Abstract Index

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F
Factor V Inhibitor Acquired after Exposure to High-Purity Topical Bovine Thrombin during Orthopedic Surgery
Harris SB, Benson E, Duncan A
 
Factor V Kuwait: a New Point Mutation in the Coagulation Factor V Gene
Jadaon MM, Dashti AA
 
Factor V Leiden and Aprotinin in Cardiopulmonary Bypass
Linden MD, Schneider M, Erber WN
 
Factor V Leiden and Prothrombin G20210A Mutations in Children with Cerebral Palsy
Ulutin T, Tezol A, Yüksel A, Buyearu N
 
Factor V Leiden and R2 Mutations, Prothrombin G20210A Mutation and Osteonecrosis
Zalavras C, Malizos K, Dova L, Zibis A, Dokou E, Dailiana Z, Kolaitis N, Vartholomatos G
 
Factor V Leiden as a Modifier of the Severe Hemophilia Phenotype in Murine Models
Schlachterman A, Liu J, Liu Y-L, Camire RM, Arruda VR
 
Factor V Leiden Mutation and Pregnancy Associated Venous Thromboembolism: A Meta-Analysis
Biron-Andreani C, Schved JF, Daures JP
 
Factor V Leiden: An Important Risk Factor for Venous and Arterial Thrombosis in Brazilian Patients
Sabino AP, Ribeiro DD, Guimarães DAM, Soares AL, Carvalho MG, Fernandes AP, Dusse LMS, Vieira LM, Cardoso JE
 
Factor V Mutations, Arg2174Leu, a 5-bp Deletion and Val1813Met, Are Associated with Factor V Deficiency and A Bleeding Tendency
Shinozawa K, Inaba H, Amano K, Suzuki T, Takahashi H, Iijima K, Tanaka A, Arai M, Fukutake K
 
Factor Va Membrane Binding Affinity and Prothrombinase Activity are Enhanced by Incorporation of Phosphatidylethanolamine into Phosphatidylserine Containing Membranes
Liang X, Quinn-Allen MA, Kane WH
 
Factor VII Activating Protease (FSAP) Inhibits Angiogenesis in vivo
Kanse SM, Linn T, Sürücü O, Matz R, Henning S, Dietz C, Weimer T, Preissner KT, Celik I
 
Factor VII Arg277His Mutation Induced Discrepancy of Factor VII Activity Levels Using Tissue Factor from Different Sources
Tarumi T, Kanazawa K, Ieko M, Mizukami M, Yoshida M, Naito S, Nakabayashi T, Notoya A, Koike T
 
Factor VIIa Binding and Internalization in Hepatocytes
Hjortoe GM, Sorensen BB, Petersen LC, Rao LVM
 
Factor VIII / LRP Interactions
 
Factor VIII Activity and Antigen, VWF and ABO-Genotype Are Not Associated with Coronary Heart Disease
Bach J, Preiss A, Haubelt H, Winkelmann BW, Maerz W, Boehm B, Hellstern P
 
Factor VIII and von Willebrand Factor Changes after Desmopressin and During Pregnancy in Type 2M von Willebrand Disease Vicenza: A Prospective Study Comparing Patients with Single (R1205H) and Double (R1205H-M740I) Defect
Castaman G, Federici AB, Bernardi M, Moroni B, Bertoncello K, Rodeghiero F
 
Factor VIII Coagulant Activity and Antigen Levels Increase the Risk of Venous Thrombosis; Results of the MEGA Study
Doggen CJM, Bertina RM, Rosendaal FR
 
Factor VIII Expression Induces ER Stress Apoptosis In Cultured Cells and in Mice
Malhotra J, Maio H, Pipe SW, Kaufman RJ
 
Factor VIII Inhibitor in a Patient with Mild Haemophilia A
Santoro R, Iannaccaro P, Muleo G
 
