Practical Guide to Neurogenetics E Book

Practical Guide to Neurogenetics E Book
Author: Thomas T. Warner,Simon R. Hammans
Publsiher: Elsevier Health Sciences
Total Pages: 344
Release: 2008-11-04
ISBN 10: 0702038458
ISBN 13: 9780702038457
Language: EN, FR, DE, ES & NL

Practical Guide to Neurogenetics E Book Book Review:

This simple guide to neurogenetics demystifies the overwhelming amount of information on the subject so you can identify key clinical features and understand your management options. Reach relevant differential diagnoses and provide appropriate counseling to your patients using the symptom-based approach. By integrating genetic and neurological approaches to diagnoses, this book ensures that the neurological consequences of a genetic diagnosis and the genetic consequences of a neurological diagnosis are clear and explicit. Concise and portable, this book is ideal for easy reference in clinical use. Details the underlying basic science and clinical features of genetic disorders by taking a symptom-based approach to provide you with a comprehensive understanding of the field. Focuses on the clinical application of neurogenetics to be of practical use to you in the clinic. Clarifies the neurological consequences of a genetic diagnosis and the genetic consequences of a neurological diagnosis by integrating genetic and neurological approaches to diagnoses. Discusses and evaluates necessary investigations so you know when to use them and when to refer. Highlights diagnostic and therapeutic tips so you can learn new concepts or refine your skills in practice. Refers to online sources, such as Online Mendelian Inheritance in Man (OMIM) and others, to help you supplement your knowledge.

Human Genetics and Genomics

Human Genetics and Genomics
Author: Bahar Taneri,Esra Asilmaz,Türem Delikurt,Pembe Savas,Seniye Targen,Yagmur Esemen
Publsiher: John Wiley & Sons
Total Pages: 160
Release: 2020-06-02
ISBN 10: 3527337482
ISBN 13: 9783527337484
Language: EN, FR, DE, ES & NL

Human Genetics and Genomics Book Review:

Finally meeting the need for a laboratory manual on human genetics, this practical guide is the perfect companion title to all major standard textbooks on the subject. The authors all have a high-level research background and are actively involved in teaching and counseling. Based on a standard curriculum in human genetics, each chapter equals one practical unit of the course and topics range from basics in human inheritance to genetics in major disease clusters and from bioinformatics and personalized medicine to genetic counseling.

Neurogenetics

Neurogenetics
Author: Anonim
Publsiher: Elsevier
Total Pages: 436
Release: 2018-01-08
ISBN 10: 0444632352
ISBN 13: 9780444632357
Language: EN, FR, DE, ES & NL

Neurogenetics Book Review:

Genetic methodologies are having a significant impact on the study of neurological and psychiatric disorders. Using genetic science, researchers have identified over 200 genes that cause or contribute to neurological disorders. Still an evolving field of study, defining the relationship between genes and neurological and psychiatric disorders is evolving rapidly and expected to grow in scope as more disorders are linked to specific genetic markers. Part I covers basic genetic concepts and recurring biological themes, and begins the discussion of movement disorders and neurodevelopmental disorders, leading the way for Part II to cover a combination of neurological, neuromuscular, cerebrovascular, and psychiatric disorders. This volume in the Handbook of Clinical Neurology will provide a comprehensive introduction and reference on neurogenetics for the clinical practitioner and the research neurologist. Presents a comprehensive coverage of neurogenetics Details the latest science and impact on our understanding of neurological psychiatric disorders Provides a focused reference for clinical practitioners and the neuroscience/neurogenetics research community

Neurogenetics

Neurogenetics
Author: Nicholas Wood
Publsiher: Cambridge University Press
Total Pages: 241
Release: 2012-04-12
ISBN 10: 052154372X
ISBN 13: 9780521543729
Language: EN, FR, DE, ES & NL

Neurogenetics Book Review:

A coherent, up-to-date overview of the rapidly advancing field of neurogenetics for neurologists of any level.

