Resultados de Pesquisa

INGLÊS

Genetics Of Obesity Syndromes

de I. Sadaf Farooqi, Philip R. Beales e Stephen O'Rahilly

74,19€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Obesity is one of the most important contributing factors to disease throughout the world and is an area of great current interest among researchers and clinicians. The genetics of common obesity is complex, and an important thread through this labyrinth is the study of genetic syndromes in which obesity is a major component.
INGLÊS

Genetic Basis Of Common Diseases

158,99€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Since the first edition of this highly acclaimed text was published in 1992, much new knowledge has been gained about the role of genetic factors in common adult diseases, and we now have a better understanding of the molecular processes involved in genetic susceptibility and diseases mechanisms. The second edition fully incorporates these advances. The entire book has been updated and twelve new chapters have been added. Most of these chapters deal with diseases such as gallstones, osteoporosis, osteoarthritis, skin cancer, other common skin diseases, prostate cancer and migraine headaches that are seen by all physicians. Others address the genetic and molecular basis of spondylarthropathies, lupus, hemochromatosis, IgA deficiency, mental retardation, hearing loss, and the role of mitochondrial variation in adult diseases. Chapters on the evolution of human genetic disease and on animal models add important background on the omplexities of these diseases. Unique clinical applications of genetics to common diseases are covered in the additional new chapters on genetic counseling, pharmacogenetics, and the genetic consequences of modern therapeutics.
INGLÊS

Chromosome Abnormalities And Genetic Counseling

de David Amor e R.J. Mckinlay Gardner

88,76€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Even as classic cytogenetics has given way to molecular karyotyping, and as new deletion and duplication syndromes are identified almost every day, the fundamental role of the genetics clinic remains mostly unchanged. Genetic counselors and medical geneticists explain the "unexplainable," helping families understand why abnormalities occur and whether they''re likely to occur again.Chromosome Abnormalities and Genetic Counseling is the genetics professional''s definitive guide to navigating both chromosome disorders and the clinical questions of the families they impact. Combining a primer on these disorders with the most current approach to their best clinical approaches, this classic text is more than just a reference; it is a guide to how to think about these disorders, even as our technical understanding of them continues to evolve.Completely updated and still infused with the warmth and voice that have made it essential reading for professionals across medical genetics, this edition of Chromosome Abnormalities and Genetic Counseling represents a leap forward in clinical understanding and communication. It is, as ever, essential reading for the field.
INGLÊS

Gardner And Sutherland'S Chromosome Abnormalities And Genetic Counseling

de David Amor e R.J. Mckinlay Gardner

88,76€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Even as classic cytogenetics has given way to molecular karyotyping, and as new deletion and duplication syndromes are identified almost every day, the fundamental role of the genetics clinic remains mostly unchanged. Genetic counselors and medical geneticists explain the "unexplainable," helping families understand why abnormalities occur and whether they''re likely to occur again.Chromosome Abnormalities and Genetic Counseling is the genetics professional''s definitive guide to navigating both chromosome disorders and the clinical questions of the families they impact. Combining a primer on these disorders with the most current approach to their best clinical approaches, this classic text is more than just a reference; it is a guide to how to think about these disorders, even as our technical understanding of them continues to evolve.Completely updated and still infused with the warmth and voice that have made it essential reading for professionals across medical genetics, this edition of Chromosome Abnormalities and Genetic Counseling represents a leap forward in clinical understanding and communication. It is, as ever, essential reading for the field.
INGLÊS

Overgrowth Syndromes - A Clinical Guide

de Giovanni Neri, Luigi Boccuto e Roger E. Stevenson

70,21€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Overgrowth Syndromes is a comprehensive clinical guide to the well-defined genetic disorders (and others that are less well-defined) for which somatic overgrowth is a major manifestation. It details the unique characteristics and known causative genes for this class of disorders, offering clinicians an expert resource for both clinical diagnosis and laboratory confirmation.
INGLÊS

Overgrowth Syndromes - A Clinical Guide

de Giovanni Neri, Luigi Boccuto e Roger E. Stevenson

70,21€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Overgrowth Syndromes is a comprehensive clinical guide to the well-defined genetic disorders (and others that are less well-defined) for which somatic overgrowth is a major manifestation. It details the unique characteristics and known causative genes for this class of disorders, offering clinicians an expert resource for both clinical diagnosis and laboratory confirmation.
INGLÊS

Genetic Skin Disorders

de Virginia P. Sybert

173,56€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 This fully revised and updated edition of GENETIC SKIN DISORDERS reflects the most current understanding of the diagnosis, treatment, genetic basis, and differential diagnoses of inherited skin disorders.
INGLÊS

Epstein'S Inborn Errors Of Development - The Molecular Basis Of Clinical Disorders Of Morphogenesis

397,49€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Epstein's Inborn Errors of Development provides essays on pathways of development and thoughtful reviews of dysmorphic syndromes for which the causative gene has been identified. It is a top-to-bottom revision of the landmark text that both revolutionized and accelerated the field of human genetics.
INGLÊS