Factor VIII Inhibitors in Hemophilia A during Immune Tolerance Induction
van Helden PMW, Gouw SC, Mauser-Bunschoten EP, van den Berg HM, Voorberg J
 
Factor VIII Inhibitors in Mild Haemophilia A. Incidence in Patients with Arg2150His Mutation in South of Spain
Perez R, Nuñez R
 
Factor VIII Levels and Blood Coagulation in Patients on Long-Term Oral Anticoagulation (OA)
Brzezinska-Kolarz B, Undas A, Padjas A, Iwaniec T, Musial J
 
Factor VIII Mimetic Antibody: (1) Establishment and Characterization of Anti-factor IX/Anti-factor X Bispecific Antibodies
Saito H, Kojima T, Miyazaki T, Soeda T, Kitazawa T, Suzuki T, Yoshihashi K, Adachi H, Nezu J, Shima M, Yoshioka A, Hattori K
 
Factor VIII Mimetic Antibody: (2) In Vitro Assessment of Cofactor Activity in Hemophilia A
Shima M, Matsumoto T, Sakurai Y, Takeyama M, Tanaka I, Saito H, Hattori K, Yoshioka A
 
Factor VIII Mutation Type in Severe and Moderate Haemophilia A, and Inhibitor Development in a Congenital Coagulopathies Unit
Haya S, Casaña P, Cabrera N, Cid AR, Cortina V, Querol F, Aznar JA
 
Factor VIII Residues 97–105 and 1954–1961 of the A1 and A3 Domains Represent an Inter-Subunit Interface
Ansong CA, Miles SM, Fay PJ
 
Factor VIII:c Levels in Subjects with the Factor V R2Ppolymorphism
Martinelli N, Girelli D, Lunghi B, Olivieri O, Scanavini D, Manzato F, Lotto V, Tenuti I, Bozzini C, Friso S, Pizzolo F, Corrocher R, Bernardi F
 
Factor VIIIa Regulates Substrate Delivery to the Intrinsic Factor X-Activating Complex
Panteleev MA, Ananyeva NM, Greco NJ, Ataullakhanov FI, Saenko EL
 
Factor X Deficiency: Clinical Manifestation of 102 Subjects with Mutations in Factor 10 Gene
Herrmann FH, Auerswald G, Ruiz-Saez A, Navarette M, Pollmann H, Lopaciuk S, Batorova A, Wulff K
 
Factor X Gene Mutations Affecting the Gla Domain of the Protein
Akhavan S, Chafa O, Nsoure Obame F, Serve E, Torchet M-F, Reghis A, Fischer A-M, Tapon-Bretaudière J
 
Factor Xa-Directed Inhibition in Plasma from Patients Undergoing Coumadin Treatment: Observations Relevant to Bridging Therapy
Gould WR, Shafer SS, Leadley Jr RJ
 
Factor XI Deficient Mice Have Reduced Platelet Accumulation and Fibrin Deposition after Laser Injury
Baird TR, Gailani D, Furie, Br1,2 , Furie Ba
 
Factor XII (fXII) Is Activated by Unfolded Proteins on the Surface of Negatively Charged Substances, Rather than by These Surfaces Themselves
Bouma B, Maas C, Schiks B, de Groot PhG, Gebbink MFBG
 
Factor XIII Levels and Factor XIII a Subunit Val34Leu Polymorphism in Patients with Coronary Sclerosis and Myocardial Infarction
Katona É, Bereczky Z, Balogh E, Czuriga I, Kárpáti L, Édes I, Muszbek L
 
Factor XIII Val34Leu Polymorphism in Croatian Population
Broni[cacute] A, Feren[ccaron]ak G, Zadro R, Stavljeni[cacute] Rukavina A
 
Factor XIII Val34Leu Polymorphism Showed an Adverse Pharmacogenetic Effect on the Thrombolytic Therapy for Acute Myocardial Infarction
Marín F, González-Conejero R, Lee KW, Corral J, Roldán V, López F, Sogorb F, Caturla J, Lip GYH, Vicente V
 