Neurogenetics

Neurogenetics
Author: Stefan-M. Pulst
Publsiher: Contemporary Neurology
Total Pages: 458
Release: 2000
ISBN 10: 9780195129755
ISBN 13: 019512975X
Language: EN, FR, DE, ES & NL

Neurogenetics Book Review:

Neurogenetics is intended for any physician or scientist who manages patients with inherited diseases of the nervous system. It presents the clinical phenotypes of the most commonly inherited neurologic diseases, and their molecular pathogenesis, followed by a description of the appropriate tests to be used in diagnosis. Two introductory chapters familiarize the nongeneticist with medical genetic terminology and molecular genetic techniques useful in the analysis of genetic disease and genetic testing. Subsequent chapters examine major neurologic disorders caused by single defects, as well as disease phenotypes such as Alzheimer disease or amyotrophic lateral sclerosis which may be caused by defects in single genes, but may also be seen as sporadic diseases. The genetic components of other common neurologic disorders, such as epilepsy, multiple sclerosis, migraine, and stroke are all covered in detail. The final chapter discusses genetic counseling of symptomatic and pre-symptomatic individuals. Throughout, chapters discuss genotype/phenotype correlations and, where appropriate, animal models for inherited human neurologic diseases. Several chapters are devoted to recently discovered diseases caused by unstable DNA repeats. Special emphasis is placed on conveying how DNA testing can be applied to the daily practice of geneticists and neurologists.

Oxford Desk Reference Clinical Genetics and Genomics

Oxford Desk Reference  Clinical Genetics and Genomics
Author: Helen V. Firth,Jane A. Hurst
Publsiher: Oxford University Press
Total Pages: 824
Release: 2017-09-08
ISBN 10: 0192519824
ISBN 13: 9780192519825
Language: EN, FR, DE, ES & NL

Oxford Desk Reference Clinical Genetics and Genomics Book Review:

A popular and easy-to-use guide, this book is a must-have tool for clinical consultations in genetics and genomic medicine. Ideal for quick reference during practice, it covers the process of diagnosis, investigation, management, and counselling for patients. With a strong evidence base and international guidelines, it puts reliable and trustworthy guidance at your fingertips. Designed for use as a first-line guide, the A to Z format ensures it's accessible, and the simple layout makes it easy to assimilate information. Highly illustrated, the book also contains up-to-date glossaries of terms used in genetics and dysmorphology providing quick reference for key concepts. The second edition is an eagerly anticipated update of the gold standard in the specialty. It covers new developments in the field, particularly the advent of genome-wide sequencing and major updates in cancer. Fifteen new topics have been added, including Sudden cardiac death, Neonatal screening, and Ciliopathies. The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both outpatient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered, and where available diagnostic criteria are included. In addition there are chapters on familial cancer and pregnancy-related topics such as fetal anomalies, teratogens, prenatal and pre-implantation diagnosis and non-invasive prenatal testing. The book also provides information on the less common situations where management is particularly complex. Both practical and pertinent, Oxford Desk Reference: Clinical Genetics and Genomics is the companion you need by your side during clinical consultations.

Neurodegeneration

Neurodegeneration
Author: Anthony Schapira,Zbigniew K. Wszolek,Ted M. Dawson,Nicholas Wood
Publsiher: John Wiley & Sons
Total Pages: 344
Release: 2017-02-08
ISBN 10: 1118661923
ISBN 13: 9781118661925
Language: EN, FR, DE, ES & NL

Neurodegeneration Book Review:

This book unites the diverse range of complex neurodegenerative diseases into a textbook designed for clinical practice, edited by globally leading authorities on the subject. Presents a clinically oriented guide to the diseases caused by neurodegeneration Templated chapters combine clinical and research information on neurodegenerative diseases beginning with the common elements before treating each disease individually Diseases are grouped by anatomical regions of degeneration and include common disorders such as Parkinson’s Disease, Alzheimer’s Disease, Amyotrophic Lateral Sclerosis/Motor Neuron Disease, and Multiple Sclerosis as well as less common diseases Edited by globally leading authorities on the subject, and written by expert contributing authors

