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/vufind/Search/Results?lookfor=%22Haya%2C+Saturnino%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Haya%2C+Saturnino%22&type=Person&sort=year
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PubPharm (40)
1
Efficacy and safety evaluation of Fanhdi® , a plasma-derived factor VIII/ von Willebrand factor concentrate, in Von Willebrand's disease patients undergoing surgery or invasive procedures : A prospective clinical study
enthalten in:
Haemophilia : the official journal of the World Federation of Hemophilia
| 2022
von
Jimenez-Yuste, V.
|
Núñez, L.
|
Alvarez-Roman, M.
| +7
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2
Efficacy and safety evaluation of Fanhdi®, a plasma‐derived factor VIII/ von Willebrand factor concentrate, in Von Willebrand's disease patients undergoing surgery or invasive procedures : A prospective clinical study
enthalten in:
Haemophilia
| 2022
von
Jimenez‐Yuste, V.
|
Núñez, L.
|
Alvarez‐Roman, M.
| +7
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3
Management of acquired hemophilia A : results from the Spanish registry
enthalten in:
Blood advances
| 2021
von
Mingot-Castellano, M.
|
Pardos-Gea, J.
|
Haya, S.
| +35
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4
Clinical benefits of a Bayesian model for plasma-derived factor VIII/VWF after one year of pharmacokinetic-guided prophylaxis in severe/moderate hemophilia A patients
enthalten in:
Thrombosis research
| 2021
von
Megías-Vericat, J.
|
Bonanad, S.
|
Haya, S.
| +8
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5
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
enthalten in:
Journal of thrombosis and thrombolysis
| 2020
von
Moret, A.
|
Zúñiga, .
|
Ayala, J.
| +7
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6
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
enthalten in:
Journal of thrombosis and thrombolysis
| 2020
von
Moret, A.
|
Zúñiga, .
|
Ayala, J.
| +7
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7
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
enthalten in:
Journal of thrombosis and thrombolysis
| 2020
von
Moret, A.
|
Zúñiga, .
|
Ayala, J.
| +7
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8
Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
enthalten in:
Journal of thrombosis and thrombolysis
| 2020
von
Moret, A.
|
Zúñiga, .
|
Ayala, J.
| +7
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9
Prophylactic treatment in hemophilic patients with inhibitors
enthalten in:
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
| 2019
von
Haya, S.
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10
Clinical and molecular characterization by next generation sequencing of Spanish patients affected by congenital deficiencies of fibrinogen
enthalten in:
Thrombosis research
| 2019
von
Moret, A.
|
Zúñiga, .
|
Ibáñez, M.
| +6
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Medienart
40
Aufsätze
24
E-Artikel
24
E-Ressourcen
16
Gedruckte Aufsätze
Zeitschriftentitel
5
Haematologica
4
Annals of hematology
4
British journal of haematology
4
Haemophilia : the official journal of the World...
4
Journal of thrombosis and thrombolysis
3
Haemophilia
2
American journal of hematology
2
Blood
2
Haematologica, the hematology journal
2
The journal of laboratory and clinical medicine
2
Thrombosis research
1
Blood advances
1
Blood coagulation & fibrinolysis : an internati...
1
Clinical case reports
1
Thrombosis research / Supplement
1
Tijdschrift voor kindergeneeskunde
1
Translational research : the journal of laborat...
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Thema
10
9001-27-8
10
Factor VIII
9
Journal Article
7
Letter
7
Research Support, Non-U.S. Gov't
5
Genetics
4
Bleeding
4
FXIII deficiency
4
High-throughput sequencing
4
von Willebrand Factor
3
Factor VIII binding capacity
3
Low expression
3
Missense mutation
3
Type 2N
3
gene
3
von Willebrand disease
2
7NL2E3F6K3
2
839MOZ74GK
2
9001-28-9
2
Antibodies, Bispecific
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Erscheinungszeitraum
38
2000-
2
1900-1999
Erscheinungsjahr(e)
Von:
Bis:
Sprache
23
Englisch
1
Niederländisch
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