A Quick Guide to Metabolic Disease Testing Interpretation

A Quick Guide to Metabolic Disease Testing Interpretation
Author: Patricia Jones,Khushbu Patel,Dinesh Rakheja
Publsiher: Academic Press
Total Pages: 220
Release: 2020-07-31
ISBN 10: 0128169273
ISBN 13: 9780128169278
Language: EN, FR, DE, ES & NL

A Quick Guide to Metabolic Disease Testing Interpretation Book Review:

Accurate interpretation of the organic acid chromatographs obtained from the gas chromatography/mass spectrometry requires a significant amount of practice. Pattern recognition is an important factor and a skill that is gained through time and effort. A Quick Guide to Metabolic Disease Testing Interpretation, Second Edition, provides these example chromatographs demonstrating specific disease-related metabolites for the inborn error of metabolism diagnosed via this method. One or more representative chromatographs from each of the common disorders is presented, with the important compounds noted on the chromatographs. This is a must-have for laboratory and medical professionals who interpret testing for the diagnosis and monitoring of IEM. Includes pathway diagrams and representative compound scans of important diagnostic compounds Provides illustrative chromatographs from selected disorders to aid in diagnosing common inborn errors of metabolism Highlights brief descriptions of the etiology and clinical presentation of each presented disorder

Quick Guide to Organic Acid Interpretation

Quick Guide to Organic Acid Interpretation
Author: Patricia M. Jones,Dinesh Rakheja
Publsiher: AACC Press
Total Pages: 147
Release: 2011
ISBN 10: 9781594251269
ISBN 13: 1594251266
Language: EN, FR, DE, ES & NL

Quick Guide to Organic Acid Interpretation Book Review:

A Clinical Guide to Inherited Metabolic Diseases

A Clinical Guide to Inherited Metabolic Diseases
Author: Joe T. R. Clarke
Publsiher: Cambridge University Press
Total Pages: 135
Release: 2005-12-08
ISBN 10: 1139447181
ISBN 13: 9781139447188
Language: EN, FR, DE, ES & NL

A Clinical Guide to Inherited Metabolic Diseases Book Review:

This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis. The book is organized into chapters according to the most prominent presenting problem of patients with inherited metabolic diseases: neurologic, hepatic, cardiac, metabolic acidosis, dysmorphism, and acute catastrophic illness in the newborn. It also includes chapters on general principles, laboratory investigation, neonatal screening, and the principles of treatment. This new edition includes much greater depth on mitochondrial disease and congenital disorders of glycosylation. The chapters on neurological syndrome and newborn screening are greatly expanded, as are those on laboratory investigation and treatment, to take account of the very latest technological developments.

Small Animal Clinical Diagnosis by Laboratory Methods E Book

Small Animal Clinical Diagnosis by Laboratory Methods   E Book
Author: Michael D. Willard,Harold Tvedten
Publsiher: Elsevier Health Sciences
Total Pages: 432
Release: 2011-12-23
ISBN 10: 1437706584
ISBN 13: 9781437706581
Language: EN, FR, DE, ES & NL

Small Animal Clinical Diagnosis by Laboratory Methods E Book Book Review:

A quick guide to appropriately selecting and interpreting laboratory tests, Small Animal Clinical Diagnosis by Laboratory Methods, 5th Edition helps you utilize your in-house lab or your specialty reference lab to efficiently make accurate diagnoses without running a plethora of unnecessary and low-yield tests. It provides answers to commonly asked questions relating to laboratory tests, and solutions to frequently encountered problems in small animal diagnosis. For easy reference, information is provided by clinical presentation and abnormalities, and includes hundreds of tables, boxes, key points, and algorithms. This edition, now in full color, is updated with the latest advances in laboratory testing methods and diagnostic problem solving. Written by noted educators Dr. Michael Willard and Dr. Harold Tvedten, this book may be used as an on-the-spot guide to specific problems or conditions as well as a reference for more detailed research on difficult cases. Concise discussions address laboratory approaches to various disorders, possible conclusions from various test results, artifacts and errors in diagnoses, and interpretations leading to various diagnoses. Hundreds of tables, boxes, algorithms, and key points offer at-a-glance information including cautions, common pitfalls, and helpful "pearls," and lead to proper differential and clinical diagnostic decision making. Note boxes identify key considerations in correlating clinical signs with test data for accurate diagnoses, highlight safety precautions, and offer helpful tips for sample preparation and interpretation. Chapters on laboratory diagnostic toxicology and therapeutic drug monitoring help in handling potentially fatal poisonings and other special situations. Expert editors and contributors provide clinical knowledge and successful diagnostic problem-solving solutions. A practical appendix lists referral laboratories that may be contacted for certain diseases, and reference values with the normal or expected range for coagulation, hematology, and more. Updated coverage integrates the newest advances in testing methods and diagnostic problem solving. Full-color photos and schematic drawings are placed adjacent to related text, and accurately depict diagnostic features on microscopic slide preparations as well as test procedures and techniques.

