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La ricerca find articoli where soggetti phrase all words 'inherited thrombophilia' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 154 riferimenti
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    1. Crisan, D
      Genetic risk factors for thrombosis and pregnancy complications

      JOURNAL OF CLINICAL LIGAND ASSAY
    2. Schambeck, CM; Hinney, K; Haubitz, I; Taleghani, BM; Wahler, D; Keller, F
      Familial clustering of high factor VIII levels in patients with venous thromboembolism

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    3. Lopaciuk, S; Bykowska, K; Kwiecinski, H; Mickielewicz, A; Czlonkowska, A; Mendel, T; Kuczynska-Zardzewialy, A; Szelagowska, D; Windyga, J; Schroder, W; Herrmann, FH; Jedrzejowska, H
      Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    4. Dragoni, F; Tormene, D; Simioni, P; Arcieri, P; Avvisati, G; Girolami, A
      ProC global: A new automated screening assay for the evaluation of total function of the protein C system

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    5. Kupferminc, MJ; Fait, G; Many, A; Lessing, JB; Yair, D; Bar-Am, A; Eldor, A
      Low-molecular-weight heparin for the prevention of obstetric complicationsin women with thrombophilias

      HYPERTENSION IN PREGNANCY
    6. Isermann, B; Hendrickson, SB; Hutley, K; Wing, M; Weiler, H
      Tissue-restricted expression of thrombomodulin in the placenta rescues thrombomodulin-deficient mice from early lethality and reveals a secondary developmental block

      DEVELOPMENT
    7. Eldor, A
      Thrombophilia and its treatment in pregnancy

      JOURNAL OF THROMBOSIS AND THROMBOLYSIS
    8. Kearon, C
      Duration of anticoagulation for venous thromboembolism

      JOURNAL OF THROMBOSIS AND THROMBOLYSIS
    9. Shapiro, JM
      Venous thromboembolism in pregnancy

      JOURNAL OF INTENSIVE CARE MEDICINE
    10. Lynch, JK; Nelson, KB; Curry, CJ; Grether, JK
      Cerebrovascular disorders in children with the factor V Leiden mutation

      JOURNAL OF CHILD NEUROLOGY
    11. Subar, M
      Clinical evaluation of hypercoagulable states

      CLINICS IN GERIATRIC MEDICINE
    12. Santamaria, A; Mateo, J; Oliver, A; Menendez, B; Souto, JC; Borrell, M; Soria, JM; Tirado, I; Fontcuberta, J
      Risk of thrombosis associated with oral contraceptives of women from 97 families with inherited thrombophilia: high risk of thrombosis in carriers ofthe G20210A mutation of the prothrombin gene

      HAEMATOLOGICA
    13. 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
    14. Tirado, I; Mateo, J; Soria, JM; Oliver, A; Borrell, M; Coll, I; Vallve, C; Souto, JC; Martinez-Sanchez, E; Fontcuberta, J
      Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies

      HAEMATOLOGICA
    15. Mousa, HA; Alfirevic, Z
      Thrombophilia and adverse pregnancy outcome

      CROATIAN MEDICAL JOURNAL
    16. Faioni, EM
      Reliable estimates of plasma protein S levels: Are we getting any closer?

      THROMBOSIS AND HAEMOSTASIS
    17. Simmonds, RE; Lane, DA
      The endothelial cell protein C receptor: A candidate genetic risk factor for thrombosis

      THROMBOSIS AND HAEMOSTASIS
    18. von Kries, R; Junker, R; Oberle, D; Kosch, A; Nowak-Gottl, U
      Foetal growth restriction in children with prothrombotic risk factors

      THROMBOSIS AND HAEMOSTASIS
    19. Eldor, A
      Thrombophilia, thrombosis and pregnancy

      THROMBOSIS AND HAEMOSTASIS
    20. Sorensen, B; Nielsen, GL; Ebbesen, LS; Ingerslev, J
      Feasibility of LMW heparin prophylaxis for management of thrombophilia investigation in patients on oral anticoagulation therapy

      THROMBOSIS AND HAEMOSTASIS
    21. Scott, BT; Bovill, EG; Callas, PW; Hasstedt, SJ; Leppert, MF; Valliere, JE; Varvil, TS; Long, GL
      Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred

      THROMBOSIS AND HAEMOSTASIS
    22. Toulon, P; Adda, R; Perez, P
      Sensitivity of the ProC((R)) global assay for protein C pathway abnormalities. Clinical experience in 899 unselected patients with venous thromboembolism

      THROMBOSIS RESEARCH
    23. Knoll, B; Hach-Wunderle, V; Rieger, S; Haring, D; Mannhalter, C
      Combined occurrence of a heterozygous missense mutation in the protein C gene and allelic exclusion of one protein S allele leading to severe venous thrombosis

      THROMBOSIS RESEARCH
    24. Bonduel, M; Hepner, M; Sciuccati, G; Torres, AF; Tenembaum, S
      Prothrombotic disorders in children with Moyamoya syndrome

      STROKE
    25. Seligsohn, U; Lubetsky, A
      Medical progress: Genetic susceptibility to venous thrombosis.

      NEW ENGLAND JOURNAL OF MEDICINE
    26. Briones, A; Nauffal, D; Villa, P; Martinez, MA; Menendez, R; Perpina, M
      Clinical manifestations and prevalence of hypercoagulable states in patients with venous thromboembolic disease

      MEDICINA CLINICA
    27. 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
    28. Beutler, E
      Discrepancies between genotype and phenotype in hematology: an important frontier

      BLOOD
    29. Mannucci, PM
      Genetic hypercoagulability: prevention suggests testing family members

      BLOOD
    30. Nowak-Gottl, U; Junker, R; Kreuz, W; von Eckardstein, A; Kosch, A; Nohe, N; Schobess, R; Ehrenforth, S
      Risk of recurrent venous thrombosis in children with combined prothrombotic risk factors

      BLOOD
    31. Corral, J; Iniesta, JA; Gonzalez-Conejero, R; Villalon, M; Vicente, V
      Polymorphisms of clotting factors modify the risk for primary intracranialhemorrhage

      BLOOD
    32. Tapon-Bretaudiere, T
      Laboratory testing for venous thromboembolism.

      TRANSFUSION CLINIQUE ET BIOLOGIQUE
    33. de Montalembert, M
      Transfusion in patients with hemoglobinopathies.

      TRANSFUSION CLINIQUE ET BIOLOGIQUE
    34. Bonduel, M; Hepner, M; Sciuccati, G; Torres, AF; Pieroni, G; Frontroth, JP
      Prothrombotic abnormalities in children with venous thromboembolism

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    35. Boyanovski, B; Russeva, M; Dobreva, G; Ganev, V; Mladenova, A; Peicheva, V; Nikolov, K; Baleva, M
      Protein C activity in patients with antiphospholipid syndrome

      JCR-JOURNAL OF CLINICAL RHEUMATOLOGY
    36. Sartori, MT; Simioni, P; Patrassi, GM; Theodoridis, P; Tormene, D; Girolami, A
      Combined heterozygous plasminogen deficiency and factor V Leiden defect inthe same kindred

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

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

      CEREBROVASCULAR DISEASES
    39. Toulon, P; Halbmeyer, WM; Hafner, G; Schmitt, Y; Randgard, B; Odpadlik, M; Van den Eynden, C; Wagner, C
      Screening for abnormalities of the protein C anticoagulant pathway using the ProC Global assay. Results of a European multicenter evaluation

      BLOOD COAGULATION & FIBRINOLYSIS
    40. Castaman, G; Tosetto, A; Cappellari, A; Ruggeri, M; Rodeghiero, F
      The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiency

      BLOOD COAGULATION & FIBRINOLYSIS
    41. Toulon, P; Perez, P
      Screening for risk factors for thrombosis using a new generation of assaysdeveloped to evaluate the functionality of the protein C anticoagulant pathway

      HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA
    42. Solymoss, S
      Risk factors for thromboembolism: pathophysiology and detection

      CANADIAN MEDICAL ASSOCIATION JOURNAL
    43. Corral, J; Gonzalez-Conejero, R; Iniesta, JA; Rivera, J; Martinez, C; Vicente, V
      The FXIII Val34Leu polymorphism in venous and arterial thromboembolism

      HAEMATOLOGICA
    44. Higgins, JR; Kaiser, T; Moses, EK; North, R; Brennecke, SP
      Prothrombin G20210A mutation: Is it associated with pre-eclampsia?

