Behavioural Problems in Developmental Disorders: A Paediatricians Guide helps paediatricians better understand and manage behaviour issues in children and adolescents with developmental disorders. These challenges are common but often not well cover...Loe edasi...
Behavioural Problems in Developmental Disorders: A Paediatricians Guide helps paediatricians better understand and manage behaviour issues in children and adolescents with developmental disorders. These challenges are common but often not well cover...Loe edasi...
(Ilmumisaeg: 25-Mar-2025, EPUB+DRM, Kirjastus: Simon & Schuster, ISBN-13: 9781668063569)
Unlock the secret to longevity with Dr. Stephanie Venn-Watsons ;groundbreaking, once-in-a-century discovery (Mark Hyman, MD, New York Times bestselling author) of the molecule C15:0an essential fat found in whole milk, cheese, and fatty fishthat c...Loe edasi...
"e;Part genetics primer and part memoir, this is a richly compelling read."e; - BooklistMy niece was 36, newly married, and "e;on top of the world,"e; when she collapsed and died. Her autopsy report caused us to panic-there was someth...Loe edasi...
"e;Part genetics primer and part memoir, this is a richly compelling read."e; - BooklistMy niece was 36, newly married, and "e;on top of the world,"e; when she collapsed and died. Her autopsy report caused us to panic-there was someth...Loe edasi...
(Ilmumisaeg: 15-Nov-2024, PDF+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781040285985)
Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. The book focuses on DNA mutations which give rise to abnormalities of protein structure and function in genetic disease....Loe edasi...
(Ilmumisaeg: 15-Nov-2024, EPUB+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781040282274)
Recent years have seen rapid advances in our understanding of genetic diseases in terms of their molecular origins. The book focuses on DNA mutations which give rise to abnormalities of protein structure and function in genetic disease....Loe edasi...
Epigenetics in Human Disease, Third Edition examines the diseases and conditions on which we have advanced knowledge of epigenetic mechanisms, such as cancer, autoimmune disorders, aging, metabolic disorders, neurobiological disorders and cardiovascu...Loe edasi...
Epigenetics in Human Disease, Third Edition examines the diseases and conditions on which we have advanced knowledge of epigenetic mechanisms, such as cancer, autoimmune disorders, aging, metabolic disorders, neurobiological disorders and cardiovascu...Loe edasi...
Genetic Steroid Disorders, Second Edition targets adult and pediatric endocrinologists, clinical geneticists, genetic counselors, reproductive endocrinologists, neonatologists, urologists, and psychoendocrinologists. It is designed to assist these sp...Loe edasi...
Genetic Steroid Disorders, Second Edition targets adult and pediatric endocrinologists, clinical geneticists, genetic counselors, reproductive endocrinologists, neonatologists, urologists, and psychoendocrinologists. It is designed to assist these sp...Loe edasi...
This book explores the basic concepts of genetics and heredity in human diseases. It discusses techniques like RT-PCR, karyotyping, DNA/RNA extraction, RFLP, DNA sequencing and electrophoresis, which will be helpful in clinical diagnostics for patien...Loe edasi...
This book describes the historical context of colorectal cancer predisposition syndromes and the latest knowledge relating to each of the known hereditary colorectal cancer predisposition syndromes. There is a particular focus on the management of ea...Loe edasi...
Kim Zeidler hat Psoriasis, seitdem sie 4 Jahre alt ist. Das erste Mal kurze Hosen trug sie allerdings erst mit 30, weil sie sich für die weißen Flecken auf ihrer Haut, die die Schuppenflechte verursacht, so geschämt hat. Dank des positiven Zuspruc...Loe edasi...
Kim Zeidler hat Psoriasis, seitdem sie 4 Jahre alt ist. Das erste Mal kurze Hosen trug sie allerdings erst mit 30, weil sie sich für die weißen Flecken auf ihrer Haut, die die Schuppenflechte verursacht, so geschämt hat. Dank des positiven Zuspruc...Loe edasi...
Kathy Steligo, Sue Friedman, Allison W. Kurian, Matthew Boland Yurgelun
(Ilmumisaeg: 27-Sep-2022, PDF+DRM, Kirjastus: Johns Hopkins University Press, ISBN-13: 9781421444277)
The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality of life, and more.Up to 10 percent of cancers are caused by inherited mutations in specific ge...Loe edasi...
Kathy Steligo, Sue Friedman, Allison W. Kurian, Matthew Boland Yurgelun
(Ilmumisaeg: 27-Sep-2022, EPUB+DRM, Kirjastus: Johns Hopkins University Press, ISBN-13: 9781421444277)
The most comprehensive guide available on hereditary cancers, from understanding risk, prevention, and genetic counseling and testing to treatment, quality of life, and more.Up to 10 percent of cancers are caused by inherited mutations in specific ge...Loe edasi...
