P e petrides (33 risultati)

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Condizione: Used. pp. 236.

Condizione: Used. pp. 236.

Condizione: Used. pp. 236.

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Condizione: New. In English.

Buch. Condizione: 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. Condizione: 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.…

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

32. Condizione: 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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Condizione: New. pp. 1036 4. Aufl. 1988 edition NO-PA16APR2015-KAP.

Paperback. Condizione: Brand New. 4th edition. 1051 pages. German language. 10.98x8.27x2.07 inches. In Stock.

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Taschenbuch. Condizione: 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. Condizione: 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.…

Gebunden. Condizione: 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.…

Condizione: 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. Condizione: 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 Print on Demand. …

Buch. Condizione: 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.…

Taschenbuch. Condizione: 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.…

Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Inhaltsangabe1. Wasser und Bioelemente.- 2. Kohlenhydrate.- 3. Lipide.- 4. Nucleotide und Polynucleotide (Nucleinsäuren).- 5. Aminosäuren und Polyaminosäuren (Proteine).- 6. Celluläre Organellen und Strukturen.- 7. Biokatalyse.- 8. Stoffwechsel und Funktion der Nucleinsäuren.- 9. Mechanismus und Regulation der Proteinbiosynthese.- 10. Viren.- 11. Genetisch bedingte Proteindefekte.- 12. Bioenergetik.- 13. Grundlagen des Intermediärstoffwechsels.- 14. Intermediärstoffwechsel I: Citratcyclus.- 15. Intermediärstoffwechsel II: Kohlenhydrate.- 16. Intermediärstoffwechsel III: Lipide.- 17. Intermediärstoffwechsel IV: Aminosäuren.- 18. Intermediärstoffwechsel V: Purine und Pyrimidine.- 19. Intermediärstoffwechsel VI: Häm und Gallenfarbstoffe.- 20. Wasser- und Elektrolythaushalt.- 21. Spurenelemente.- 22. Vitamine.- 23. Ernährung.- 24. Endokrine Gewebe I: Allgemeine Grundlagen.- 25. Endokrine Gewebe II: Die schnelle Stoffwechselregulation.- 26. Endokrine Gewebe III: Hypothalamisch-hypophysäres System und Zielgewebe.- 27. Endokrine Gewebe IV: Regulation des Wasser- und Elektrolythaushalts.- 28. Gastrointestinaltrakt.- 29. Leber.- 30. Blut.- 31. Muskelgewebe.- 32. Binde- und Stützgewebe.- 33. Nervengewebe.- 34. Immunsystem.- 35. Nieren und Urin.- 36. Tumorgewebe.- 1. Hinweisindex zum Gegenstandskatalog 'Chemie für Mediziner und Biochemie'.- 2. Hinweisindex zum Gegenstandskatalog 'Pathophysiologie/Pathobiochemie'. 1056 pp. Deutsch.…