Human Pathobiochemistry (eBook, PDF)

From Clinical Studies to Molecular Mechanisms
Redaktion: Oohashi, Toshitaka; Otsuka, Fumio; Barber, Chad L.; Ramirez, Francesco; Tsukahara, Hirokazu

• Format: PDF

Produktbeschreibung

Examines numerous clinical cases to aid the study of diagnosis, therapy and basic biochemical mechanisms

Emphasizes the role and importance of 'bench-to-bedside' training of health care professionals.

Fully illustrated and presented as a step-by-step guide to enhance the readers' learning experience

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Produktdetails

• Verlag: Springer Nature Singapore
• Seitenzahl: 349
• Erscheinungstermin: 13. März 2019
• Englisch
• ISBN-13: 9789811329777
• Artikelnr.: 55462417

Autorenporträt

Toshitaka Oohashi, Ph.D., Professor of Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan Hirokazu Tsukahara, M.D., Ph.D., Professor of Department of Pediatrics, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan Francesco Ramirez, Ph.D., Professor of Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, New York, NY 10029, USA Chad Barber, Ph.D., Assistant Professor of Biology: California Lutheran University, Thousand Oaks, CA 91360, USA Fumio Otsuka, M.D., Ph.D., Professor of Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan

Inhaltsangabe

Part1. Metabolic Disorders.- 1. Citrin Deficiency.- 2. Aspartoacylase Deficiency (Canavan Disease, N-Acetylaspartic Aciduria).- 3. Prominent Insulin Resistance in Congenital Generalized Lipoatrophy.- 4. Fabry Disease.- 5. Familial Hypercholesterolemia.- 6. Gaucher Disease.- 7. Heme Oxygenase-1 Deficiency.- 8. The Homocystinurias.- 9. Hypophosphatasia.- 10. Phenylketonuria.- 11. Triglyceride Deposit Cardiomyovasculopathy.- 12. Urea Cycle Disorders.- 13. Wilson Disease.- Part2. Genetics.- 14. Achondroplasia.- 15. Acute Myeloid Leukemia: Mutations Blocking Differentiation Lead to Distinct Leukemic Subtypes.- 16. 1-Antitrypsin Deficiency.- 17. Hereditary Anticoagulant Deficiencies.- 18. Cherubism.- 19. Cancer and Excess Iron.- 20. Fukuyama Congenital Muscular Dystrophy and Related Diseases.- 21. Hereditary Proteinuric Glomerular Disorders.- 22. Marfan Syndrome.- 23. When Materials Are at Fault: The Skeletal Collagens, Osteogenesis Imperfecta and Chondrodysplasias.- Part3. Others.- 24. Acute Kidney Injury: Transition to Chronic Kidney Disease.- 25. Type I Interferonopathies: Common Pathological Features Between Congenital Infections and Genetic Disorders.- 26. Epilepsy.- 27. Hemophagocytic Lymphohistiocytosis.- 28. Hepatitis C Virus Infection.- 29. Substance Abuse Emergencies.

Rezensionen

"I believe that the book will appeal more to clinicians, both young and experienced and to clinical researchers ... . The chapters are of reasonable and correct length and the language used is good and clear. The diagrams too are easy to follow. ... It can serve the doctors ... . a welcome addition to the ever growing publication list in biomedical sciences." (Venkatachalam Lakshminarayanan, goodreads.com, April 16, 2019)

"The book's emphasis is on its role and importance in 'bench-to-bedside' training of healthcare professionals with the hope that this approach will have wide appeal in many disciplines related to pathobiochemistry. ... This unique book combines biochemistry with molecular biology and presents various disorders in a case study format. This is indeed a unique strategy to present complex information. I am quite confident that medical students, researchers, clinicians and other healthcare professionals will find this book very useful." (Omer Iqbal, Doody's Book Reviews, 27 September, 2019)

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