(Ilmumisaeg: 12-May-2022, PDF+DRM, Kirjastus: Oxford University Press, ISBN-13: 9780192593290)
Containing concise, updated, and easy-to-use summaries on a comprehensive range of clinical scenarios and conditions encountered by paediatricians and multi-disciplinary professionals in their everyday practice, this new edition of Neurodisability an...Loe edasi...
(Ilmumisaeg: 12-May-2022, EPUB+DRM, Kirjastus: Oxford University Press, ISBN-13: 9780192593306)
Containing concise, updated, and easy-to-use summaries on a comprehensive range of clinical scenarios and conditions encountered by paediatricians and multi-disciplinary professionals in their everyday practice, this new edition of Neurodisability an...Loe edasi...
(Ilmumisaeg: 01-Jul-2021, MP3, Kirjastus: Random House, ISBN-13: 9781473597167)
Brought to you by Penguin.Welcome to a revolution in the science of human health. Imagine...- Knowing years in advance whether you are likely to get certain cancers- Having a bespoke understanding of your individual genes, organs and cells- Following...Loe edasi...
A big-picture forecast of how medicine stands on the threshold of a revolution that will radically change all of our lives The TimesWelcome to a revolution in the science of you. This landmark new book from award-winning scientist Daniel M. Davis e...Loe edasi...
(Ilmumisaeg: 05-Jan-2021, PDF+DRM, Kirjastus: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, ISBN-13: 9783662624500)
Dieses Buch analysiert die Rechtslage im Hinblick auf die heterologe Insemination in Deutschland, Österreich und der Schweiz. Den Schwerpunkt bildet dabei die Untersuchung des im Jahre 2018 in Deutschland in Kraft getretenen Samenspenderregiste...Loe edasi...
(Ilmumisaeg: 05-Jan-2021, EPUB+DRM, Kirjastus: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, ISBN-13: 9783662624500)
Dieses Buch analysiert die Rechtslage im Hinblick auf die heterologe Insemination in Deutschland, Österreich und der Schweiz. Den Schwerpunkt bildet dabei die Untersuchung des im Jahre 2018 in Deutschland in Kraft getretenen Samenspenderregiste...Loe edasi...
(Ilmumisaeg: 17-Dec-2020, PDF+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781000102277)
Many common diseases are partly attributable to the genes which an individual inherits. Early steps have now been made in developing ways to determine which genetic variations are important, with some recent successes. This is a collection of papers...Loe edasi...
(Ilmumisaeg: 17-Dec-2020, EPUB+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781000144581)
Many common diseases are partly attributable to the genes which an individual inherits. Early steps have now been made in developing ways to determine which genetic variations are important, with some recent successes. This is a collection of papers...Loe edasi...
Katharina Beier, Claudia Brügge, Petra Thorn, Claudia Wiesemann
Sari: Medicine (German Language)
(Ilmumisaeg: 19-Feb-2020, PDF+DRM, Kirjastus: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, ISBN-13: 9783662602980)
Sammelband mit Beiträgen von 28 Expertinnen und Experten aus dem Bereich der assistierten Reproduktion.Immer häufiger werden Verfahren der medizinisch assistierten Reproduktion genutzt, die den Beitrag Dritter einschließen, also Samenspe...Loe edasi...
Katharina Beier, Claudia Brügge, Petra Thorn, Claudia Wiesemann
Sari: Medicine (German Language)
(Ilmumisaeg: 19-Feb-2020, EPUB+DRM, Kirjastus: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG, ISBN-13: 9783662602980)
Sammelband mit Beiträgen von 28 Expertinnen und Experten aus dem Bereich der assistierten Reproduktion.Immer häufiger werden Verfahren der medizinisch assistierten Reproduktion genutzt, die den Beitrag Dritter einschließen, also Samenspe...Loe edasi...
Genetic testing has provided important clues to understanding our health, but it has also raised many ethical, legal, and medical questions and concerns. This book explores the breadth of genetic testing, its possibilities, and the controversies that...Loe edasi...
Genetic testing has provided important clues to understanding our health, but it has also raised many ethical, legal, and medical questions and concerns. This book explores the breadth of genetic testing, its possibilities, and the controversies that...Loe edasi...
Genetic testing has provided important clues to understanding our health, but it has also raised many ethical, legal, and medical questions and concerns. This book explores the breadth of genetic testing, its possibilities, and the controversies that...Loe edasi...
(Ilmumisaeg: 19-Dec-2019, PDF+DRM, Kirjastus: Oxford University Press, ISBN-13: 9780192543905)
Clinicians and scientists are increasingly recognising the importance of an evolutionary perspective in studying the aetiology, prevention, and treatment of human disease; the growing prominence of genetics in medicine is further adding to the intere...Loe edasi...
A NEW YORK TIMES BESTSELLER ;Brilliant and enthralling. The Wall Street Journal A paradigm-shifting book from an acclaimed Harvard Medical School scientist and one of Times most influential people.Its a seemingly undeniable truth that aging is i...Loe edasi...
