Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Hypermethioninemia

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ISBN 13 :
Total Pages : 82 pages
Book Rating : 4.:/5 (1 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Hypermethioninemia by : Cyrille Ndikumukiza

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Hypermethioninemia written by Cyrille Ndikumukiza and published by . This book was released on 2017 with total page 82 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Citrullinemia Type 2

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ISBN 13 :
Total Pages : 84 pages
Book Rating : 4.:/5 (962 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Citrullinemia Type 2 by : Ahmad Alharbi

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Citrullinemia Type 2 written by Ahmad Alharbi and published by . This book was released on 2015 with total page 84 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Medium/short-chain L-3-OH Acyl-COA DH Deficiency

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ISBN 13 :
Total Pages : 96 pages
Book Rating : 4.:/5 (974 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Medium/short-chain L-3-OH Acyl-COA DH Deficiency by : Jungyoon Moon

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Medium/short-chain L-3-OH Acyl-COA DH Deficiency written by Jungyoon Moon and published by . This book was released on 2016 with total page 96 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Congenital Adrenal Hyperplasia

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ISBN 13 :
Total Pages : 56 pages
Book Rating : 4.:/5 (962 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Congenital Adrenal Hyperplasia by : Alhanoof Alnafesah

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Congenital Adrenal Hyperplasia written by Alhanoof Alnafesah and published by . This book was released on 2016 with total page 56 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Biotinidase Deficiency (BIOT)

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ISBN 13 :
Total Pages : 82 pages
Book Rating : 4.:/5 (13 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Biotinidase Deficiency (BIOT) by : Rana Kodeih

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Biotinidase Deficiency (BIOT) written by Rana Kodeih and published by . This book was released on 2018 with total page 82 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around the American College of Medical Genetics Recommendation for Newborn Screening for 2-methylbutyryl-CoA Dehydrogenase Deficiency

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ISBN 13 :
Total Pages : 66 pages
Book Rating : 4.:/5 (962 download)

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Book Synopsis Examining Uncertainty Around the American College of Medical Genetics Recommendation for Newborn Screening for 2-methylbutyryl-CoA Dehydrogenase Deficiency by : Razan Algatan

Download or read book Examining Uncertainty Around the American College of Medical Genetics Recommendation for Newborn Screening for 2-methylbutyryl-CoA Dehydrogenase Deficiency written by Razan Algatan and published by . This book was released on 2016 with total page 66 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Variant Hemoglobinopathies (including HBE)

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ISBN 13 :
Total Pages : 80 pages
Book Rating : 4.:/5 (1 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Variant Hemoglobinopathies (including HBE) by : Mohammed Alsubaii

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Variant Hemoglobinopathies (including HBE) written by Mohammed Alsubaii and published by . This book was released on 2017 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Galactose Epimerase Deficiency

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ISBN 13 :
Total Pages : 98 pages
Book Rating : 4.:/5 (962 download)

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Book Synopsis Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Galactose Epimerase Deficiency by : Bsmah Bajan

Download or read book Examining Uncertainty Around American College of Medical Genetics Recommendations for Newborn Screening for Galactose Epimerase Deficiency written by Bsmah Bajan and published by . This book was released on 2016 with total page 98 pages. Available in PDF, EPUB and Kindle. Book excerpt:

WIC Nutrition Risk Criteria

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Publisher : National Academies Press
ISBN 13 : 0309053854
Total Pages : 392 pages
Book Rating : 4.3/5 (9 download)

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Book Synopsis WIC Nutrition Risk Criteria by : Institute of Medicine

Download or read book WIC Nutrition Risk Criteria written by Institute of Medicine and published by National Academies Press. This book was released on 1996-06-10 with total page 392 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book reviews the scientific basis for nutrition risk criteria used to establish eligibility for participation in the U.S. Department of Agriculture's Special Supplemental Nutrition Program for Women, Infants, and Children (WIC). The volume also examines the specific segments of the WIC population at risk for each criterion, identifies gaps in the scientific knowledge base, formulates recommendations regarding appropriate criteria, and where applicable, recommends values for determining who is at risk for each criterion. Recommendations for program action and research are made to strengthen the validity of nutrition risk criteria used in the WIC program.

Laboratory Guide to the Methods in Biochemical Genetics

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Publisher : Springer Science & Business Media
ISBN 13 : 3540766987
Total Pages : 860 pages
Book Rating : 4.5/5 (47 download)

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Book Synopsis Laboratory Guide to the Methods in Biochemical Genetics by : Nenad Blau

Download or read book Laboratory Guide to the Methods in Biochemical Genetics written by Nenad Blau and published by Springer Science & Business Media. This book was released on 2008-05-31 with total page 860 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Nutrition Management of Inherited Metabolic Diseases

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Publisher : Springer
ISBN 13 : 3319146211
Total Pages : 363 pages
Book Rating : 4.3/5 (191 download)

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Book Synopsis Nutrition Management of Inherited Metabolic Diseases by : Laurie E. Bernstein

