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La ricerca find articoli where soggetti phrase all words 'prothrombin gene' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 177 riferimenti
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    1. Turri, D; Rosselli, M; Simioni, P; Tormene, D; Grimaudo, S; Martorana, G; Siracusa, S; Mariani, G; Cottone, M
      Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area

      DIGESTIVE AND LIVER DISEASE
    2. Haslam, N; Standen, GR; Probert, CS
      An investigation of the association of the prothrombin G20210A gene mutation and inflammatory bowel disease: Factor II and IBD

      INFLAMMATORY BOWEL DISEASES
    3. Ghosh, K; Shetty, S; Madkaikar, M; Pawar, A; Nair, S; Khare, A; Pathare, A; Jijina, F; Mohanty, D
      Venous thromboembolism in young patients from Western India: A study

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    4. Pickering, W; Marriott, K; Regan, L
      G20210A prothrombin gene mutation: Prevalence in a recurrent miscarriage population

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    5. Olah, L; Misz, M; Kappelmayer, J; Ajzner, E; Csepany, T; Fekete, I; Bereczki, D; Blasko, G; Csiba, L
      Natural coagulation inhibitor proteins in young patients with cerebral ischemia

      CEREBROVASCULAR DISEASES
    6. Kuker, W; Schmidt, F; Friese, S; Block, F; Weller, M
      Unilateral thalamic edema in internal cerebral venous thrombosis: Is it mostly left?

      CEREBROVASCULAR DISEASES
    7. Ferro, JM; Correia, M; Pontes, C; Baptista, MV; Pita, F
      Cerebral vein and dural sinus thrombosis in Portugal: 1980-1998

      CEREBROVASCULAR DISEASES
    8. Cosmi, B; Legnani, C; Bernardi, F; Coccheri, S; Palareti, G
      Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study

      BRITISH MEDICAL JOURNAL
    9. Sprouse, JT; Wong, CS; Chandler, WL; Williams, GD; Watkins, SL; Tarr, PI
      Thrombogenic alleles, Escherichia coli O157 : H7 infections, and hemolyticuremic syndrome

      BLOOD COAGULATION & FIBRINOLYSIS
    10. Cutler, JA; Mitchell, MJ; Greenslade, K; Smith, MP; Savidge, GF
      A rapid and cost-effective method for analysis of three common genetic risk factors for thrombosis

      BLOOD COAGULATION & FIBRINOLYSIS
    11. Kearon, C
      Duration of anticoagulation for venous thromboembolism

      JOURNAL OF THROMBOSIS AND THROMBOLYSIS
    12. Nowak-Gottl, U; Strater, R; Kosch, A; von Eckardstein, A; Schobess, R; Luigs, P; Nabel, P; Vielhaber, H; Kurnik, K; Junker, R
      The plasminogen activator inhibitor (PAI)-1 promoter 4G/4G genotype is notassociated with ischemic stroke in a population of German children

      EUROPEAN JOURNAL OF HAEMATOLOGY
    13. Verdu, A; Cazorla, MR; Granados, MA; Alonso, JA; Casado, LF
      Basilar artery thrombosis in a child heterozygous for factor V Leiden mutation

      PEDIATRIC NEUROLOGY
    14. Incorvaia, C; Parmeggiani, F; Costagliola, C; Lamberti, G; Ferraresi, P; Bernardi, F; Sebastiani, A
      The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    15. Soria, JM; Baiget, M; Castano, L; Tejada, MI; Perez-Nanclares, G; Fontcuberta, J
      Genetic risk factors for thrombosis in a Basque population and their possible contribution to the analysis of a complex disease such as thrombophilia

      HAEMATOLOGICA
    16. Margaglione, M; Brancaccio, V; Ciampa, A; Papa, ML; Grandone, E; Di Minno, G
      Inherited thrombophilic risk factors in a large cohort of individuals referred to Italian thrombophilla centers: distinct roles in different clinicalsettings

      HAEMATOLOGICA
    17. Tormene, D; Simioni, P; Prandoni, P; Luni, S; Zerbinati, P; Sartor, D; Franz, F; Girolami, A
      Factor V Leiden mutation and the risk of venous thromboembolism in pregnant women

      HAEMATOLOGICA
    18. Leebeek, FWG; Stadhouders, NAM; van Stein, D; Gomez-Garcia, EB; Kappers-Klunne, MC
      Hypercoagulability states in upper-extremity deep venous thrombosis