Physician s Guide to the Laboratory Diagnosis of Metabolic Diseases

Physician   s Guide to the Laboratory Diagnosis of Metabolic Diseases
Author: N. Blau,M. Duran,M.E. Blaskovics,K.M. Gibson
Publsiher: Springer Science & Business Media
Total Pages: 716
Release: 2012-12-06
ISBN 10: 364255878X
ISBN 13: 9783642558788
Language: EN, FR, DE, ES & NL

Physician s Guide to the Laboratory Diagnosis of Metabolic Diseases Book Review:

This second edition of The Physician's Guide provides paediatricians and other physicians with a unique aid to help them select the correct diagnosis from a bewildering array of complex clinical and laboratory data. Delay and mistakes in the diagnosis of inherited metabolic diseases may have devastating consequences. The guide, which includes a CD-ROM, describes 298 disorders which have been grouped into 35 chapters according to the type of condition. Within each group of disorders, chapters provide tables of pertinent clinical findings as well as reference and pathological values for crucial metabolites. Relevant metabolic pathways and diagnostic flow charts are included. There are three indices to make the book as user-friendly as possible.

Drug Metabolism and Pharmacokinetics Quick Guide

Drug Metabolism and Pharmacokinetics Quick Guide
Author: Siamak Cyrus Khojasteh,Harvey Wong,Cornelis E.C.A. Hop
Publsiher: Springer Science & Business Media
Total Pages: 214
Release: 2011-04-07
ISBN 10: 1441956298
ISBN 13: 9781441956293
Language: EN, FR, DE, ES & NL

Drug Metabolism and Pharmacokinetics Quick Guide Book Review:

Drug Metabolism and Pharmacokinetics Quick Guide covers a number of aspects of drug assessment at drug discovery and development stages, topics such as pharmacokinetics, absorption, metabolism, enzyme kinetics, drug transporters, drug interactions, drug-like properties, assays and in silico calculations. It covers key concepts, with useful tables on physiological parameters (eg. blood flow to organs in x-species, expression and localization of enzymes and transporters), chemical structure, nomenclature, and moieties leading to bioactivation (with examples). Overall it includes a number of key topics useful at the drug discovery stage, which would serve as a quick reference with several examples from the literature to illustrate the concept.

Nutrition Management of Inherited Metabolic Diseases

Nutrition Management of Inherited Metabolic Diseases
Author: Laurie E. Bernstein,Fran Rohr,Joanna R. Helm
Publsiher: Springer
Total Pages: 377
Release: 2015-06-03
ISBN 10: 3319146211
ISBN 13: 9783319146218
Language: EN, FR, DE, ES & NL

Nutrition Management of Inherited Metabolic Diseases Book Review:

This up-to-date reference on the nutrition management of inherited metabolic diseases (IMD) covers a wide range of these disorders, including phenylketonuria and other aminoacidopathies, organic acidemias, urea cycle disorders, fatty acid oxidation disorders, galactosemia and glycogen storage diseases. Guidance is also provided on laboratory evaluations and biochemical testing and monitoring. Topics such as newborn screening for IMD, as well as nutrition management during pregnancy and transplantation, are addressed. The book is based on 7 years of lectures delivered through Metabolic University – an interactive, didactic program designed to provide training to dietitians who work with individuals with IMD. This book provides the basic information required to manage nutrition care and is a resource for clinicians new to this complex field.

