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Haemophilia and Rare Bleeding Disorders – Molecular Genetics, Molecular Pathology and Clinical Manifestation | by Falko H. Herrmann (Ed.)

Category: Medicine/Medical books
Item number: ISBN 978-3-89967-436-1
Price: 25.00 EUR   (w/o VAT 23.36)
Info:
2008, 236 pages


Contents:

Hämophilie

J.-F. Schved:
Hemophilia in France: Epidemiology, Organisation of Cares, Registry

J. Astermark, E. Berntorp:
Genetic Aspects on Inhibitor Development in Hemophilia


Faktor-VII-Mangel

F. H. Herrmann, K. Wulff, G. Auerswald, J. Astermark, V. Aumann, A. Batorova, F. Bergmann, B. Eifrig, R. Eisert, D. Franke, U. Goebel, C. Heller, W. Kreuz, K. Kurnik, H. Lenk, R. M. Loreth, H. Pollmann, A. Ruiz-Saez, N. de Bosch, L. Salazar-Sánchez, J. F. Schenk, C. Schubert, S. Schulman, J. Wendisch und G. Vogel für die Greifswald Faktor-FVII-Mangel-Studiengruppe:
Klinische Manifestation bei congenitalem Faktor VII Mangel – Update des Greifswald-Registers Faktor-VII-Mangel –

K. Wulff, G. Schuster, F. H. Herrmann und die Internationale Studiengruppe des Greifswald Register Faktor VII:
Bedeutung und Einfluss von Faktor-VII-Polymorphismen bei der genomischen Diagnostik von erblich bedingtem FVII-Mangel

W. Schröder, R. Tech, K. Wulff, U. Göbel, A. Ruiz-Saez, F. H. Herrmann:
In-vitro-Charakterisierung von zwei neuen splice site Mutationen im humanen FVII-Gen

W. Schröder, K. Wulff, R. Tech, G. Auerswald, S. Becker, F. H. Herrmann:
Charakterisierung einer donor splice site Mutation (g.64 G>A) im Exon 1 des FVII-Gens – Ein Fall von RNA-Editing?

R. F. Strey, A. Siegemund, Th. Siegemund, C. Schubert, G. Schuster, K. Wulff, F. H. Herrmann:
Der Einfluss von Faktor V HR2 auf die Thrombinbildung und die klinische Ausprägung seltener Blutungsdefekte


Faktor-X-Mangel

R. F. Strey, K. Wulff, W. Schröder, F. H. Herrmann:
Struktur und Funktion des Blutgerinnungsfaktors X und ihre Störung durch Mutationen im Faktor-X-Gen

F. H. Herrmann, K. Wulff, G. Auerswald, M. Arlt, M. Barthels, A. Batorova, A. Boadas, N. de Bosch, F. Bergmann, U. Budde, R. Eisert, B. Eifrig, S. Halimeh, C. Hernandez, K. Kentouche, U. Kluba, K. Kurnik, S. Lopaciuk, B. Maak, G. Marx, B. Mitulla, B. Naumann, M. Navarrete, J. M. Carrillo, G. Pfanner, H. Pollmann, A. Ruiz-Saez, L. Salazar-Sánchez, I. Scharrer, E. Scharf, G. Syrbe, M. v. Depka Prondzinsky, J. Wendisch, K. Wolf:
Klinische Manifestation bei congenitalem Faktor-X-Mangel – Update des Greifswald-Registers Faktor-X-Mangel –

W. Schröder, K. Wulff, B. Naumann, H. Pollmann, F. H. Herrmann:
Schwere intrakraniale Blutungen bei zwei Brüdern mit FX-Mangel – Charakterisierung einer homozygoten Acceptor splice site Mutation im FX-Gen


Faktor-XIII-Mangel

V. Ivaskevicius, R. Seitz, E. Seifried, J. Oldenburg:
Factor XIII Deficiency


Antithrombin-Mangel

A. Pavlova, B. Luxembourg, E. Lindhoff-Last, W. Kreuz, C. Heller, H. Pollmann, U. Budde, R. Zimmermann, I. Scharrer, E. Seifried, J. Oldenburg:
Molecular Basis of Antithrombin Deficiency


Thrombophilie

G. Vogel:
The Thrombophilia Concept – What are the Developments until now?

R. Lauschus, G. Vogel, F. H. Herrmann, K. Wulff, W. Schröder, E. Weber:
Analysis of Seven Recently Described Polymorphisms and their Association with Deep Vein Thrombosis

L. Salazar-Sánchez, M. P. León, M. Cartín, G. Schuster, K. Wulff, W. Schröder, G. Jiménez-Arce, R. Chanon, F. H. Herrmann:
Molecular Markers Associated with Thrombophilia in Costa Rican Venous Thrombosis Patients

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