Neurogenetics

Neurogenetics
Author: Roger N. Rosenberg
Publsiher: Lippincott Williams & Wilkins
Total Pages: 324
Release: 1986
ISBN 10: 1928374650XXX
ISBN 13: UOM:39015009581185
Language: EN, FR, DE, ES & NL

Neurogenetics Book Review:

Neurogenetics in Neurology From Molecular Neuroscience to Precision Medicine

Neurogenetics in Neurology  From Molecular Neuroscience to Precision Medicine
Author: Matthew James Farrer,Guy Rouleau
Publsiher: Frontiers Media SA
Total Pages: 135
Release: 2020-12-22
ISBN 10: 2889662519
ISBN 13: 9782889662517
Language: EN, FR, DE, ES & NL

Neurogenetics in Neurology From Molecular Neuroscience to Precision Medicine Book Review:

The Practical Guide to the Genetic Family History

The Practical Guide to the Genetic Family History
Author: Robin L. Bennett
Publsiher: John Wiley & Sons
Total Pages: 384
Release: 2011-09-20
ISBN 10: 1118209818
ISBN 13: 9781118209813
Language: EN, FR, DE, ES & NL

The Practical Guide to the Genetic Family History Book Review:

HELPS YOU DEVELOP AND ASSESS PEDIGREES TO MAKE DIAGNOSES, EVALUATE RISK, AND COUNSEL PATIENTS The Second Edition of The Practical Guide to the Genetic Family History not only shows how to take a medical-family history and record a pedigree, but also explains why each bit of information gathered is important. It provides essential support in diagnosing conditions with a genetic component. Moreover, it aids in recommending genetic testing, referring patients for genetic counseling, determining patterns of inheritance, calculating risk of disease, making decisions for medical management and surveillance, and informing and educating patients. Based on the author's twenty-five years as a genetic counselor, the book also helps readers deal with the psychological, social, cultural, and ethical problems that arise in gathering a medical-family history and sharing findings with patients. Featuring a new Foreword by Arno Motulsky, widely recognized as the founder of medical genetics, and completely updated to reflect the most recent findings in genetic medicine, this Second Edition presents the latest information and methods for preparing and assessing a pedigree, including: Value and utility of a thorough medical-family history Directed questions to ask when developing a medical-family history for specific disease conditions Use of pedigrees to identify individuals with an increased susceptibility to cancer Verification of family medical information Special considerations when adoptions or gamete donors are involved Ethical issues that may arise in recording a pedigree Throughout the book, clinical examples based on hypothetical families illustrate key concepts, helping readers understand how real issues present themselves and how they can be resolved. This book will enable all healthcare providers, including physicians, nurses, medical social workers, and physician assistants, as well as genetic counselors, to take full advantage of the pedigree as a primary tool for making a genetic risk assessment and providing counseling for patients and their families.

A Practical Guide to Human Cancer Genetics

A Practical Guide to Human Cancer Genetics
Author: Shirley V. Hodgson,William D. Foulkes,Charis Eng,Eamonn R. Maher
Publsiher: Springer Science & Business Media
Total Pages: 420
Release: 2013-11-22
ISBN 10: 1447123751
ISBN 13: 9781447123750
Language: EN, FR, DE, ES & NL

A Practical Guide to Human Cancer Genetics Book Review:

This is a comprehensive and up-to-date guide to the diagnosis, clinical features and management of inherited disorders conferring cancer susceptibility. It is fully updated with much molecular, screening and management information. It covers risk analysis and genetic counselling for individuals with a family history of cancer. It also discusses predictive testing and the organisation of the cancer genetics service. There is information about the genes causing Mendelian cancer predisposing conditions and their mechanism of action. It aims to provide such details in a practical format for geneticists and clinicians in all disciplines.

