijn, maar ze kan ook ongewenste tot zelfs dramatische gevolgen hebben. Dit boek geeft een inzicht in de mogelijkheden van dit genetisch onderzoek. Tegelijk worden ook de voornaamste ethische vragen gesteld die erdoor worden opgeroepen. (Bron: covertekst)
Human genetics --- Professional ethics. Deontology --- Human medicine --- Erfelijkheidsleer --- Ethique médicale --- Hérédité --- Medische ethiek --- Genetisch onderzoek ; ethiek --- Genetisch onderzoek ; sociale aspecten --- genetica --- erfelijke ziekten --- bio-ethiek --- 174.2 --- 17.023.33 --- 575 --- 061 Ethische problemen --- 094 Biologie --- Erfelijkheid --- Genetica --- 600.2 --- 603.1 --- aangeboren afwijkingen --- erfelijkheidsleer --- ethiek --- genetische diagnose --- genetische test --- maatschappij --- recht --- screening --- 599.2 --- aangeboren afwijkingen (congenitale afwijkingen, hartafwijkingen) --- ethiek (moraal) --- genetisch risico --- prenatale diagnose --- tests --- 010213.jpg --- 61 --- 179.7 --- Beroepsmoraal van de artsen. Medische beroepsethiek --- Génétique --- (zie ook: orthopedie, seksuele ontwikkelingsstoornissen, vaatziekten) --- (zie ook: genetisch advies) --- Conferences - Meetings --- Medical genetics --- Genetic Techniques --- Genetic Counseling --- Genetic Screening --- Moral and ethical aspects --- 174.2 Beroepsmoraal van de artsen. Medische beroepsethiek --- Clinical genetics --- Diseases --- Heredity of disease --- Medical sciences --- Pathology --- Genetic disorders --- Genetic aspects --- Hérédité --- Génétique --- Ethique médicale
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