Inherited Metabolic Disease in Adults

Inherited Metabolic Disease in Adults
Author: Carla E. M. Hollak,Robin Lachmann
Publsiher: Oxford University Press
Total Pages: 626
Release: 2016
ISBN 10: 0199972133
ISBN 13: 9780199972135
Language: EN, FR, DE, ES & NL

Inherited Metabolic Disease in Adults Book Review:

As clinical management of inherited metabolic diseases (IMDs) has improved, more patients affected by these conditions are surviving into adulthood. This trend, coupled with the widespread recognition that IMDs can present differently and for the first time during adulthood, makes the need for a working knowledge of these diseases more important than ever. Inherited Metabolic Disease in Adults offers an authoritative clinical guide to the adult manifestations of these challenging and myriad conditions. These include both the classic pediatric-onset conditions and a number of new diseases that can manifest at any age. It is the first book to give a clear and concise overview of how this group of conditions affects adult patients, a that topic will become a growing imperative for physicians across primary and specialized care.

A Clinical Guide to Inherited Metabolic Diseases

A Clinical Guide to Inherited Metabolic Diseases
Author: Joe T. R. Clarke
Publsiher: Cambridge University Press
Total Pages: 289
Release: 2002-07-11
ISBN 10: 9780521890762
ISBN 13: 0521890764
Language: EN, FR, DE, ES & NL

A Clinical Guide to Inherited Metabolic Diseases Book Review:

This clinically organized, user-friendly, handbook is a guide to the recognition of inherited metabolic disease, and provides direction once diagnosis has been established. It is a well-illustrated text that presents biochemical and metabolic concepts in a clinically relevant context. The volume complements traditional textbooks which are organized biochemically, and serves as an entrance to the discipline, to help general physicians and advanced medical trainees to overcome the intimidation of dealing with metabolic problems. This new edition has been expanded to include substantially more information on mitochondrial diseases, new imaging techniques, and new techniques for screening and diagnosis.

Inherited Metabolic Disease in Adults

Inherited Metabolic Disease in Adults
Author: Carla E. M. Hollak,Robin Lachmann
Publsiher: Oxford University Press
Total Pages: 744
Release: 2016-07-19
ISBN 10: 0199972141
ISBN 13: 9780199972142
Language: EN, FR, DE, ES & NL

Inherited Metabolic Disease in Adults Book Review:

As clinical management of inherited metabolic diseases (IMDs) has improved, more patients affected by these conditions are surviving into adulthood. This trend, coupled with the widespread recognition that IMDs can present differently and for the first time during adulthood, makes the need for a working knowledge of these diseases more important than ever. Inherited Metabolic Disease in Adults offers an authoritative clinical guide to the adult manifestations of these challenging and myriad conditions. These include both the classic pediatric-onset conditions and a number of new diseases that can manifest at any age. It is the first book to give a clear and concise overview of how this group of conditions affects adult patients, a that topic will become a growing imperative for physicians across primary and specialized care.

Physician s Guide to the Diagnosis Treatment and Follow Up of Inherited Metabolic Diseases

Physician s Guide to the Diagnosis  Treatment  and Follow Up of Inherited Metabolic Diseases
Author: Nenad Blau,Marinus Duran,K Michael Gibson,Carlo Dionisi Vici
Publsiher: Springer
Total Pages: 867
Release: 2014-07-08
ISBN 10: 3642403379
ISBN 13: 9783642403378
Language: EN, FR, DE, ES & NL

Physician s Guide to the Diagnosis Treatment and Follow Up of Inherited Metabolic Diseases Book Review:

This book, combining and updating two previous editions, is a unique source of information on the diagnosis, treatment, and follow-up of metabolic diseases. The clinical and laboratory data characteristic of rare metabolic conditions can be bewildering for both clinicians and laboratory personnel. Reference laboratory data are scattered, and clinical descriptions may be obscure. The Physician’s Guide documents the features of more than five hundred conditions, grouped according to type of disorder, organ system affected (e.g. liver, kidney, etc) or phenotype (e.g. neurological, hepatic, etc). Relevant clinical findings are provided and pathological values for diagnostic metabolites highlighted. Guidance on appropriate biochemical genetic testing is provided. Established experimental therapeutic protocols are described, with recommendations on follow-up and monitoring. The authors are acknowledged experts, and the book will be a valuable desk reference for all who deal with inherited metabolic diseases.