Emery and Rimoin s Principles and Practice of Medical Genetics and Genomics

Emery and Rimoin   s Principles and Practice of Medical Genetics and Genomics
Author: Reed E. Pyeritz,Bruce R. Korf,Wayne W. Grody
Publsiher: Academic Press
Total Pages: 318
Release: 2021-11-02
ISBN 10: 0128152370
ISBN 13: 9780128152379
Language: EN, FR, DE, ES & NL

Emery and Rimoin s Principles and Practice of Medical Genetics and Genomics Book Review:

Emery and Rimoin’s Principles and Practice of Medical Genetics and Genomics: Perinatal and Reproductive Genetics, Seventh Edition includes the latest information on seminal topics such as prenatal diagnosis, genome and exome sequencing, public health genetics, genetic counseling, and management and treatment strategies in this growing field. The book is ideal for medical students, residents, physicians and researchers involved in the care of patients with genetic conditions. This comprehensive, yet practical resource emphasizes theory and research fundamentals related to applications of medical genetics across the full spectrum of inherited disorders and applications to medicine more broadly. Chapters from leading international researchers and clinicians focus on topics ranging from single gene testing to whole genome sequencing, whole exome sequencing, gene therapy, genome editing approaches, FDA regulations on genomic testing and therapeutics, and ethical aspects of employing genomic technologies. Fully revised and up-to-date, this new edition introduces genetic researchers, students and healthcare professionals to genomic technologies, testing and therapeutic applications Examines key topics and developing methods within genomic testing and therapeutics, including single gene testing, whole genome and whole exome sequencing, gene therapy and genome editing, variant Interpretation and classification, and ethical aspects of applying genomic technologies Includes color images that support the identification, concept illustration, and method of processing Features contributions by leading international researchers and practitioners of medical genetics Provides a robust companion website that offers further teaching tools and links to outside resources and articles to stay up-to-date on the latest developments in the field

Enjoy Your Science Meeting A Practical Guide To Getting The Most Out Of Attending Scientific Conferences

Enjoy Your Science Meeting   A Practical Guide To Getting The Most Out Of Attending Scientific Conferences
Author: Elizabeth M Fisher,Richard C Thompson
Publsiher: World Scientific
Total Pages: 168
Release: 2019-09-16
ISBN 10: 1786347245
ISBN 13: 9781786347244
Language: EN, FR, DE, ES & NL

Enjoy Your Science Meeting A Practical Guide To Getting The Most Out Of Attending Scientific Conferences Book Review:

The book provides a practical and readable guide to getting the most out of attending a scientific conference. The topics covered include writing an abstract, preparing and presenting a poster or talk, chairing a session, making good use of poster and oral sessions, and networking. Also included is practical advice on registering for a conference and planning travel. Aimed primarily at PhD students who are attending their first conference, it is also relevant to junior postdoctoral scientists.Different types of scientific conferences are discussed, together with their distinct roles in the development of a scientific career. After reading this book, a student or postdoc will be in a better position to make an effective presentation of their work at a conference and to achieve the maximum benefit from attending the conference, including promoting their work, learning about the latest developments and getting to know the key players in their field.

Practical Guide in Andrology and Embryology

Practical Guide in Andrology and Embryology
Author: Gita Ganguly Mukherjee,Gautam Khastgir,Ratna Chattopadhyay
Publsiher: Jaypee Brothers Medical Publishers
Total Pages: 436
Release: 2018-04-30
ISBN 10: 9352704851
ISBN 13: 9789352704859
Language: EN, FR, DE, ES & NL

Practical Guide in Andrology and Embryology Book Review:

