Petrides p e (36 Ergebnisse)

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Zustand: New. Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently ver.

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the worldhave contributed to this volume, the first of its kind to put together the current knowledge. The book deals with the new WHO classification of these disorders, novel aspects of diagnostic pathology, the search for disease-relevant genes utilizing molecular biology and proteomic techniques, the description of the roles of PVR-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included.…

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the worldhave contributed to this volume, the first of its kind to put together the current knowledge. The book deals with the new WHO classification of these disorders, novel aspects of diagnostic pathology, the search for disease-relevant genes utilizing molecular biology and proteomic techniques, the description of the roles of PVR-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included.…

Buch. Zustand: Neu. Molecular Basis of Chronic Myeloproliferative Disorders | P. E. Petrides | Buch | xii | Englisch | 2004 | Springer Berlin Heidelberg | EAN 9783540224853 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

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Zustand: gut. Molecular Basis of Chronic Myeloproliferative Disorders In deutscher Sprache. pages.

32. Zustand: Wie neu. 6., korr. Aufl. 1998. 1155 S., 1130 überwiegend farb. Einzelabb., 233 Tab., 27 x 19 cm, gebunden Dieses umfassende Standardwerk für die Biochemie und Pathobiochemie ist inhaltlich speziell auf die Bedürfnisse des Medizinstudenten abgestimmt. Didaktik vom Feinsten. Topaktuell und ideal zum Nachschlagen. In kürzester Zeit hat es sich seinen Spitzenpla Sprache: Deutsch.…

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Softcover/Taschenbuch. Zustand: Neu. 1. Wasser und Bioelemente.- 2. Kohlenhydrate.- 3. Lipide.- 4. Nucleotide und Polynucleotide (Nucleins?uren).- 5. Aminos?uren und Polyaminos?uren (Proteine).- 6. Cellul?re Organellen und Strukturen.- 7. Biokatalyse.- 8. Stoffwechsel und Funktion der Nucleins?uren.- 9. Mechanismus und Regulation der Proteinbiosynthese.- 10. Viren.- 11. Genetisch bedingte Proteindefekte.- 12. Bioenergetik.- 13. Grundlagen des Intermedi?rstoffwechsels.- 14. Intermedi?rstoffwechsel I: Citratcyclus.- 15. Intermedi?rstoffwechsel II: Kohlenhydrate.- 16. Intermedi?rstoffwechsel III: Lipide.- 17. Intermedi?rstoffwechsel IV: Aminos?uren.- 18. Intermedi?rstoffwechsel V: Purine und Pyrimidine.- 19. Intermedi?rstoffwechsel VI: H?m und Gallenfarbstoffe.- 20. Wasser- und Elektrolythaushalt.- 21. Spurenelemente.- 22. Vitamine.- 23. Ern?hrung.- 24. Endokrine Gewebe I: Allgemeine Grundlagen.- 25. Endokrine Gewebe II: Die schnelle Stoffwechselregulation.- 26. Endokrine Gewebe III: Hypothalamisch-hypophys?res System und Zielgewebe.- 27. Endokrine Gewebe IV: Regulation des Wasser- und Elektrolythaushalts.- 28. Gastrointestinaltrakt.- 29. Leber.- 30. Blut.- 31. Muskelgewebe.- 32. Binde- und St?tzgewebe.- 33. Nervengewebe.- 34. Immunsystem.- 35. Nieren und Urin.- 36. Tumorgewebe.- 1. Hinweisindex zum Gegenstandskatalog "Chemie f?r Mediziner und Biochemie".- 2. Hinweisindex zum Gegenstandskatalog "Pathophysiologie/Pathobiochemie". De Gewicht in Gramm: 2511.…

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Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the worldhave contributed to this volume, the first of its kind to put together the current knowledge. The book deals with the new WHO classification of these disorders, novel aspects of diagnostic pathology, the search for disease-relevant genes utilizing molecular biology and proteomic techniques, the description of the roles of PVR-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included. 236 pp. Englisch.…

Buch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the worldhave contributed to this volume, the first of its kind to put together the current knowledge. The book deals with the new WHO classification of these disorders, novel aspects of diagnostic pathology, the search for disease-relevant genes utilizing molecular biology and proteomic techniques, the description of the roles of PVR-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included. 236 pp. Englisch.…

Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently ver.…

Buch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Since the first description of Philadelphia chromosome-negative chronic myeloproliferative disorders more than 100 years ago, the diagnosis and therapy of these conditions have been based primarily on clinical experience and judgement. Until recently very little was known about the molecular basis of these diseases. In order to spark research in this area basic scientists and clinicians from various parts of the world have contributed to this volume, the first of its kind to put together the current knowledge. The book deals with the new WHO classification of these disorders, novel aspects of diagnostic pathology, the search for disease-relevant genes utilizing molecular biology and proteomic techniques, the description of the roles of PVR-1 and VHL genes for polycythemias and the discovery of the gene mutation responsible for the idiopathic hypereosinophilic syndrome. A chapter on anagrelide, an important novel drug for the treatment of primary thrombocythemia, is included.Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 236 pp. Englisch.…