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Inherited Metabolic Diseases: A Clinical Approach - Georg F. Hoffmann,William L. Nyhan,Johannes Zschocke,Georg F. (EDT) Hoffmann,Johannes (EDT) Zschocke
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Georg F. Hoffmann,William L. Nyhan,Johannes Zschocke,Georg F. (EDT) Hoffmann,Johannes (EDT) Zschocke:

Inherited Metabolic Diseases: A Clinical Approach - encadernado, livro de bolso

2010, ISBN: 3540747222

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Inherited Metabolic Diseases: A Clinical Approach Hoffmann, Georg F. Zschocke, Johannes and Nyhan, William L.:

Inherited Metabolic Diseases: A Clinical Approach Hoffmann, Georg F. Zschocke, Johannes and Nyhan, William L. - livro usado

ISBN: 9783540747222

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Georg F. Hoffmann,William L. Nyhan,Johannes Zschocke,Georg F. (EDT) Hoffmann,Johannes (EDT) Zschocke:
Inherited Metabolic Diseases: A Clinical Approach [With DVD ROM] - encadernado, livro de bolso

2010

ISBN: 9783540747222

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Hoffmann, Georg F. [Editor]; Zschocke, Johannes [Editor]; Nyhan, William L. [Editor];:
Inherited Metabolic Diseases: A Clinical Approach - encadernado, livro de bolso

2010, ISBN: 9783540747222

Springer, 2010-02-18. Hardcover. Good., Springer, 2010-02-18, 2.5

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Editor-Georg F. Hoffmann; Editor-Johannes Zschocke; Editor-William L. Nyhan:
Inherited Metabolic Diseases: A Clinical Approach - encadernado, livro de bolso

2010, ISBN: 9783540747222

Springer, 2010-02-18. Hardcover. Used: Good., Springer, 2010-02-18, 2.5

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Inherited Metabolic Diseases: A Clinical Approach

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. TOC:Introduction to Inborn Errors of Metabolism.- Disorders of Intermediary Metabolism.- Disorders of the Biosynthesis and Breakdown of Complex Molecules.- Neurotransmitter Defects and Related Disorders.- Other Inborn Errors of Metabolism.- Approach to the Patient with Metabolic Disease.- Pathological Neonatal Screening Results.- Metabolic Emergencies.- Cardiovascular Abnormalities.- Hepatic Abnormalities.- Gastrointestinal and General Abdominal Symptoms.- Renal and Electrolyte Disturbances.- Neurological Symptoms.- Myopathies.- Psychiatric Problems.- Eye Disorders.- Skin and Hair Disorders.- Sceletal Abnormalities.- Congenital Malformations.- Hematological Abnormalities.- Immunological Problems.- Peculiar Odour.- Investigations for Metabolic Disease.- Biochemical Studies.- Enzyme Studies.- DNA Studies.- Function Tests.- Other Investigations.- Postmodern Investigations.- Work-up for an Unclassified Multisystem Disease.- Work-up for a Possible Mitochondrial Disorder.- Indications for Lumbar Puncture.- Prenatal Diagnosis.- Family Analyses - Carrier Analysis.- Appendix.

Dados detalhados do livro - Inherited Metabolic Diseases: A Clinical Approach


EAN (ISBN-13): 9783540747222
ISBN (ISBN-10): 3540747222
Livro de capa dura
Ano de publicação: 2009
Editor/Editora: Springer
448 Páginas
Peso: 1,149 kg
Língua: eng/Englisch

Livro na base de dados desde 2008-06-03T20:41:43+01:00 (Lisbon)
Página de detalhes modificada pela última vez em 2024-02-28T09:54:21+00:00 (Lisbon)
Número ISBN/EAN: 9783540747222

Número ISBN - Ortografia alternativa:
3-540-74722-2, 978-3-540-74722-2
Ortografia alternativa e termos de pesquisa relacionados:
Autor do livro: zschocke, johannes hoffmann, williams, georg hoffmann, william hoffmann, kahler, johannes hoff, kähler, johannes uhl, hoffmann max, georg may
Título do livro: dvd, metabolic inherited disease, clinical and metabolic, metabolic inherited diseases


Dados da editora

Autor: Georg F. Hoffmann; Johannes Zschocke; William L. Nyhan
Título: Inherited Metabolic Diseases - A Clinical Approach
Editora: Springer; Springer Berlin
386 Páginas
Ano de publicação: 2009-12-18
Berlin; Heidelberg; DE
Impresso / Feito em
Língua: Inglês
123,04 € (DE)
126,49 € (AT)
153,65 CHF (CH)
Not available, publisher indicates OP

SA; Book with CD-ROM; Hardcover, Softcover / Medizin/Klinische Fächer; Pädiatrie; Verstehen; Medizin, Gesundheit; skin; differential diagnosis; management; biopsy; Inborn Errors of Metabolism; diagnosis; metabolic disease; care; screening; metabolism; metabolic disorder; medicine; prenatal diagnosis; treatment; DNA; Pediatrics; Medicine; B; Internal Medicine; General Practice / Family Medicine; Neurology; Pathology; Human Genetics; Klinische und Innere Medizin; Allgemeinmedizin / Familienmedizin; Neurologie und klinische Neurophysiologie; Pathologie; Genetik, Medizin; EA; DB; SA

to Inborn Errors of Metabolism.- Disorders of Intermediary Metabolism.- Disorders of the Biosynthesis and Breakdown of Complex Molecules.- Neurotransmitter Defects and Related Disorders.- Approach to the Patient with Metabolic Disease.- When to Suspect Metabolic Disease.- Metabolic Emergencies.- Metabolic Emergencies.- Metabolic Emergencies.- Metabolic Emergencies.- Metabolic Emergencies.- Metabolic Emergencies.- Metabolic Emergencies.- Metabolic Emergencies.- Patient Care and Treatment.- Anesthesia and Metabolic Disease.- Organ Systems in Metabolic Disease.- Approach to the Patient with Cardiovascular Disease.- Liver Disease.- Gastrointestinal and General Abdominal Symptoms.- Kidney Disease and Electrolyte Disturbances.- Neurological Disease.- Metabolic Myopathies.- Psychiatric Disease.- Eye Disorders.- Skin and Hair Disorders.- Physical Abnormalities in Metabolic Diseases.- Hematological Disorders.- Immunological Problems.- Investigations for Metabolic Diseases.- Newborn Screening for Inherited Metabolic Disease.- Biochemical Studies.- Enzymes, Metabolic Pathways, Flux Control Analysis, and the Enzymology of Specific Groups of Inherited Metabolic Diseases.- DNA Studies.- Pathology — Biopsy.- Suspected Mitochondrial Disorder.- Postmortem Investigations.- Function Tests.- Family Issues, Carrier Tests, and Prenatal Diagnosis.

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