(Ilmumisaeg: 29-Jul-2019, EPUB+DRM, Kirjastus: Oxford University Press Inc, ISBN-13: 9780190940393)
International uproar followed the recent announcement of the birth of twin girls whose genomes had been edited with a breakthrough DNA editing-technology. This technology, called clustered regularly interspaced short palindrome repeats or CRISPR-Cas9...Loe edasi...
(Ilmumisaeg: 29-Jul-2019, PDF+DRM, Kirjastus: Oxford University Press Inc, ISBN-13: 9780190940386)
International uproar followed the recent announcement of the birth of twin girls whose genomes had been edited with a breakthrough DNA editing-technology. This technology, called clustered regularly interspaced short palindrome repeats or CRISPR-Cas9...Loe edasi...
Noonan Syndrome: Characteristics and Interventions provides an in-depth analysis on this disorder that pediatric endocrinologists and primary care clinicians can use to make sure they provide affected patients with an updated model of care and approp...Loe edasi...
Noonan Syndrome: Characteristics and Interventions provides an in-depth analysis on this disorder that pediatric endocrinologists and primary care clinicians can use to make sure they provide affected patients with an updated model of care and approp...Loe edasi...
(Ilmumisaeg: 07-May-2019, PDF+DRM, Kirjastus: Thomas Nelson Publishers, ISBN-13: 9781418599355)
Jamie Tyrone tenía cuarenta y nueve años cuando se enteró de que poseía una predisposición genética al Mal de Alzheimer. De hecho, sus genes arrojaron un 91 de probabilidad de contraer la enfermedad duran...Loe edasi...
(Ilmumisaeg: 07-May-2019, EPUB+DRM, Kirjastus: Thomas Nelson Publishers, ISBN-13: 9781418599355)
Jamie Tyrone tenía cuarenta y nueve años cuando se enteró de que poseía una predisposición genética al Mal de Alzheimer. De hecho, sus genes arrojaron un 91 de probabilidad de contraer la enfermedad duran...Loe edasi...
Supported by figures, tables and photos, this book illustrates the basics of genetic diagnostics, prenatal and reproductive medicine, syndromology and familial cancers. It also includes numerous illustrated examples of the most frequent genetic disea...Loe edasi...
Molecular Chaperones in Human Disorders, Volume 114 in the Advances in Protein Chemistry and Structural Biology series, provides an overview of current developments in mechanisms underlying DNA repair and their involvement in maintaining chromatin re...Loe edasi...
Molecular Chaperones in Human Disorders, Volume 114 in the Advances in Protein Chemistry and Structural Biology series, provides an overview of current developments in mechanisms underlying DNA repair and their involvement in maintaining chromatin re...Loe edasi...
Sari: Advances in Experimental Medicine and Biology
(Ilmumisaeg: 21-Dec-2018, PDF+DRM, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319950464)
This Atlas of Inherited Retinal Disorders provides a thorough overview of various inherited retinal dystrophies with emphasis on phenotype characteristics and how they relate to the most frequently encountered genes. It also meets the previously unme...Loe edasi...
Sari: Advances in Experimental Medicine and Biology
(Ilmumisaeg: 21-Dec-2018, EPUB+DRM, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319950464)
This Atlas of Inherited Retinal Disorders provides a thorough overview of various inherited retinal dystrophies with emphasis on phenotype characteristics and how they relate to the most frequently encountered genes. It also meets the previously unme...Loe edasi...
This book describes newborn screening as a public health program for the early detection of genetic disorders.It presents the recommended uniform screening panel (RUSP), a list of genetic disorders recommended by the U.S. government for states to inc...Loe edasi...
This book describes newborn screening as a public health program for the early detection of genetic disorders.It presents the recommended uniform screening panel (RUSP), a list of genetic disorders recommended by the U.S. government for states to inc...Loe edasi...
(Ilmumisaeg: 07-Nov-2018, PDF+DRM, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319980652)
This invaluable resource discusses insights ranging from basic biological mechanisms of various types of stem cells through the potential applications in the treatment of human diseases, including cancer and genetic disorders. These discoveries...Loe edasi...
(Ilmumisaeg: 07-Nov-2018, EPUB+DRM, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319980652)
This invaluable resource discusses insights ranging from basic biological mechanisms of various types of stem cells through the potential applications in the treatment of human diseases, including cancer and genetic disorders. These discoveries...Loe edasi...
(Ilmumisaeg: 26-Sep-2018, PDF+DRM, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319945712)
This text provides a concise yet comprehensive overview of Alagille syndrome. The book reviews the pathophysiology and genetics of the disorder, discusses recent molecular advances and its impact on diagnostics, and describes management challenges an...Loe edasi...
(Ilmumisaeg: 26-Sep-2018, EPUB+DRM, Kirjastus: Springer International Publishing AG, ISBN-13: 9783319945712)
This text provides a concise yet comprehensive overview of Alagille syndrome. The book reviews the pathophysiology and genetics of the disorder, discusses recent molecular advances and its impact on diagnostics, and describes management challenges an...Loe edasi...