      AMERICAN JOURNAL OF HEMATOLOGY
    19. Marcucci, R; Bertini, L; Giusti, B; Brunelli, T; Fedi, S; Cellai, AP; Poli, D; Pepe, G; Abbate, R; Prisco, D
      Thrombophilic risk factors in patients with central retinal vein occlusion

      THROMBOSIS AND HAEMOSTASIS
    20. Glueck, CJ; Fontaine, RN; Wang, P
      Interaction of heritable and estrogen-induced thrombophilia: Possible etiologies for ischemic optic neuropathy and ischemic stroke

      THROMBOSIS AND HAEMOSTASIS
    21. Heckmann, JG; Tomandl, B; Erbguth, F; Neidhardt, B; Zingsem, H; Neundorfer, B
      Cerebral vein thrombosis and prothrombin gene (G20210A) mutation

      CLINICAL NEUROLOGY AND NEUROSURGERY
    22. Bertina, RM
      Genetic aspects of venous thrombosis

      EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
    23. Fischereder, M; Schneeberger, H; Lohse, P; Kramer, BK; Schlondorff, D; Land, W
      Increased rate of renal transplant failure in patients with the G20210A mutation of the prothrombin gene

      AMERICAN JOURNAL OF KIDNEY DISEASES
    24. Mohanty, D; Shetty, S; Ghosh, K; Pawar, A; Abraham, P
      Hereditary thrombophilia as a cause of Budd-Chiari syndrome: A study from western India

      HEPATOLOGY
    25. Akar, N; Akar, E; Ozel, D; Deda, G; Sipahi, T
      Common mutations at the homocysteine metabolism pathway and pediatric stroke

      THROMBOSIS RESEARCH
    26. Hankey, GJ; Eikelboom, JW; van Bockxmeer, FM; Lofthouse, E; Staples, N; Baker, RI
      Inherited thrombophilia in ischemic stroke and its pathogenic subtypes

      STROKE
    27. Strater, R; Kurnik, K; Heller, C; Schobess, R; Luigs, P; Nowak-Gottl, U
      Aspirin versus low-dose low-molecular-weight heparin: Antithrombotic therapy in pediatric ischemic stroke patients - A prospective follow-up study

      STROKE
    28. Abramson, N; Abramson, S
      Hypercoagulability: Clinical assessment and treatment

      SOUTHERN MEDICAL JOURNAL
    29. Petaja, J; Hiltunen, L; Fellman, V
      Increased risk of intraventricular hemorrhage in preterm infants with thrombophilia

      PEDIATRIC RESEARCH
    30. Seligsohn, U; Lubetsky, A
      Medical progress: Genetic susceptibility to venous thrombosis.

      NEW ENGLAND JOURNAL OF MEDICINE
    31. O'Shaughnessy, KM; Fu, BY; Downing, S; Morris, NH
      Thrombophilic polymorphisms in pre-eclampsia: altered frequency of the functional 98C > T polymorphism of glycoprotein IIIa

      JOURNAL OF MEDICAL GENETICS
    32. Hessner, MJ; Dinauer, DM; Kwiatkowski, R; Neri, B; Raife, TJ
      Age-dependent prevalence of vascular disease-associated polymorphisms among 2689 volunteer blood donors

      CLINICAL CHEMISTRY
    33. Chak, M; Wallace, GR; Graham, EM; Stanford, MR
      Thrombophilia: genetic polymorphisms and their association with retinal vascular occlusive disease

      BRITISH JOURNAL OF OPHTHALMOLOGY
    34. De Stefano, V; Martinelli, I; Mannucci, PM; Paciaroni, K; Rossi, E; Chiusolo, P; Casorelli, I; Leone, G
      The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation

      BRITISH JOURNAL OF HAEMATOLOGY
    35. Lind, B; Koefoed, P; Thorsen, S
      Symptomatic type 1 protein C deficiency caused by a de novo Ser270Leu mutation in the catalytic domain

      BRITISH JOURNAL OF HAEMATOLOGY
    36. Federman, DG; Kirsner, RS
      An update on hypercoagulable disorders

      ARCHIVES OF INTERNAL MEDICINE
    37. Thomas, RH
      Hypercoagulability syndromes

      ARCHIVES OF INTERNAL MEDICINE
    38. Leiba, M; Sidi, Y; Gur, H; Leiba, A; Ehrenfeld, M
      Behcet's disease and thrombophilia

      ANNALS OF THE RHEUMATIC DISEASES
    39. Bauer, KA
      The thrombophilias: Well-defined risk factors with uncertain therapeutic implications