      GYNECOLOGIC AND OBSTETRIC INVESTIGATION
    45. Lensen, RPM; Bertina, RM; de Ronde, H; Vandenbroucke, JP; Rosendaal, FR
      Venous thrombotic risk in family members of unselected individuals with factor V Leiden

      THROMBOSIS AND HAEMOSTASIS
    46. 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
    47. Mannucci, PM
      Aspects of the clinical management of hereditary thrombophilia: A personalperspective

      HAEMOSTASIS
    48. Marz, W; Nauck, M; Wieland, H
      The molecular mechanisms of inherited thrombophilia

      ZEITSCHRIFT FUR KARDIOLOGIE
    49. Trillot, N; Zawadzki, C; Watel, A; Jude, B
      The G20210A transition in the prothrombin gene and venous thromboembolic disease.

      REVUE DE MEDECINE INTERNE
    50. Dahlback, B
      Blood coagulation

      LANCET
    51. De Stefano, V; Casorelli, I; Rossi, E; Zappacosta, B; Leone, G
      Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism

      SEMINARS IN THROMBOSIS AND HEMOSTASIS
    52. Sakata, T; Kario, K; Katayama, Y; Matsuyama, T; Kato, H; Miyata, T
      Studies on congenital protein C deficiency in Japanese: Prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases

      SEMINARS IN THROMBOSIS AND HEMOSTASIS
    53. Kearon, C; Crowther, M; Hirsh, J
      Management of patients with hereditary hypercoagulable disorders

      ANNUAL REVIEW OF MEDICINE
    54. Tripodi, A; Chantarangkul, V; De Stefano, V; Mannucci, P
      Alpha(2)-macroglobulin levels are high in adult patients with congenital antithrombin deficiency

      THROMBOSIS RESEARCH
    55. Genoud, V; Castanon, M; Annichino-Bizzacchi, J; Korin, J; Kordich, L
      Prevalence of three prothrombotic polymorphisms: Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina

      THROMBOSIS RESEARCH
    56. Baglin, T
      Thrombophilia testing: what do we think the tests mean and what should we do with the results?

      JOURNAL OF CLINICAL PATHOLOGY
    57. Tischer, J; Forstpointner, R; Lohse, P; Hiller, E
      Central pulmonary embolism found in prothrombin dimorphism (hereditary thrombophilia)

      INTERNIST
    58. Martinelli, I; Bucciarelli, P; Margaglione, M; De Stefano, V; Castaman, G; Mannucci, PM
      The risk of venous thromboembolism in family members with mutations in thegenes of factor V or prothrombin or both

      BRITISH JOURNAL OF HAEMATOLOGY
    59. David, M; Losonczy, H; Sas, G; Nagy, A; Kutscher, G; Meyer, M
      Identification of mutations in 15 Hungarian families with hereditary protein C deficiency

      BRITISH JOURNAL OF HAEMATOLOGY
    60. Lensen, R; Rosendaal, F; Vandenbroucke, J; Bertina, R
      Factor V Leiden: the venous thrombotic risk in thrombophilic families

      BRITISH JOURNAL OF HAEMATOLOGY
    61. Zheng, YZ; Tong, J; Do, XP; Pu, XQ; Zhou, BT
      Prevalence of methylenetetrahydrofolate reductase C677T and its association with arterial and venous thrombosis in the Chinese population

      BRITISH JOURNAL OF HAEMATOLOGY
    62. Simioni, P; Prandoni, P; Lensing, AWA; Manfrin, D; Tormene, D; Gavasso, S; Girolami, B; Sardella, C; Prins, M; Girolami, A
      Risk for subsequent venous thromboembolic complications in carriers of theprothrombin or the factor V gene mutation with a first episode of deep-vein thrombosis

      BLOOD
    63. Taylor, FB; Stearns-Kurosawa, DJ; Kurosawa, S; Ferrell, G; Chang, ACK; Laszik, Z; Kosanke, S; Peer, G; Esmon, CT
      The endothelial cell protein C receptor aids in host defense against Escherichia coli sepsis