Part of a new series on reproductive medicine, this book is a complete guide to andrology and embryology. Divided into 38 chapters, the text begins with in depth discussion on male infertility covering sperm function tests, screening, sperm selection for ART, sperm banking, and various causes of male infertility. The second part of the book examines assisted reproductive techniques in male infertility, frozen embryo transfer, oocyte and embryo cryopreservation, third party reproduction, and more. The book presents the latest advances in the field and each chapter includes key points and references for further reading. Clinical photographs, diagrams and tables further enhance the comprehensive text. Other titles in the series include: Practical Guide in Infertility, Practical Guide in Reproductive Surgery and Practical Guide in Assisted Reproductive Technology. Key points Comprehensive guide to andrology and embryology Part of new series on reproductive medicine Covers numerous ART procedures for male infertility Chapters include key points and detailed references for further reading

Practical Neurology

Practical Neurology
Author: Biller
Publsiher: Lippincott Williams & Wilkins
Total Pages: 747
Release: 2012
ISBN 10: 1451142633
ISBN 13: 9781451142631
Language: EN, FR, DE, ES & NL

Practical Neurology Book Review:

This book is a practical, concise alternative to existing neurology textbooks. The outline format and standard chapter template offers the reader immediate, comprehensive information. The author is a well-respected educator who has a talent for making neurologic information accessible and understandable. Significant changes have been made to the therapeutics/management portion of the book as well as specific diagnosis-related chapters have been updated. More tables and figures allow the reader to find the information quickly. This book sits between a handbook and a textbook and distinguishes itself in its presentation of material in a problem-oriented format: 35 chapters discuss how to approach the patient with a variety of disorders; the second half of the book discusses treatment options.

Clinical Neurogenetics An Issue of Neurologic Clinics

Clinical Neurogenetics  An Issue of Neurologic Clinics
Author: Brent L. Fogel
Publsiher: Elsevier Health Sciences
Total Pages: 281
Release: 2013-11-06
ISBN 10: 0323261094
ISBN 13: 9780323261098
Language: EN, FR, DE, ES & NL

Clinical Neurogenetics An Issue of Neurologic Clinics Book Review:

This issue of Neurologic Clinics features a review of clinical neurogenetics as it pertains to the following disorders: Huntington Disease; Autism/ASD;Fragile X Tremor Ataxia Syndrome (FXTAS); Lysosomal Storage Diseases; Psychiatric Disorders; Dominant Spinocerebellar Ataxias; Metabolic Disorders; Friedreich Ataxia; ALS; Dementia; Neuromuscular Disorders; Stroke; Epilepsy; and Dystonia.

Neurogenetic Developmental Disorders

Neurogenetic Developmental Disorders
Author: Michèle M. M. Mazzocco,Judith L. Ross
Publsiher: MIT Press
Total Pages: 507
Release: 2007
ISBN 10: 0262134802
ISBN 13: 9780262134804
Language: EN, FR, DE, ES & NL

Neurogenetic Developmental Disorders Book Review:

A reference to guide clinicians, researchers, teachers, and parents in identifying arange of genetic disorders despite widely variable cognitive, behavioral, and physicaleffects.

Rosenberg s Molecular and Genetic Basis of Neurological and Psychiatric Disease

Rosenberg s Molecular and Genetic Basis of Neurological and Psychiatric Disease
Author: Roger N. Rosenberg,Juan M. Pascual
Publsiher: Elsevier
Total Pages: 1464
Release: 2014-10-28
ISBN 10: 0124105491
ISBN 13: 9780124105492
Language: EN, FR, DE, ES & NL

Rosenberg s Molecular and Genetic Basis of Neurological and Psychiatric Disease Book Review:

Rosenberg’s Molecular and Genetic Basis of Neurologic and Psychiatric Disease, Fifth Edition provides a comprehensive introduction and reference to the foundations and key practical aspects relevant to the majority of neurologic and psychiatric disease. A favorite of over three generations of students, clinicians and scholars, this new edition retains and expands the informative, concise and critical tone of the first edition. This is an essential reference for general medical practitioners, neurologists, psychiatrists, geneticists, and related professionals, and for the neuroscience and neurology research community. The content covers all aspects essential to the practice of neurogenetics to inform clinical diagnosis, treatment and genetic counseling. Every chapter has been thoroughly revised or newly commissioned to reflect the latest scientific and medical advances by an international team of leading scientists and clinicians. The contents have been expanded to include disorders for which a genetic basis has been recently identified, together with abundant original illustrations that convey and clarify the key points of the text in an attractive, didactic format. Previous editions have established this book as the leading tutorial reference on neurogenetics. Researchers will find great value in the coverage of genomics, animal models and diagnostic methods along with a better understanding of the clinical implications. Clinicians will rely on the coverage of the basic science of neurogenetics and the methods for evaluating patients with biochemical abnormalities or gene mutations, including links to genetic testing for specific diseases. Comprehensive coverage of the neurogenetic foundation of neurological and psychiatric disease Detailed introduction to both clinical and basic research implications of molecular and genetic understanding of the brain Detailed coverage of genomics, animal models and diagnostic methods with new coverage of evaluating patients with biochemical abnormalities or gene mutations

Our Genes Our Choices

Our Genes  Our Choices
Author: David Goldman
Publsiher: Academic Press
Total Pages: 272
Release: 2012-05-18
ISBN 10: 9780123969521
ISBN 13: 0123969522
Language: EN, FR, DE, ES & NL

Our Genes Our Choices Book Review:

Our Genes, Our Choices: How Genotype and Gene Interactions Affect Behavior - First Prize winner of the 2013 BMA Medical Book Award for Basic and Clinical Sciences - explains how the complexity of human behavior, including concepts of free will, derives from a relatively small number of genes, which direct neurodevelopmental sequence. Are people free to make choices, or do genes determine behavior? Paradoxically, the answer to both questions is "yes," because of neurogenetic individuality, a new theory with profound implications. Author David Goldman uses judicial, political, medical, and ethical examples to illustrate that this lifelong process is guided by individual genotype, molecular and physiologic principles, as well as by randomness and environmental exposures, a combination of factors that we choose and do not choose. Written in an authoritative yet accessible style, the book includes practical descriptions of the function of DNA, discusses the scientific and historical bases of genethics, and introduces topics of epigenetics and the predictive power of behavioral genetics. First Prize winner of the 2013 BMA Medical Book Award for Basic and Clinical Sciences Poses and resolves challenges to moral responsibility raised by modern genetics and neuroscience Analyzes the neurogenetic origins of human behavior and free will Written by one of the world's most influential neurogeneticists, founder of the Laboratory of Neurogenetics at the National Institutes of Health

Cognitive and Communication Interventions

Cognitive and Communication Interventions
Author: Martha S. Burns
Publsiher: Plural Publishing
Total Pages: 318
Release: 2020-10-12
ISBN 10: 1635506662
ISBN 13: 9781635506662
Language: EN, FR, DE, ES & NL

Cognitive and Communication Interventions Book Review:

Understanding the recent science about how therapy changes the brain can empower clinicians to face the challenges of increasingly demanding medical and educational settings. However, many speech-language pathologists (SLPs) are unaware of the vast impact new neuroscience research has on clinical practice. Cognitive and Communication Interventions: Neuroscience Applications for Speech-Language Pathologists is a practical guide that informs and enables SLP’s, clinical psychologists, and other therapeutic professionals to use new research to enhance their clinical outcomes. Although based on independent neuroscience principles and research, this unique book is designed to be a readable and scientifically sound clinical guidebook. Written with the busy clinician in mind, this professional resource uses accessible, easy-to-understand language to walk readers through the complexities of neuroscience and provide workable strategies for application. The beginning chapters break down important concepts, such as neuroplasticity, environmental stressors, and connectomics, to create a base of understanding. The middle chapters delve into recent investigations of factors that potentially affect typical brain development, as well as disrupt connectomics. The final chapters provide neuroscience considerations for intervention, including the “What, How, and When” of therapy and other important considerations for individualizing and maximizing outcomes. Throughout the book, clinicians will also find case studies that provide examples of the practical applications of neuroscience research and study questions to improve memory and inference.