Genetic Skin Disorders

Genetic Skin Disorders
Author: Virginia P. Sybert
Publsiher: Oxford University Press
Total Pages: 624
Release: 2017-01-13
ISBN 10: 0190276479
ISBN 13: 9780190276478
Language: EN, FR, DE, ES & NL

Genetic Skin Disorders Book Review:

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. Organized with the needs of busy clinicians in mind, it offers detailed clinical guidance on the signs, symptoms, mode of inheritance, recurrence risk, and diagnosis of over 300 skin disorders, all in an accessible, at-a-glance format. Annotated bibliographies highlight the most relevant and up-to-date medical literature. Newly compiled lists of support groups, both national and international, for patients and their families supplement the ample resources for medical professionals. Informed by the author's extensive clinical experience and suffused with a distinctive, witty voice, GENETIC SKIN DISORDERS is an ideal companion in the laboratory, clinic, or consulting room. FEATURES . Includes both disease-based chapters and an appendix of skin signs that simplifies differential diagnosis for specialists and general practitioners alike . More than 800 color photographs illustrate the full spectrum of hair, skin, and nail abnormalities . Updated to reflect current classification of inherited skin disorders and the molecular underpinnings of these conditions "

Pediatric Endocrinology Two Volume Set

Pediatric Endocrinology  Two Volume Set
Author: Fima Lifshitz
Publsiher: CRC Press
Total Pages: 1352
Release: 2006-12-26
ISBN 10: 1420042734
ISBN 13: 9781420042733
Language: EN, FR, DE, ES & NL

Pediatric Endocrinology Two Volume Set Book Review:

Celebrating more than twenty years as the single best source in the field, this Fifth Edition has now expanded into two cornerstone volumes with 53 fully inclusive chapters and 73 renowned contributors that comprehensively address every topic and trend relevant to the identification, diagnosis, and management of endocrine and endocrin

Introduction to Critical Care Nursing E Book

Introduction to Critical Care Nursing E Book
Author: Mary Lou Sole,Deborah Goldenberg Klein,Marthe J. Moseley
Publsiher: Elsevier Health Sciences
Total Pages: 664
Release: 2020-07-04
ISBN 10: 0323759661
ISBN 13: 9780323759663
Language: EN, FR, DE, ES & NL

Introduction to Critical Care Nursing E Book Book Review:

Start here to master the concepts, technology, and procedures of critical care nursing! Introduction to Critical Care Nursing, 8th Edition prepares you to provide safe, effective, patient-centered care in a variety of high-acuity, progressive, and critical care settings. Evidence-based coverage includes realistic case studies and incorporates the latest advances in critical care. Disorders are conveniently organized by body system or special situation, and nursing management chapters include quick-reference nursing care plans. This clear, concise textbook will help you develop the knowledge and clinical reasoning skills needed for success in today's highly complex critical care environments. Critical Reasoning Activities are included throughout the text, promoting development of clinical nursing judgment to help you prepare for the Next-Generation NCLEX-RN® Exam. Emphasis on QSEN competencies enables you to gain the knowledge, skills, and attitudes needed to provide safe, high-quality health care in a variety of high acuity, progressive, and critical care settings. Evidence-Based Practice boxes illustrate how research evidence is used to address problems in patient care and includes nursing implications plus AACN’s new system for Levels of Evidence: A, B, C, D, E, and M. Universal Collaborative Plan of Care for the Critically Ill Patient addresses key aspects of collaborative/interprofessional care that apply to virtually all critically ill patients. Individual Plans of Care prepare you for clinical practice by describing patient problems, patient outcomes, and nursing assessments and interventions with rationales. Case studies challenge you to apply concepts to the real world, testing your clinical nursing judgment by asking questions about patient-specific cases with lab results. Clinical Alerts highlight potential problems and concerns to improve patient safety and clinical care. Laboratory Alerts emphasize the importance of laboratory test results to critical care nursing. Medication tables show the actions/usages, indications, dosages/routes, side effects, and nursing implications of medications commonly used in critical care settings. Coverage of cardiac assistive devices includes the ECMO device for extracorporeal life support, as well as other small, portable, bedside cardiac-assistive devices. Hemodynamic monitoring content now emphasizes the noninvasive methods of hemodynamic monitoring that are becoming more prominent. Coverage of infection control addresses the QSEN safety competency and helps provide patient protection against the growing threat of drug-resistant infections. Nearly 300 full-color photographs and drawings visually clarify key concepts and equipment for better understanding of today’s complex critical care environment.

