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OverviewFull Product DetailsAuthor: Russell Saneto , Sumit Parikh , Bruce H. CohenPublisher: Elsevier Science Publishing Co Inc Imprint: Academic Press Inc Dimensions: Width: 15.20cm , Height: 2.30cm , Length: 22.90cm Weight: 0.730kg ISBN: 9780128008775ISBN 10: 0128008776 Pages: 338 Publication Date: 04 December 2015 Audience: Professional and scholarly , Professional & Vocational Format: Hardback Publisher's Status: Active Availability: Manufactured on demand  We will order this item for you from a manufactured on demand supplier. Table of Contents1. Clinical Correlates of Mitochondrial Physiology and Disease 2. MELAS-encoded diseases 3. MELAS-(classic presentation) 4. MERRF 5. Pearson Syndrome 6. Kearn-Sayre Syndrome 7. Chronic Progressive External Ophthalmoplegia 8. Leber Hereditary Optic Neuropathy 9. Leigh Syndrome 10. NARP 11. Maternal Inherited Diabetes 12. Sporadic Myopathy 13. Pyruvate Dehydrogenase Complex Deficiencies 14. Friedreich Ataxia 15. Leigh Syndrome 16. Reversible Myopathy 17. Childhood Alpers-Huttenlocher Syndrome 18. Juvenile Alpers-Huttenlocher Syndrome 19. Autosomal dominant Progressive External Ophthalmoplegia 20. c10orf2 (Twinkle) 21. MPV17/Deoxyguanosine Kinase 22. RRM2B 23. Mitochondrial Nasogastric Intestinal Encephalopathy 24. Thymidine Kinase 25. OPA1 26. MFN2 27. Aminoacyl-tRNA synthetase (CNS) 28. Aminoacyl-tRNA synthetase (Non-CNS) 29. MTO1 30. Complex I 31. Complex II 32. Complex III (GRACILE) 33. Complex IV 34. Complex V 35. Coenzyme Q10 (Primary Brain) 36. Coenzyme Q10 (Primary Renal)ReviewsAuthor InformationRussell P. Saneto is a pediatric neurologist who specializes in diagnosis and treatment of mitochondrial disorders and intractable epilepsy. His PhD was in human biochemical genetics was obtained at the University of Texas Medical Branch. His medical degree was obtained from the Des Moines University of Osteopathic Medicine and he did his pediatric, pediatric neurology, and pediatric neurophysiology fellowship at the Cleveland Clinic in Ohio. He began diagnosing and treatment of mitochondrial disease during residency and has continued studying this disorder during his career at Seattle Children's Hospital over the past 15 years. He is currently the Head of the Mitochondrial Medicine group at Seattle Children's and is a professor in the department of Neurology and adjunct Professor in Pediatrics. He has appointments in both Pediatrics and Neurology at Seattle Children's and University of Washington. Sumit Parikh, MD is the Director of the Cleveland Clinic Neurogenetics, Metabolic & Mitochondrial disease program. Dr. Parikh completed his residency in pediatrics and fellowship in child neurology at the Children's Hospital of Pittsburgh. He received additional training in genetics and metabolism at Cleveland Clinic and Centers for Inherited Diseases of Metabolism. Dr. Parikh is part of the North American Mitochondrial Disease Research Consortium (NAMDC) and the Primary Investigator for the Pearson Syndrome Natural History study. He serves as the current chair of the United Mitochondrial Disease Foundation Scientific & Medical Advisor Board. He is the immediate Past-President of the Mitochondrial Medicine Society. Tab Content 6Author Website:Countries AvailableAll regions |
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