Factors Therapy in Surgical Patients without Hemophilia
Roitman E
 
Failure of Anticoagulation in Kawasaki Disease
Girisch M, Wiegand G, Rauch R
 
Failure of the Outpatient Bleeding Risk Index to Predict Major Bleeding in Older Patients Receiving Coumarin for Atrial Fibrillation
Ceresetto JM, Duboscq C, Rabinovich O, Stemmelin G, Shanley C, Doti C, Vicente MA, Gonzalez Vucovik M, Bullorsky E
 
False Positives Account For Low Conversion Frequency In Chimeraplasty For Von Willebrand Disease
De Meyer SF, Pareyn I, Baert J, Deckmyn H, Vanhoorelbeke K
 
Family with Inherited f.X Deficiency. Case Report
Plahuta TG, Larina LE, Svirin PV, Shiller EE, Soskov GI
 
Fatal Hemorrhagic Disorder and Vascular Intimal Carcinomatosis in Annexin II Expressing Transitional Cell Carcinoma
Seiji M, Mitsugu H, Hiroshi K, Tsukasa O, Teruko S, Jun M, Keiya O, Ken S, Yoichi S
 
Fatal Pulmonary Embolism and Cancer. A Study of 21 500 Post-Mortems over 35 years
Cohen AT, Weston GJ, Tasker AJ, Fellows GA, Wilmott R
 
Fatal Vascular Outcomes Following Major Orthopedic Surgery
Dahl OE, Caprini JA, Colwell Jr. CW, Frostick SP, Haas S, Hull RD, Laporte S, Stein PD
 
Favorable Outcome in the Pregnancy behind Treatment with Heparin in Women with Mutation of Methylenetetrahydrofolate Reductase (MTHFR) Gene and Fetal Loss Previous
Fisac Herrero R, Santamaria R, Olivier C, Hernandez J, Queizan J, Fisac Martin M, Martinez M, Calmuntia M
 
Favourable Pregnancy Outcome in Women with a History of Venous Thromboembolism and Prophylactic Low Molecular Weight Heparin (LMWH)
Alguel G, Vormittag R, Kyrle PA, Quehenberger P, Mannhalter C, Pabinger I
 
FcgRIIa Platelet Polymorphism in Asian Indians: Its Association with Development of Heparin Induced Thrombocytopenia
Kannan M, Ahmad F, Ahmad S, Kale S, Fareed J, Saxena R
 
FEIBA – Mode of Action
TurecekVáradi PLK, Gritsch H
 
FEIBA Use for Acquired Hemophilia
Boggio L
 
Fetal Loss in Hereditary Antithrombin, Protein C and Protein S Deficiencies
Korteweg FJ, Brouwer JLP, Folkeringa N, Veeger NJGM, Erwich JJHM, Holm JP, van der Meer J
 
Fgf-Receptor Signalling is Involved in Differentiation and Recruitment of Bone Marrow Progenitor Cells into Endothelial Progenitor Cells
Fons P, Hérault J-P, Géronimi F, Guéguen G, Delesque N, Challier C, Laplace M-C, Tuyaret J, Schaeffer P, Savi P, Bono F, Herbert J-M
 
Fibrin and b-chain Peptide (441–461) for Tissue Engineering Improves Tolerability and Efficiency of Non-viral Gene Vector Formulations
Stemberger A, Kullmer M, Koch C, Schillinger U, Plank C
 
Fibrin and Other Ligands Regulate the Kinetics of Non-proteolytic Active Site Formation in Plasminogen
 
Fibrin Clot Deformability: Influence of Fibrinogen Concentration
Savushkin AV
 
Fibrin D-Dimer, by Three Different Assays, is an Independent Predictor of Future Stroke in Patients With Atrial Fibrillation
Tait RC, Rumley A, McMahon AD, Murdoch DL, O’Neill KF, Wallace IW, Lowe GDO
 