      ANNALS OF INTERNAL MEDICINE
    40. Amitrano, L; Brancaccio, V; Guardascione, MA; Margaglione, M; Iannaccone, L; D'Andrea, G; Ames, PRJ; Marmo, R; Mosca, S; Balzano, A
      High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    41. Botto, LD; Khoury, MJ
      Commentary: Facing the challenge of gene-environment interaction: The two-by-four table and beyond

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    42. Miao, CH; Ohashi, K; Patijn, GA; Meuse, L; Ye, X; Thompson, AR; Kay, MA
      Inclusion of the hepatic locus control region, an intron, and untranslatedregion increases and stabilizes hepatic factor IX gene expression in vivo but not in vitro

      MOLECULAR THERAPY
    43. Spek, CA; Reitsma, PH
      Genetic risk factors for venous thrombosis

      MOLECULAR GENETICS AND METABOLISM
    44. Kukuczka, SM; Grosso, LE
      Efficient recovery of DNA from peripheral blood for diagnostic analysis with a vacuum manifold

      MOLECULAR DIAGNOSIS
    45. Arnaud, E; Nicaud, V; Poirier, O; Rendu, F; Alhenc-Gelas, M; Fiessinger, JN; Emmerich, J; Aiach, M
      Protective effect of a thrombin receptor (protease-activated receptor 1) gene polymorphism toward venous thromboembolism

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    46. Mira, Y; Aznar, J; Estelles, A
      Congenital and acquired thrombotic risk factors in women using oral contraceptives: Clinical aspects

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    47. Angelopoulou, K; Nicolaides, A; Deltas, CC
      Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    48. Couturaud, F; Kearon, C
      Long-term treatment for venous thromboembolism

      CURRENT OPINION IN HEMATOLOGY
    49. Weih, M; Vetter, B; Castell, S; Ziemer, S; Kulozik, AE; Einhaupl, KM
      Hereditary thrombophilia in cerebral venous thrombosis

      CEREBROVASCULAR DISEASES
    50. Ruggeri, M; Castaman, G; Tosetto, A; Rodeghiero, F
      Two families with combined homozygous/heterozygous factor V Leiden mutation and heterozygous G20210A factor II variant

      BLOOD COAGULATION & FIBRINOLYSIS
    51. Bauduer, F; Claracq, M; Orgogozo, F; Mariescu, M; Ducout, L; Freyburger, G
      Mesenteric venous thrombosis in a 40-year-old man with homozygous factor II G20210A mutation

      BLOOD COAGULATION & FIBRINOLYSIS
    52. Torresan, M; Machado, TFGS; Siqueira, LH; Ozelo, MC; Arruda, VR; Annichino-Bizzacchi, JM
      The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis

      BLOOD COAGULATION & FIBRINOLYSIS
    53. Papa, A; De Stefano, V; Gasbarrini, A; Chiusolo, P; Cianci, R; Casorelli, I; Paciaroni, K; Cammarota, G; Leone, G; Gasbarrini, G
      Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation ininflammatory bowel disease

      BLOOD COAGULATION & FIBRINOLYSIS
    54. Backhouse, O; Parapia, L; Mahomed, I; Lee, D
      Familial thrombophilia and retinal vein occlusion

      EYE
    55. Couturaud, F; Grand'Maison, A; Kearon, C
      Optimal duration of anticoagulation for venous thromboembolism

      PRESSE MEDICALE
    56. Sivera, P; Bosio, S; Bertero, MT; Demaestri, M; Mazza, U; Camaschella, C
      G20210A homozygosity in antiphospholipid syndrome secondary to systemic lupus erythematosus

      HAEMATOLOGICA
    57. Angchaisuksiri, P; Pingsuthiwong, S; Aryuchai, K; Busabaratana, M; Sura, T; Atichartakarn, V; Sritara, P
      Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population

      AMERICAN JOURNAL OF HEMATOLOGY
    58. Liu, XY; Gabig, TG; Bang, NU
      Combined heterozygosity of factor V Leiden and the G20210A prothrombin gene mutation in a patient with cerebral cortical vein thrombosis

      AMERICAN JOURNAL OF HEMATOLOGY
    59. Ho, CH; Chau, WK; Hsu, HC; Gau, JP; Yu, TJ
      Causes of venous thrombosis in fifty Chinese patients

      AMERICAN JOURNAL OF HEMATOLOGY
    60. Voetsch, B; Damasceno, BP; Camargo, ECS; Massaro, A; Bacheschi, LA; Scaff, M; Annichino-Bizzacchi, JM; Arruda, VR
      Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults

      THROMBOSIS AND HAEMOSTASIS
    61. Zeinali, S; Duca, F; Zarbakhsh, B; Tagliabue, L; Mannucci, PM
      Thrombophilic mutations in Iran

      THROMBOSIS AND HAEMOSTASIS
    62. Renner, W; Koppel, H; Brodmann, M; Pabst, E; Schallmoser, K; Toplak, H; Wascher, TC; Pilger, E
      Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease

      THROMBOSIS AND HAEMOSTASIS
    63. Espinosa-Parrilla, Y; Navarro, G; Morell, M; Abella, E; Estivill, X; Sala, N
      Homozygosity for the protein S Heerlen allele is associated with type IPS deficiency in a thrombophilic pedigree with multiple risk factors

      THROMBOSIS AND HAEMOSTASIS
    64. Conard, J; Samama, MM
      Oral contraceptives, hormone replacement therapy and haemostasis

      CEPHALALGIA
    65. Bousser, MG; Kittner, S
      Oral contraceptives and stroke

      CEPHALALGIA
    66. Akar, N; Yilmaz, E; Akar, E; Deda, G; Sipahi, T
      Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct

      HAEMOSTASIS
    67. Reitsma, PH
      Genetic heterogeneity in hereditary thrombophilia

      HAEMOSTASIS
    68. Amitrano, L; Brancaccio, V; Guardascione, MA; Margaglione, M; Iannaccone, L; D'Andrea, G; Marmo, R; Ames, PRJ; Balzano, A
      Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis

      HEPATOLOGY
    69. Ara, JH; Rioja, RC; Rinon, C; Munoz, MSG; Caravaca, MLR; Miguel, JL
      Prevalence of genetic protrombotic factors (factor V Leiden and protrombinII20210 mutation) in glomerular nephropathies with or without thrombosis

      NEFROLOGIA
    70. Minnema, MC; Janssen, HLA; Niermeijer, P; de Man, RA
      Budd-Chiari syndrome: combination of genetic defects and the use of oral contraceptives leading to hypercoagulability

      JOURNAL OF HEPATOLOGY
    71. van Gijn, J
      Cerebral venous thrombosis: pathogenesis, presentation and prognosis

      JOURNAL OF THE ROYAL SOCIETY OF MEDICINE
    72. Hannaford, P
      Cardiovascular events associated with different combined oral contraceptives - A review of current data

      DRUG SAFETY
    73. Kearon, C; Crowther, M; Hirsh, J
      Management of patients with hereditary hypercoagulable disorders

      ANNUAL REVIEW OF MEDICINE
    74. Shen, MC; Lin, JS; Tsay, W
      Protein C and protein S deficiencies are the most important risk factors associated with thrombosis in Chinese venous thrombophilic patients in Taiwan

      THROMBOSIS RESEARCH
    75. Larsen, TB; Norgaard-Pedersen, B; Lundemose, JB; Rudiger, N; Gaustadnes, M; Brandslund, I
      Sudden infant death syndrome, childhood thrombosis, and presence of genetic risk factors for thrombosis

      THROMBOSIS RESEARCH
    76. Fujimura, H; Kawasaki, T; Sakata, T; Ariyoshi, H; Kato, H; Monden, M; Miyata, T
      Common C677T polymorphism in the methylenetetrahydrofolate reductase gene increases the risk for deep vein thrombosis in patients with predispositionof thrombophilia

      THROMBOSIS RESEARCH
    77. Meyer, M; Kutscher, G; Vogel, G
      The prothrombin nt20210 A allele as a risk factor for venous thromboembolism: Detection of heterozygous and homozygous carriers by alternative methods

      THROMBOSIS RESEARCH
    78. Akar, N; Yilmaz, E; Akar, E; Avcu, F; Yalcin, A; Cin, S
      Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thrombotic patients with and without FV1691 G-A

      THROMBOSIS RESEARCH
    79. De Stefano, V; Madonna, P; Giannino, A; Coppola, A; Cerbone, AM; Pauciullo, P; Di Minno, G
      Idiopathic Budd-Chiari syndrome in a patient with homozygous Factor V Leiden and heterozygous factor II G20210A mutations

      THROMBOSIS RESEARCH
    80. Manucci, PM
      The molecular basis of inherited thrombophilia

      VOX SANGUINIS
    81. Reshetnyak, TM; Patrushev, LI; Stukacheva, EA; Miroshnikov, AI; Tikhonova, TL; Nasonov, EL; Alekberova, ZS
      Leiden, G20210A mutations in prothrombin gene and antiphospholipid antibodies in systemic lupus erythematosus and antiphospholipid syndrome