Download or read book Nutrition Management of Inherited Metabolic Diseases written by Laurie E. Bernstein and published by Springer. This book was released on 2015-06-03 with total page 363 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Homocysteine and Vascular Disease

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Publisher : Springer Science & Business Media
ISBN 13 : 9780792362487
Total Pages : 480 pages
Book Rating : 4.3/5 (624 download)

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Book Synopsis Homocysteine and Vascular Disease by : K. Robinson

Download or read book Homocysteine and Vascular Disease written by K. Robinson and published by Springer Science & Business Media. This book was released on 2000-04-30 with total page 480 pages. Available in PDF, EPUB and Kindle. Book excerpt: This state-of-the-art review provides an in-depth and critical summary of homocysteine from its molecular basis to clinical relevance and current clinical trials of folic acid and vitamin B6. Written by leading workers in the field, the book provides an authoritative, comprehensive and thoroughly up-to-date overview for scientists and clinicians and any others engaged in the field. It will also be useful to anyone involved in managing vascular patients or cardiac risk factors, as well as biochemists, pharmacologists, general physicians, cardiologists and clinical and basic researchers with an interest in preventive medicine.

Human Body Odor

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Publisher : Springer Science & Business Media
ISBN 13 : 4431669086
Total Pages : 298 pages
Book Rating : 4.4/5 (316 download)

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Book Synopsis Human Body Odor by : Masumi Inaba

Download or read book Human Body Odor written by Masumi Inaba and published by Springer Science & Business Media. This book was released on 2013-11-11 with total page 298 pages. Available in PDF, EPUB and Kindle. Book excerpt: Strong body odor is a condition for which, until now, there have been few treatment methods. The Japanese authors, encouraged by the willingness of Oriental patients to undergo radical treatment, have developed the subcutaneous tissue shaving method, which eliminates the condition in a very short period of time without ugly scarring. The book Human Body Odor not only introduces the completely new subcutaneous tissue shaving method, it also questions conventional theories on the hair cycle itself and throws a new hypothesis about the process of hair generation and regeneration into the scientific arena. This could even lead in the future to a formula for retarding hair loss! Developed over the past twenty years, the authors' new surgical method for the radical treatment of bromidrosis represents a landmark in cosmetic surgery and dermatology!

A Clinical Guide to Inherited Metabolic Diseases

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Publisher : Cambridge University Press
ISBN 13 : 1139447181
Total Pages : 360 pages
Book Rating : 4.1/5 (394 download)

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Book Synopsis A Clinical Guide to Inherited Metabolic Diseases by : Joe T. R. Clarke

Download or read book A Clinical Guide to Inherited Metabolic Diseases written by Joe T. R. Clarke and published by Cambridge University Press. This book was released on 2005-12-08 with total page 360 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Inherited Metabolic Diseases

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Publisher : Springer Science & Business Media
ISBN 13 : 3540747230
Total Pages : 380 pages
Book Rating : 4.5/5 (47 download)

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Book Synopsis Inherited Metabolic Diseases by : Georg F. Hoffmann

Download or read book Inherited Metabolic Diseases written by Georg F. Hoffmann and published by Springer Science & Business Media. This book was released on 2009-11-21 with total page 380 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Advances in Human Genetics

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Publisher : Plenum Publishing Corporation
ISBN 13 : 9780306396014
Total Pages : 352 pages
Book Rating : 4.3/5 (96 download)

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Book Synopsis Advances in Human Genetics by : Harry Harris

Download or read book Advances in Human Genetics written by Harry Harris and published by Plenum Publishing Corporation. This book was released on 1970 with total page 352 pages. Available in PDF, EPUB and Kindle. Book excerpt: From reviews of previous volumes in the series: 'Extremely valuable...thoroughly recommended.'-Annals of Human Genetics 'The most lucid and stimulating discussions of the topic to be found anywhere.'-American Scientist

Small Molecule Therapy for Genetic Disease

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Publisher : Cambridge University Press
ISBN 13 : 1139490761
Total Pages : pages
Book Rating : 4.1/5 (394 download)

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Book Synopsis Small Molecule Therapy for Genetic Disease by : Jess G. Thoene

Download or read book Small Molecule Therapy for Genetic Disease written by Jess G. Thoene and published by Cambridge University Press. This book was released on 2010-08-23 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Thoene summarises the substantial work that has been accomplished in the treatment of inborn errors of metabolism with simple molecules. This handbook will enable interested clinician scientists to rapidly survey the field, thus ascertaining what has been done as well as future directions for therapeutic research. Its important introductory chapters discuss the infrastructure of the field. The book closely analyses the cofactors used to augment the function of defective enzymes and the compounds that are able to utilise an alternative pathway in order to avoid the consequences of the metabolic block present in the patient. Among other therapies, the authors discuss the use of zinc and tetrathiomolybdate to treat Wilson's disease and the use of cysteamine to treat nephropathic cystinosis.