      BLOOD
    64. Kunz, G; Ireland, HA; Stubbs, PJ; Kahan, M; Coulton, GC; Lane, DA
      Identification and characterization of a thrombomodulin gene mutation coding for an elongated protein with reduced expression in a kindred with myocardial infarction

      BLOOD
    65. Espinosa-Parrilla, Y; Yamazaki, T; Sala, N; Dahlback, B; de Frutos, PG
      Protein S secretion differences of missense mutants account for phenotypicheterogeneity

      BLOOD
    66. Stolz, E; Kemkes-Matthes, B; Potzsch, B; Hahn, M; Kraus, J; Wirbartz, A; Kaps, M
      Screening for thrombophilic risk factors among 25 German patients with cerebral venous thrombosis

      ACTA NEUROLOGICA SCANDINAVICA
    67. Marz, W; Nauck, M; Wieland, H
      The molecular mechanisms of inherited thrombophilia

      ACUTE PULMONARY EMBOLISM
    68. Toulon, P; Perez, P; Demay, Y; Dornon, O
      Screening for abnormalities of the protein C anticoagulant pathway using the protein C pathway test

      FIBRINOLYSIS & PROTEOLYSIS
    69. Jagadeeswaran, P; Sheehan, JP
      Analysis of blood coagulation in the zebrafish

      BLOOD CELLS MOLECULES AND DISEASES
    70. Wysokinski, WE; McBane, RD; Owen, WG
      Individual propensity for arterial thrombosis

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    71. Ehrenforth, S; Prondsinski, MV; Aygoren-Pursun, E; Scharrer, I; Ganser, A
      Study of the prothrombin gene 20201 GA variant in FV : Q(506) carriers in relationship to the presence or absence of juvenile venous thromboembolism

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    72. Sartori, MT; Patrassi, GM; Theodoridis, P; Danesin, C; Abati, C; Girolami, A
      Familial association of hypoplasminogenemia and heterozygous factor V deficiency

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    73. Lippi, G; Bassi, A; Brocco, G; Manzato, F; Marini, M; Guidi, G
      Lipoprotein(a) concentration is not associated with venous thromboembolismin a case control study

      HAEMATOLOGICA
    74. Vicente, V; Gonzalez-Conejero, R; Rivera, J; Corral, J
      The prothrombin gene variant 20210A in venous and arterial thromboembolism

      HAEMATOLOGICA
    75. Takahashi, T; Shinohara, K; Nawata, R; Wakiyama, M; Hamasaki, N
      A novel mutation of the protein C gene with a frameshift deletion of 3 base pair ((3380)AGG) in exon 6 in type 1 deficiency associated with arterial and venous thrombosis

      AMERICAN JOURNAL OF HEMATOLOGY
    76. Margaglione, M; D'Andrea, G; Colaizzo, D; Cappucci, G; del Popolo, A; Brancaccio, V; Ciampa, A; Grandone, E; Di Minno, G
      Coexistence of Factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism

      THROMBOSIS AND HAEMOSTASIS
    77. Tosetto, A; Missiaglia, E; Frezzato, M; Rodeghiero, F
      The VITA Project: Prothrombin G20210A mutation and venous thromboembolism in the general population

      THROMBOSIS AND HAEMOSTASIS
    78. Martinelli, I; Cattaneo, M; Taioli, E; De Stefano, V; Chiusolo, P; Mannucci, PM
      Genetic risk factors for superficial vein thrombosis

      THROMBOSIS AND HAEMOSTASIS
    79. Norlund, L; Holm, J; Zoller, B; Ohlin, AK
      The Ala(25)-Thr mutation in the thrombomodulin gene is not frequent in Swedish patients suffering from ischemic heart disease

      THROMBOSIS AND HAEMOSTASIS
    80. Liberti, G; Bertina, RM; Rosendaal, FR
      Hormonal state rather than age influences cut-off values of protein S: Reevaluation of the thrombotic risk associated with protein S deficiency

      THROMBOSIS AND HAEMOSTASIS
    81. Esmon, CT; Xu, J; Gu, JM; Qu, DF; Laszik, Z; Ferrell, G; Stearns-Kurosawa, DJ; Kurosawa, S; Taylor, FB; Esmon, NL
      Endothelial protein C receptor

      THROMBOSIS AND HAEMOSTASIS
    82. Bovill, EG; Hasstedt, SJ; Leppert, MF; Long, GL
      Hereditary thrombophilia as a model for multigenic disease

