Documents Diagnostics biologiques 4 résultats

- 1 ressource en ligne (xxx, 1478 pages) : illustrations (principalement en couleur)

Diagnostics biologiques ; Chimie clinique ; Diagnostics moléculaires - Technique ; Médecine - Laboratoires

'' Use THE definitive reference for laboratory medicine and clinical pathology! Tietz Textbook of Laboratory Medicine, 7th Edition provides the guidance necessary to select, perform, and evaluate the results of new and established laboratory tests. Comprehensive coverage includes the latest advances in topics such as clinical chemistry, genetic metabolic disorders, molecular diagnostics, hematology and coagulation, clinical microbiology, transfusion medicine, and clinical immunology. From a team of expert contributors led by Nader Rifai, this reference includes access to wide-ranging online resources on Expert Consult — featuring the comprehensive product with fully searchable text, regular content updates, animations, podcasts, over 1300 clinical case studies, lecture series, and more. " --Publisher

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- 1 ressource en ligne (xv, 1666 pages) : illustrations (principalement en couleur)

Diagnostics biologiques ; Médecine - Laboratoires - Technique

For more than 100 years, Henry's Clinical Diagnosis and Management by Laboratory Methods has been recognized as the premier text in clinical laboratory medicine, widely used by both clinical pathologists and laboratory technicians. Leading experts in each testing discipline clearly explain procedures and how they are used both to formulate clinical diagnoses and to plan patient medical care and long-term management. Employing a multidisciplinary approach, it provides cutting-edge coverage of automation, informatics, molecular diagnostics, proteomics, laboratory management, and quality control, emphasizing new testing methodologies throughout.

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- ix, 183 p.
Cote : QY 25 K95m 2009

Diagnostics biologiques

Ce document permet aux étudiants et aux professionnels soignants une consultation facile concernant les examens courants, et leur propose des réponses à certaines de leurs questions lors d'une demande d'analyse biologique

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- xx, 338 p. : ill.
Cote : WD 205 C641 2006

Maladies héréditaires métaboliques ; Diagnostics différentiels ; Diagnostics biologiques

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.

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