      TERAPEVTICHESKII ARKHIV
    82. Kenet, G; Sadetzki, S; Murad, H; Martinowitz, U; Rosenberg, N; Gitel, S; Rechavi, G; Inbal, A
      Factor V leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children

      STROKE
    83. Kupferminc, MJ; Yair, D; Bornstein, NM; Lessing, JB; Elder, A
      Transient focal neurological deficits during pregnancy in carriers of inherited thrombophilia

      STROKE
    84. Longstreth, WT; Colven, RM
      Cerebral venous thrombosis and the G20210A mutation of factor II - Response

      STROKE
    85. Simons, PJ; Vanhooren, G
      Cerebral venous thrombosis and the G20210A mutation of factor II

      STROKE
    86. Bushnell, CD; Goldstein, LB
      Diagnostic testing for coagulopathies in patients with ischemic stroke

      STROKE
    87. Grip, O; Svensson, PJ; Lindgren, S
      Inflammatory bowel disease promotes venous thrombosis earlier in life

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    88. Kupferminc, MJ; Fait, G; Many, A; Gordon, D; Eldor, A; Lessing, JB
      Severe preeclampsia and high frequency of genetic thrombophilic mutations

      OBSTETRICS AND GYNECOLOGY
    89. Kyrle, PA; Minar, E; Hirschl, M; Bialonczyk, C; Stain, M; Schneider, B; Weltermann, A; Speiser, W; Lechner, K; Eichinger, S
      High plasma levels of factor VIII and the risk of recurrent venous thromboembolism.

      NEW ENGLAND JOURNAL OF MEDICINE
    90. Lanthier, S; Carmant, L; David, M; Larbrisseau, A; de Veber, G
      Stroke in children - The coexistence of multiple risk factors predicts poor outcome

      NEUROLOGY
    91. Weih, M; Junge-Hulsing, J; Mehraein, S; Ziemer, S; Einhaupl, KM
      Hereditary thrombophilias in ischemic stroke and sinus vein thrombosis: diagnostic, therapy and meta-analysis

      NERVENARZT
    92. Halliday, JL; Reddihough, D; Byron, K; Ekert, H; Ditchfield, M
      Hemiplegic cerebral palsy and the factor V Leiden mutation

      JOURNAL OF MEDICAL GENETICS
    93. Wramsby, ML; Sten-Linder, M; Bremme, K
      Primary habitual abortions are associated with high frequency of Factor V Leiden mutation

      FERTILITY AND STERILITY
    94. Romero, JMC; Miranda, MP
      Inherited thrombophilia in venous thromboembolic disease

      REVISTA CLINICA ESPANOLA
    95. Margaglione, M; Brancaccio, V; De Lucia, D; Martinelli, I; Ciampa, A; Grandone, E; Di Minno, G
      Inherited thrombophilic risk factors and venous thromboembolism - Distinctrole in peripheral deep venous thrombosis and pulmonary embolism

      CHEST
    96. Hessner, MJ; Budish, MA; Friedman, KD
      Genotyping of factor V G1691A (Leiden) without the use of PCR by invasive cleavage of oligonucleotide probes

      CLINICAL CHEMISTRY
    97. Ordonez, AJG; Carreira, JMF; Alvarez, MV; Sanchez, LM; Rodriguez, JMM; Garcia, EC
      A high factor II/factor X functional ratio is not a useful predictor of the FII G20210A gene mutation in thromboembolic patients undergoing oral anticoagulant treatment

      CLINICAL CHEMISTRY
    98. Jost, CHA; Bombeli, T; Schrimpf, C; Oechslin, E; Kiowski, W; Jenni, R
      Extensive thrombus formation in the right ventricle due to a rare combination of arrhythmogenic right ventricular cardiomyopathy and heterozygous prothrombin gene mutation G20210 A

      CARDIOLOGY
    99. Chan, DKY; Hu, G; Tao, H; Owens, D; Vun, CM; Woo, J; Chong, BH
      A comparison of polymorphism in the 3 '-untranslated region of the prothrombin gene between Chinese and Caucasians in Australia

      BRITISH JOURNAL OF HAEMATOLOGY
    100. Visanji, JM; Seargent, J; Tahri, D; Croft, SA; Makris, M; Preston, FE; Peake, IR; Daly, ME
      Influence of the-675 4G/5G dimorphism of the plasminogen activator inhibitor 1 promoter on thrombotic risk in patients with factor V Leiden

      BRITISH JOURNAL OF HAEMATOLOGY


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Documento generato il 15/08/20 alle ore 02:29:55