Fibrin Monomers in the Diagnosis of Deep Vein Thrombosis
Schutgens REG, Haas FJLM, Biesma DH
 
Fibrin-Monomer Prepared Using Thrombin-Like Enzyme from Snake Venom Agkistrodon Halys as Stimulator of Plasminogen Activation By t-PA
Moukhametova LI, Aisina RB, Boulyguine OY, Varfolomeyev SD
 
Fibrinogen and Fibrin Structure and Functions
Mosesson MW
 
Fibrinogen May Predict Death from Cancer in Men with Lower Extremity Arterial Disease
MacCallum PK, Cooper JA, Meade TW
 
Fibrinogen Paris IX: A Case of Symptomatic Hypofibrinogenaemia Associated With Bbeta Y236C and Bbeta IVS7 -1G > C Mutations
Horellou MH, Chevreaud C, Mathieux V, Conard J, de Mazancourt P
 
Fibrinogen Storage Disease with Hypofibrinogenaemia
Santoro R, Iannaccaro P, Muleo G
 
Fibrinogen Variants of the Gamma Chain Coiled-Coil Portion Detected by Reverse Phase HPLC in Patients with Venous Thrombosis
Hanss MML, Vergnes C, Berruyer M, Ffrench PO, Dargaud Y, Rousson R, De Mazancourt P
 
Fibrinogen, Plasminogen Activator Inhibitor-1, and Interleukin-6 in Peripheral Arterial Disease of Type 2 Diabetes Patients
Hutajulu SH, Kurnianda J, Asdie RH, Wiyono P, Asdie AH
 
Fibrinogen-Aa Thr 312 Ala and Factor XIII Val 34 Leu Polymorphisms in Idiopathic Venous Thromboembolism
Le Gal G, Delahousse B, Regina S, Malaviolle V, Lacut K, Oger E, Mottier D, Gruel Y
 
Fibrinolytic Activity in the Patients with Buerger's Disease and PAOD
Terlecki P, Przywara S, Zubilewicz T, Feldo M, Ilzecki M, Kesik J, Wronski J
 
Fibrinolytic Activity Is Enhanced after Major Orthopedic Surgery
O'Donnell M, Stafford A, Johnston M, Fredenburgh JC, Weitz JI
 
Fibrinolytic Gene Polymorphism and Ischemic Stroke
Jood K, Ladenvall P, Tjärnlund Wolf A, Ladenvall C, Andersson M, Nilsson S, Blomstrand C, Jern C
 
Fibrinolytic Peritoneal Response to Laparoscopic Surgery
Duboscq C, Amarillo H, Roca J, Ceresetto JM, Shanley C, Stemmelin G, Rabinovich O, Doti C, Porto E, Bullorsy EO
 
Fibronectin-Binding Protein (FnBP) Mediates Staphylococcus Aureus-Induced Platelet Aggregation
Fitzgerald JR, Loughman A, Brennan M, Knobel M, Higgins J, Speziale P, Cox D, Foster TJ
 
Fine Epitope Mapping of Human Monoclonal Antibodies Directed Against the B Domain of Factor VIII
Lavigne-Lissalde G, Lacroix-Desmazes S, Schved JF, Granier C, Kaveri SV, Villard S
 
Fine Mapping of the Prothrombin Binding Site in the Apple 1 Domain of Factor XI
Baglia FA, Gailani D, Papagrigoriou V, Emsley J, Walsh pN
 
First Case of Compound Heterozygous Mutations in the Kininogen Gene Causing Severe High-Molecular-Weight Kininogen Deficiency
Geisen C, Grünewald M, Renne T, Watzka M, Muller-Esterl W, Seifried E, Oldenburg J
 
First Line Therapy with FEIBA® for the Intracranial Hemorrhages in Haemophilia Patients with Inhibitors
Musso R, Cultrera D, Musso M, Cipolla A, Giustolisi R
 
