Haemophilia and rare bleeding disorders: molecular genetics, molecular pathology and clinical manifestation
Gespeichert in:
| Weitere Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | German English |
| Veröffentlicht: |
Lengerich ; Berlin ; Bremen ; Miami, Fla. ; Riga ; Viernheim ; Wien ; Zagreb
Pabst Science Publ.
2008
|
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | Beitr. teilw. dt., teilw. engl. - Literaturangaben |
| Beschreibung: | 234 S. graph. Darst. 21 cm, 323 gr. |
| ISBN: | 9783899674361 |
Internformat
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| 245 | 1 | 0 | |a Haemophilia and rare bleeding disorders |b molecular genetics, molecular pathology and clinical manifestation |c F. H. Herrmann (ed.) |
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Datensatz im Suchindex
| _version_ | 1804138502047137792 |
|---|---|
| adam_text | Contents
Contents
Hamophilie
Hemophilia in France: Epidemiology, Organisation of Cares, Registry
I.-F. Schved 13
Genetic Aspects on Inhibitor Development in Hemophilia
j. Astermark, E. Berntorp 16
Fa ktor-VII-M angel
Klinische Manifestation bei congenitalem Faktor VII Mangel
- Update des Creifswald-Registers Faktor-VII-Mangel -
F. H. Herrmann, K. Wulff, C. 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-Sanchez,
J. F. Schenk, C. Schubert, S. Schulman, ]. Wendisch und C. Vogel fiir die
Creifswald Faktor-FVII-Mangel-Studiengruppe 27
Bedeutung und Einfluss von Faktor-VII-Polymorphismen bei der
genomischen Diagnostik von erblich bedingtem FVII-Mangel
K. Wulff, C. Schuster, F. H. Herrmann und die
Internationale Studiengruppe des Creifswald Register Faktor VII 51
In-vitro-Charakterisierung von zwei neuen splice site Mutationen im
humanen FVII-Cen
W. Schroder, R. Tech, K. Wulff, U. Gobel, A. Ruiz-Saez, F. H. Herrmann 75
7
Contents
Charakterisierung einer donor splice site Mutation (g.64 G A) im
Exon 1 des FVII-Gens - Ein Fall von RNA-Editing?
W. Schroder, K. Wulff, R. Tech, C. Auerswald, S. Becker,
F. H. Herrmann 84
Der Einfluss von Faktor V HR2 auf die Thrombinbildung und die
klinische Auspragung seltener Blutungsdefekte
R. F. Strey, A. Siegemund, Th. Siegemund, C. Schubert, C. Schuster,
K. Wulff, F. H. Herrmann 91
Faktor-X-Mangel
Struktur und Funktion des Blutgerinnungsfaktors X und ihre Storung
durch Mutationen im Faktor-X-Gen
R. F. Strey, K. Wulff, W. Schroder, F. H. Herrmann 107
Klinische Manifestation bei congenitalem Faktor-X-Mangel
- Update des Greifswald-Registers Faktor-X-Mangel -
F. H. Herrmann, K. Wulff, C. Auerswald
M. Ark, 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, C. Marx, B. Mitulla,
B. Naumann, M. Navarrete, I. M. Carrillo, G. Pfanner, H. Pollmann,
A. Ruiz-Saez, L Salazar-Sanchez, I. Scharrer, E. Scharf, G. Syrbe,
M. v. Depka Prondzinsky, j. Wendisch, K. Wolf 138
Schwere intrakraniale Blutungen bei zwei Brudern mit FX-Mangel -
Charakterisierung einer homozygoten Acceptor splice site Mutation
im FX-Gen
W. Schroder, K. Wulff, B. Naumann, H. Pollmann, F. H. Herrmann 156
Fa ktor-X Ill-Mangel
Factor XIII Deficiency
V. Ivaskevicius, R. Seitz, E. Seifried, I. Oldenburg 165
8
Contents
Antithrombin-Mangel
Molecular Basis of Antithrombin Deficiency
A. Pavlova, B. Luxembourg, E. Lindhoff-Last, W. Kreuz, C. Heller,
H. Pollmann, U. Budde, R. Zimmermann, I. Scharrer, E. Seifried,
I. Oldenburg 177
Thrombophilie
The Thrombophilia Concept - What are the Developments until now?
C. Vogel 193
Analysis of Seven Recently Described Polymorphisms and their
Association with Deep Vein Thrombosis
R. Lauschus, C. Vogel, F. H. Herrmann, K. Wulff, W. Schroder,
E. Weber 201
Molecular Markers Associated with Thrombophilia in Costa Rican
Venous Thrombosis Patients
L. Salazar-Sanchez, M. P. Leon, M. Cartin, C. Schuster, K. Wulff,
W. Schroder, C. Jimenez-Arce, R. Chanon, F. H. Herrmann 209
List of Contributors (corresponding authors) 224
Farbabbildungen 226
9
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| dewey-search | 616.157 |
| dewey-sort | 3616.157 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| format | Book |
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| id | DE-604.BV035233354 |
| illustrated | Illustrated |
| indexdate | 2024-07-09T21:29:12Z |
| institution | BVB |
| isbn | 9783899674361 |
| language | German English |
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| spelling | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation F. H. Herrmann (ed.) Lengerich ; Berlin ; Bremen ; Miami, Fla. ; Riga ; Viernheim ; Wien ; Zagreb Pabst Science Publ. 2008 234 S. graph. Darst. 21 cm, 323 gr. txt rdacontent n rdamedia nc rdacarrier Beitr. teilw. dt., teilw. engl. - Literaturangaben Thrombophilie (DE-588)4059962-0 gnd rswk-swf Hämostasestörung (DE-588)4022824-1 gnd rswk-swf Hämophilie (DE-588)4072214-4 gnd rswk-swf (DE-588)1071861417 Konferenzschrift 2007 Greifswald gnd-content Hämophilie (DE-588)4072214-4 s DE-604 Hämostasestörung (DE-588)4022824-1 s Thrombophilie (DE-588)4059962-0 s Herrmann, Falko H. (DE-588)108735230 edt HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017039265&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation Thrombophilie (DE-588)4059962-0 gnd Hämostasestörung (DE-588)4022824-1 gnd Hämophilie (DE-588)4072214-4 gnd |
| subject_GND | (DE-588)4059962-0 (DE-588)4022824-1 (DE-588)4072214-4 (DE-588)1071861417 |
| title | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation |
| title_auth | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation |
| title_exact_search | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation |
| title_full | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation F. H. Herrmann (ed.) |
| title_fullStr | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation F. H. Herrmann (ed.) |
| title_full_unstemmed | Haemophilia and rare bleeding disorders molecular genetics, molecular pathology and clinical manifestation F. H. Herrmann (ed.) |
| title_short | Haemophilia and rare bleeding disorders |
| title_sort | haemophilia and rare bleeding disorders molecular genetics molecular pathology and clinical manifestation |
| title_sub | molecular genetics, molecular pathology and clinical manifestation |
| topic | Thrombophilie (DE-588)4059962-0 gnd Hämostasestörung (DE-588)4022824-1 gnd Hämophilie (DE-588)4072214-4 gnd |
| topic_facet | Thrombophilie Hämostasestörung Hämophilie Konferenzschrift 2007 Greifswald |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017039265&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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