Genetic Diseases Of The Eye

de Md Elias I. Traboulsi

233,19€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 This book takes a clinical approach to the patient with a genetic disease that affects the eye. The chapters on particular types of diseases follow the same organizational format, covering history, pathogenesis and etiology, epidemiology, classification, clinical manifestations and diagnosis, and treatment. The recent progress achieved in the molecular genetics of eye disease is fully reflected throughout the book. It is written by leading experts in the field andprovides clinical, molecular genetic and management information on common and rare diseases. The chapters are heavily illustrated and provide a good Atlas for the practicing ophthalmologist or geneticist.
INGLÊS

Human Malformations And Related Anomalies

315,34€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Authored by 40 authorities in genetics and dysmorphology, this streamlined new edition offers an authoritative and richly illustrated guide to clinical presentation, associated anomalies, treatment, and prognosis.
INGLÊS

Duchenne Muscular Dystrophy

de Alan E. H. Emery, Francesco Muntoni e Rosaline C. M. Quinlivan

80,81€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Fully revised and updated the new edition of Duchenne Muscular Dystrophy discusses the recent advances in the field of molecular biology for prenatal diagnosis and genetic counselling to the recent pioneering work with anti-sense oligonucleotides, and the possibility of effective RNA therapy.
INGLÊS

Duchenne Muscular Dystrophy

de Alan E. H. Emery, Francesco Muntoni e Rosaline C. M. Quinlivan

80,81€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Fully revised and updated the new edition of Duchenne Muscular Dystrophy discusses the recent advances in the field of molecular biology for prenatal diagnosis and genetic counselling to the recent pioneering work with anti-sense oligonucleotides, and the possibility of effective RNA therapy.
INGLÊS

Inborn Errors Of Metabolism - From Neonatal Screening To Metabolic Pathways

236,58€ + 10% EM CARTÃO

portes grátis

 This book is an expansion on the known treatment model of IEMs, one that establishes an innovative pathway approach and provides a new authority on this family of disease. Alongside the standard cadre of molecular and clinical underpinnings, this volume includes coverage of newborn screening and an overarching treatment of IEMs as complex diseases - how basic alterations can lead to complex secondary and tertiary effects in metabolism that contribute to increasinglyrecognized natural histories of disease.
INGLÊS

Inborn Errors Of Metabolism - From Neonatal Screening To Metabolic Pathways

121,89€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 This book is an expansion on the known treatment model of IEMs, one that establishes an innovative pathway approach and provides a new authority on this family of disease. Alongside the standard cadre of molecular and clinical underpinnings, this volume includes coverage of newborn screening and an overarching treatment of IEMs as complex diseases - how basic alterations can lead to complex secondary and tertiary effects in metabolism that contribute to increasinglyrecognized natural histories of disease.
INGLÊS

Genomic Medicine - Principles And Practice

185,49€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Preceded by Genomics and clinical medicine / edited by Dhavendra Kumar. (First edition). 2008.
INGLÊS

Genomic Medicine - Principles And Practice

185,49€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 Preceded by Genomics and clinical medicine / edited by Dhavendra Kumar. (First edition). 2008.
INGLÊS

Huntington'S Disease

164,29€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 The fourth edition of the preeminent resource on Huntington's disease is a comprehensive resource on the current knowledge base surrounding this disease. Comprising both updated chapters and seven entirely new chapters, it reflects the major advances that have recently occurred in our understanding of all aspects of this disease.
INGLÊS

Huntington'S Disease

164,29€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 The fourth edition of the preeminent resource on Huntington's disease is a comprehensive resource on the current knowledge base surrounding this disease. Comprising both updated chapters and seven entirely new chapters, it reflects the major advances that have recently occurred in our understanding of all aspects of this disease.
INGLÊS

Hereditary Hearing Loss And Its Syndromes

184,16€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 This is the third edition of the foremost medical reference on genetic hearing loss, updated to include new information on molecular mechanisms. It is an excellent resource for physicians, audiologists, and other professionals working with individuals with hearing loss and their families, and for clinical training programs and researchers in hearing sciences.
INGLÊS

Genomics And Health In The Developing World

ESGOTADO OU NÃO DISPONÍVEL

 This book is designed to be the first major text to discuss advances in medical genetics in the developing world.
INGLÊS

Genomics And Health In The Developing World

242,46€ + 10% EM CARTÃO

DISPONIBILIDADE IMEDIATA

 This book is designed to be the first major text to discuss advances in medical genetics in the developing world.
INGLÊS

Genetic Diseases Of The Eye

~~395,43€~~ 355,89€ 10% IMEDIATO

portes grátis
INGLÊS

Gardner And Sutherland'S Chromosome Abnormalities And Genetic Counseling

de Rj Mckinlay (, University Of Otago) Gardner

158,17€

portes grátis

ESGOTADO OU NÃO DISPONÍVEL
INGLÊS

Overgrowth Syndromes - A Clinical Guide

ESGOTADO OU NÃO DISPONÍVEL

 Overgrowth Syndromes is a comprehensive clinical guide to the well-defined genetic disorders (and others that are less well-defined) for which somatic overgrowth is a major manifestation. It details the unique characteristics and known causative genes for this class of disorders, offering clinicians an expert resource for both clinical diagnosis and laboratory confirmation.
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