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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 a...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Hoffmann, Georg F. (Editor ), Zschocke, Johannes (Editor ), Nyhan, William L. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer, 2010.
Edición:1st ed. 2010.
Temas:
Acceso en línea:Texto Completo
Tabla de Contenidos:
  • 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.