Endocrine and Metabolic Disorders

Endocrine and Metabolic Disorders
Author: Robert F. Dons,Frank H. Wians, Jr.
Publsiher: CRC Press
Total Pages: 639
Release: 2009-06-17
ISBN 10: 9781420079364
ISBN 13: 1420079360
Language: EN, FR, DE, ES & NL

Endocrine and Metabolic Disorders Book Review:

Bottom Line Information to Effectively Diagnose Disorders The diagnosis, management, and clinical testing associated with old, traditional, and new endocrine disorders have seen numerous advances during the past 10 years since the publication of the previous edition of this bestselling resource. Updating its classic predecessor in content and format, Endocrine and Metabolic Testing Manual, Fourth Edition provides an authoritative and comprehensive resource on the clinical, diagnostic, and laboratory testing for endocrine disorders. Presents Relevant ICD-9 Codes for All Procedures and Tests Written by two widely respected authorities with more than 60 years of combined experience in diagnostic endocrinology, this medical guide is organized by endocrine organ system into 12 chapters. All tests within each chapter provide accurate, brief, but adequate, information regarding indications for the test, the procedure for performing the test, instructions for how to interpret test results, suggestions for further reading, and useful ICD-9 diagnosis codes. The book is laden with tables, making the information easy to find and use. Enhanced Features of the Fourth Edition: Expanded Coverage: Includes most endocrine and metabolic disorders and the appropriate testing associated with their diagnoses Improved Organization: Uses a more standardized format for easier use Sample Calculations: Assists in calculating complex formulas with ease and accuracy Highly Informative Tables: Summarizes critical information in a reader-friendly format With detailed instruction on how to perform and interpret clinical test procedures, this practical reference is an essential resource for endocrinologists and pathologists. Newly designed and reformatted, the new edition enables quick access to complete and authoritative information about the diagnosis, screening, and management of traditional and emerging endocrine disorders.

Assessing Genetic Risks

Assessing Genetic Risks
Author: Institute of Medicine,Committee on Assessing Genetic Risks
Publsiher: National Academies Press
Total Pages: 352
Release: 1994-01-01
ISBN 10: 0309047986
ISBN 13: 9780309047982
Language: EN, FR, DE, ES & NL

Assessing Genetic Risks Book Review:

Raising hopes for disease treatment and prevention, but also the specter of discrimination and "designer genes," genetic testing is potentially one of the most socially explosive developments of our time. This book presents a current assessment of this rapidly evolving field, offering principles for actions and research and recommendations on key issues in genetic testing and screening. Advantages of early genetic knowledge are balanced with issues associated with such knowledge: availability of treatment, privacy and discrimination, personal decisionmaking, public health objectives, cost, and more. Among the important issues covered: Quality control in genetic testing. Appropriate roles for public agencies, private health practitioners, and laboratories. Value-neutral education and counseling for persons considering testing. Use of test results in insurance, employment, and other settings.

Inherited Metabolic Diseases

Inherited Metabolic Diseases
Author: Georg F. Hoffmann,Johannes Zschocke,William L. Nyhan
Publsiher: Springer Science & Business Media
Total Pages: 386
Release: 2009-11-21
ISBN 10: 3540747230
ISBN 13: 9783540747239
Language: EN, FR, DE, ES & NL

Inherited Metabolic Diseases Book Review:

The explosion of insights in the field of metabolic disease has shed new light on diagnostic as well as treatment options. ‘Inherited Metabolic Disease – A Clinical Approach’ is written with a reader-friendly consistent structure. It helps the reader to find the information in an easily accessible and rapid way when needed. Starting with an overview of the major groups of metabolic disorders it includes algorithms with questions and answers as well as numerous graphs, metabolic pathways, and an expanded index. Clinical and diagnostic details with a system and symptom based are given to facilitate an efficient and yet complete diagnostic work-up of individual patients. Further, it offers helpful advice for emergency situations, such as hypoglycemia, hyperammonemia, lactic acidosis or acute encephalopathy. Five different indices allow a quick but complete orientation for common important constellations. Last but not least, it has an appendix with a guide to rapid differential diagnosis of signs and symptoms and when not to suspect metabolic disease. It will help physicians to diagnose patients they may otherwise fail to diagnose and to reduce unnecessary referrals. For metabolic and genetic specialists especially the indices will be helpful as a quick look when being called for advice. It has all it needs to become a gold standard defining the clinical practice in this field.

Pediatric Hospital Medicine

Pediatric Hospital Medicine
Author: Ronald M. Perkin,Dale A. Newton,James D. Swift
Publsiher: Lippincott Williams & Wilkins
Total Pages: 924
Release: 2008
ISBN 10: 9780781770323
ISBN 13: 0781770327
Language: EN, FR, DE, ES & NL

Pediatric Hospital Medicine Book Review:

Now in its Second Edition, this text focuses exclusively on the management of hospitalized pediatric patients from admission to discharge. It is an excellent resource for residency programs, hospitalist fellowships, and continuing education for physicians whose practice includes the management of hospitalized newborns and children. Because pediatric hospital care is provided by a wide variety of healthcare professionals and in many different hospital settings, this text provides a framework for unified management and effective and efficient care. This edition includes new sections on emergency medicine and psychiatric hospitalization and expanded coverage of management of children with complex and chronic conditions.

Clinical Laboratory Medicine for Mental Health Professionals

Clinical Laboratory Medicine for Mental Health Professionals
Author: Sandra A. Jacobson
Publsiher: American Psychiatric Pub
Total Pages: 388
Release: 2016-12-19
ISBN 10: 1615371214
ISBN 13: 9781615371211
Language: EN, FR, DE, ES & NL

Clinical Laboratory Medicine for Mental Health Professionals Book Review:

A revised, abridged version of the seminal work, Laboratory Medicine in Psychiatry and Behavioral Science, Clinical Laboratory Medicine for Mental Health Professionals more directly address the needs of general psychiatrists and their mental health colleagues in clinical practice. Sections on laboratory tests, diseases and conditions, and psychotropic medications include alphabetically arranged entries, making it easy for busy clinicians to reference the updated information. For each laboratory test, the following information is provided: The type of test (e.g., blood, urine, etc.) An explanation of the test The test's relevance to psychiatry Patient preparation Medical and psychiatric indications for the test Numerical reference ranges Critical values for test results The potential meaning of abnormal results (e.g., factors that lead to increased or decreased levels) Interfering factors Cross-references to other tests or conditions Information on clinical diagnosis and laboratory testing is provided for diseases and conditions, and psychotropic medications are examined from both a screening and a monitoring standpoint. Extensively indexed, this guide also includes an appendix that features at-a-glance information on therapeutic and psychotropic levels, 10 rules for deciding whether an ECG is normal, and several figures covering topics relevant to tests, such as ECG waves and intervals, cholestatic injury, bilirubin cycle, and SIADH secretion. Years of clinical practice and research inform both the choice of tests included and the rationale for their use, making Clinical Laboratory Medicine for Mental Health Professionals the definitive, authoritative reference for psychiatrists and other behavioral health clinicians.

Laboratory Guide to the Methods in Biochemical Genetics

Laboratory Guide to the Methods in Biochemical Genetics
Author: Nenad Blau,Marinus Duran,K. Michael Gibson
Publsiher: Springer Science & Business Media
Total Pages: 860
Release: 2008-05-31
ISBN 10: 3540766987
ISBN 13: 9783540766988
Language: EN, FR, DE, ES & NL

Laboratory Guide to the Methods in Biochemical Genetics Book Review:

This manual deals specifically with laboratory approaches to diagnosing inborn errors of metabolism. The key feature is that each chapter is sufficiently detailed so that any individual can adopt the described method into their own respective laboratory.