Fish Skins as a Source of Heparin-Like GAGs
Coyne E, Jeske WP, McDonald MK, Maddineni J, Mendes A, Dietrich CP, Walenga JM
 
FIX Activation on the Surface of Activate Platelets by rFVIIa in the Absence of Tissue Factor
Gabriel DA, Monroe DM, Roberts HR
 
FLEXTRA: Early vs Delayed Initiation of Postoperative Fondaparinux Prophylaxis after Joint Replacement: A Clinical Outcome Study
Davidson BL, Turpie AGG, Kwong LM, Colwell CW,  Jr 
 
Flow Cytometric Analysis of Platelet Activation Via Recombinant Factor VIIa
Nolen JDL, Webber B, Duncan A
 
Fluorescence-Based Study of Nonsense Mutation Suppression in Coagulation Factor VII Deficiency
Pinotti M, Rizzotto L, Pinton P, Ferraresi P, Chuansumrit A, Charoenkwan P, Canella A, Marchetti G, Rizzuto R, Mariani G, Bernardi F
 
Following Cardiac Surgery Patients Who Develop Biphasic Waveforms as Seen on the MDA-180 Automated Coagulation Analyser Have Increased Thrombin Potential in-vitro. This Is Partly due to Tissue Factor Present in the CRP-VLDL Complex
Davidson SJ, Al-Mazedi M, Burman JF
 
Follow-Up of Patients with Acute Venous Thromboembolism Treated with Ximelagatran for Prophylaxis of Recurrent Events
Harenberg J, Jörg I, Müller G, Öttler W, Diehm C, Stein U, Schellong S
 
Fondaparinux Combined with Intermittent Pneumatic Compression (IPC) Versus IPC Alone in the Prevention of VTE after Major Abdominal Surgery: Results of the APOLLO Study
Turpie AG, Bauer K, Caprini J, Comp P, Gent M, Muntz J
 
Fondaparinux Use in Heparin-Induced Thrombocytopenia
Boggio L, Soff G, Zakarija A, Green D
 
Food Intake Enhances Platelet Reactivity to Thromboxane in Type 2 Diabetic Patients
Li N, Yngen M, Daleskog M, Johansson M-C, Wallén NH, Östenson C-G, Hjemdahl P
 
Four Direct Thrombin Inhibitors (DTIs) Variably Increase the Prothrombin Time: A Consequence of Differing Therapeutic Molar Concentrations?
Warkentin TE, Greinacher A, Craven S, Dewar L, Sheppard JI, Ofosu FA
 
Four Novel Missense Mutations in Factor IX Gene Were Identified as Causes of Hemophilia B
Shu A, Suzuki T, Shinozawa K, Inaba H, Tsujikawa A, Kokaji T, Arai M, Fukutake K
 
Fractalkine Mediates Leukocyte Recruitment to Inflammatory Endothelial Cells in Flowing Whole Blood
Schulz C, Schafer A, Stolla M, Lorenz M, Bauersachs J, Gawaz M, Massberg S
 
Frequency of Anticardiolipin (aCL) Antibodies in Patients with Lupus Anticoagulant (LA) Detected by Different Methods: An Analysis of 4265 Cases
Franco RF, Matos MF, Leser PG, Villela MSH, Figueiredo MS
 
Functional Analyses of the Reconstituted AlphaIIbbeta3 and AlphaVbeta3 Minireceptors
Bledzka-Krupska K, Michalec L, Szymanski J, Kish M, Plow EF, Cierniewski CS
 
Functional Analysis o Two Recombinant Missense Mutant Factor XI, F221S ad C212R
Kuroda K, Morishita E, Hirano K, Yamazaki K, Sekino T, Yamazaki M, Asakura H, Nakao S, Ohtake S
 
Functional Analysis of A -13 G/A Dimorphism at the Major Transcription Initiation Site of the Protein Z Gene
Winship PR, Haridas S, Wragg MM, Prasad S, Hall AJ
 