      THROMBOSIS AND HAEMOSTASIS
    83. Croft, SA; Daly, ME; Steeds, RP; Channer, KS; Samani, NJ; Hampton, KK
      The prothrombin 20210A allele and its association with myocardial infarction

      THROMBOSIS AND HAEMOSTASIS
    84. Ohlin, AK; Marlar, RA
      Thrombomodulin gene defects in families with thromboembolic disease - A report on four families

      THROMBOSIS AND HAEMOSTASIS
    85. Turkstra, F; Karemaker, R; Kuijer, PMM; Prins, MH; Buller, HR
      Is the prevalence of the factor V Leiden mutation in patients with pulmonary embolism and deep vein thrombosis really different?

      THROMBOSIS AND HAEMOSTASIS
    86. Ehrenforth, S; Junker, R; Koch, HG; Kreuz, W; Munchow, N; Scharrer, I; Nowak-Gottl, U
      Multicentre evaluation of combined prothrombotic: defects associated with thrombophilia in childhood

      EUROPEAN JOURNAL OF PEDIATRICS
    87. Conard, J; Horellou, MH; Samama, MM; Samama, RM
      Management of pregnancy in women with thrombophilia

      HAEMOSTASIS
    88. Gallistl, S; Reitinger, T; Linhart, W; Muntean, W
      The role of inherited thrombotic disorders in the etiology of Legg-Calve-Perthes disease

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    89. Hilberg, T; Moessmer, G; Hartard, M; Jeschke, D
      Clinical sciences and orthopaedics: Case report homozygous APC resistance in an elite athlete

      INTERNATIONAL JOURNAL OF SPORTS MEDICINE
    90. Mintz-Hittner, HA; Miyashiro, MJ; Knight-Nanan, DM; O'Malley, RE; Marlar, RA
      Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency

      OPHTHALMOLOGY
    91. Sakata, T; Kario, K; Katayama, Y; Matsuyama, T; Kato, H; Miyata, T
      Analysis of 45 episodes of arterial occlusive disease in Japanese patientswith congenital protein C deficiency

      THROMBOSIS RESEARCH
    92. Cattaneo, M; Chantarangkul, V; Taioli, E; Santos, JH; Tagliabue, L
      The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: Prevalence and association with factorV G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombinlevels

      THROMBOSIS RESEARCH
    93. Trillot, N; Rugeri, L; Jude, B
      Inherited thrombophilia: laboratory evaluation and therapeutic implications

      THERAPIE
    94. Rand, JH; Luong, TH
      Thrombophilias: Diagnosis and treatment of thrombophilia relating to contraception and pregnancy

      SEMINARS IN HEMATOLOGY
    95. Kalev, M; Day, T; de Water, NV; Ockelford, P
      Screening for a prothrombotic diathesis in patients attending family planning clinics

      NEW ZEALAND MEDICAL JOURNAL
    96. De Stefano, V; Martinelli, I; Mannucci, PM; Paciaroni, K; Chiusolo, P; Casorelli, I; Rossi, E; Leone, G
      The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation

      NEW ENGLAND JOURNAL OF MEDICINE
    97. Palareti, G; Legnani, C; Frascaro, M; Flamigni, C; Gammi, L; Gola, G; Fuschini, G; Coccheri, S
      Screening for activated protein C resistance before oral contraceptive treatment: A pilot study

      CONTRACEPTION
    98. Nowak-Gottl, U; Junker, R; Hartmeier, M; Koch, HG; Munchow, N; Assmann, G; von Eckardstein, A
      Increased lipoprotein(a) is an important risk factor for venous thromboembolism in childhood

      CIRCULATION
    99. Castaman, G; Tosetto, A; Ruggeri, M; Rodeghiero, F
      Pseudohomozygosity for activated protein C resistance is a risk factor forvenous thrombosis

      BRITISH JOURNAL OF HAEMATOLOGY
    100. Faioni, EM; Franchi, F; Bucciarelli, P; Margaglione, M; De Stefano, V; Castaman, G; Finazzi, G; Mannucci, PM
      Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (Factor V leiden)

      BLOOD


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Documento generato il 06/08/20 alle ore 18:59:15