Functional Analysis of Obligate Heterozygous Defects in Platelet Glycoprotein (GP) Ib-V-IX in Velo-Cardio-Facial Syndrome (VCFS) Patients
Liang HPH, Morel-Kopp MC, Curtin J, Wilson M, Hewson J, Ward CM
 
Functional Analysis of the Factor Ix Egf-Like Domain Mutation Ile66thr Associated with Mild Hemophilia B
Knobe KE, Persson KEM, Sjörin E, Villoutreix BO, Ljung RCR
 
Functional Characterization of the FXIII Cross Linking Sites in the Fibrinogen g-Chain
Standeven KF, Carter AM, Masova L, Lord ST, Weisel JW, Grant PJ, Ariëns RAS
 
Functional Decrease in Thrombin Activatable fibrinolytic Inhibitor by Anticoagulant Drugs: A Possible Explanation for the Observed Profibrinolytic Actions
Florian-Kujawski M, Hoppensteadt D, Maddineni J, Wilmer M, Ziegler H, Fareed J
 
Functional Differences in the Response of Platelets to Collagen That Are Linked to Glycoprotein VI Genotype Are Also Associated with Differences in Platelet Gene Expression Profiles
Carr P, Macaulay IC, Dudbridge F, Tom B, Langford CF, Smethurst PA, Watkins NA, Ouwehand WH
 
Functional Duplication of Ligand-Binding Domains within Low-Density Lipoprotein Receptor-Related Protein for Interaction with Alpha2-Macroglobulin, Factor IXa and Factor VIII
Meijer AB, Rohlena J, van der Zwaan C, Boertjes RC, Lenting PJ, Mertens K
 
Functional Evidence for Three I-domain Activation States for Platelet a2b1 Integrin
Siljander P, Schoolmeester A, Smerling C, Van de Walle G, Hamaia S, Deckmyn H, Farndale RW
 
Functional Role of Human P-Selectin (CD62P) Polymorphisms in Mediating Cell-Cell Interactions
Barek L, Touka MA, Cerutti C, Barbaux S, Cambien F, McGregor JL
 
Further Characterization of the Mutation in Blade 2 of the aIIb b-Propeller That Causes Glanzmann Thrombasthenia in Palestinian Arabs
Rosenberg N, Hauschner H, Landau M, Seligsohn U
 
Further Evidence for Ping-Pong-Like Mechanism for Prothrombinase from Analysis of the Time Courses of Prothrombin, Meizothrombin, Prethrombin-2, and Thrombin During Prothrombin Activation
Kim PY, Nesheim ME
 
Fusion of the N-terminal Acidic Domain of Heparin Cofactor II to a1-PI M358R Increases the Rate of Thrombin Inhibition
Sutherland JS, Bhakta V, Filion ML, Sheffield WP
 
FV Leiden Mitigates Bleeding Tendency in Recessive Type 1 von Willebrand Disease
Casonato A, Sartorello F, Pontara E, Marcato S, Cattini MG, Simioni P, Gallinaro L, Bertomoro A, Pagnan A
 
FVII Deficiency due to Homozygous FVII T324M Mutation
Kemball-Cook G, Gomez K, Roscioli T, McVey JH
 
FVIIa Decreases Surgery-Induced IL-6 Response in Burn Patients Undergoing Excision and Skin Grafting
Olsen EHN, Johansson PI, Eriksen K, Nielsen SL, Alsbjørn B, Rojkjaer R
 
FVIII-Dependent Propagation Phase Is of Minor Importance During Septic Peritonitis
Brüggemann LW, Schoenmakers SHHF, Reitsma PH, Spek CA
 
FXI Deficiency in South Australia: Diversity of Causative Mutations within a Small Group of Affected Individuals
Duncan EM, Fenech M, Casey G, Casey CR, Rodgers SE, Lee SH, Chunilal S, Lloyd JV