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Items: 1 to 50 of 853

1.

Cardiovascular diseases in congenital prekallikrein deficiency: comparison with other chance-associated morbidities.

Girolami A, Ferrari S, Cosi E, Girolami B.

Blood Coagul Fibrinolysis. 2018 Jul;29(5):423-428. doi: 10.1097/MBC.0000000000000735.

PMID:
29762144
2.

Prothrombin: Another Clotting Factor After FV That Is Involved Both in Bleeding and Thrombosis.

Girolami A, Cosi E, Ferrari S, Girolami B.

Clin Appl Thromb Hemost. 2018 Jan 1:1076029618770741. doi: 10.1177/1076029618770741. [Epub ahead of print]

PMID:
29690772
3.

A structure-function analysis in patients with prekallikrein deficiency.

Girolami A, Ferrari S, Cosi E, Lombardi AM.

Hematology. 2018 Jul;23(6):346-350. doi: 10.1080/10245332.2017.1405572. Epub 2017 Nov 22.

PMID:
29165051
4.

Heparin, coumarin, protein C, antithrombin, fibrinolysis and other clotting related resistances: old and new concepts in blood coagulation.

Girolami A, Cosi E, Ferrari S, Girolami B.

J Thromb Thrombolysis. 2018 Jan;45(1):135-141. doi: 10.1007/s11239-017-1559-0. Review.

PMID:
29063359
5.

Congenital FX Deficiency Rio Tercero: A New Heterozygous Missense Mutation (Cys241Gly) with a Potentiating Effect by a Polymorphism (c. 503-57C>T).

Girolami A, Minoldo S, Ferrari S, Colussi D, Lombardi AM, Guglielmone H.

Cardiovasc Hematol Disord Drug Targets. 2017;17(2):136-141. doi: 10.2174/1871529X17666170908105839.

PMID:
28891452
6.

Role of replacement therapy in the evaluation of thrombosis occurring in congenital bleeding conditions.

Girolami A, Ferrari S, Cosi E, Girolami B.

Thromb Haemost. 2017 Oct 5;117(10):2006. doi: 10.1160/TH17-04-0251. Epub 2017 Aug 10. No abstract available.

PMID:
28796273
7.

Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders.

Girolami A, Cosi E, Ferrari S, Lombardi A, Fabris F.

Clin Appl Thromb Hemost. 2018 May;24(4):560-565. doi: 10.1177/1076029617721012. Epub 2017 Aug 4.

PMID:
28774197
8.

Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.

Girolami A, Ferrari S, Cosi E, Girolami B, Lombardi AM.

Hematology. 2018 Mar;23(2):105-110. doi: 10.1080/10245332.2017.1359900. Epub 2017 Aug 1.

PMID:
28762299
9.

Bleeding manifestations in heterozygotes with prothrombin deficiency or abnormalities vs. unaffected family members as observed during a long follow-up study.

Girolami A, Santarossa C, Cosi E, Ferrari S, Lombardi AM, Girolami B.

Blood Coagul Fibrinolysis. 2017 Dec;28(8):623-626. doi: 10.1097/MBC.0000000000000648.

PMID:
28665815
10.

Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected.

Ferrari S, Lombardi AM, Putti MC, Bertomoro A, Cortella I, Barzon I, Girolami A, Fabris F.

Platelets. 2017 Sep;28(6):621-624. doi: 10.1080/09537104.2016.1267337. Epub 2017 Feb 16. No abstract available.

PMID:
28277066
11.

New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice.

Girolami A, Cosi E, Ferrari S, Lombardi AM, Girolami B.

J Thromb Thrombolysis. 2017 Jul;44(1):71-75. doi: 10.1007/s11239-017-1488-y. Review.

PMID:
28251495
12.

Bleeding manifestations in heterozygotes with congenital FVII deficiency: a comparison with unaffected family members during a long observation period.

Girolami A, Cosi E, Ferrari S, Girolami B, Lombardi AM.

Hematology. 2017 Jul;22(6):375-379. doi: 10.1080/10245332.2017.1286540. Epub 2017 Feb 8.

PMID:
28176610
13.

Factor X Friuli Coagulation Disorder: Almost 50 Years Later.

Girolami A, Cosi E, Santarossa C, Ferrari S, Girolami B, Lombardi AM.

Clin Appl Thromb Hemost. 2018 Jan;24(1):33-40. doi: 10.1177/1076029616686423. Epub 2016 Dec 29.

PMID:
28030967
14.

Prethrombotic, prothrombotic, thrombophilic states, hypercoagulable state, thrombophilia etc.: semantics should be respected even in medical papers.

Girolami A, Cosi E, Ferrari S, Lombardi AM, Girolami B.

J Thromb Thrombolysis. 2017 Apr;43(3):390-393. doi: 10.1007/s11239-016-1459-8. Review.

PMID:
27864647
15.

Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising Observations.

Girolami A, Cosi E, Santarossa C, Ferrari S, Lombardi AM.

Acta Haematol. 2016;136(2):118-22. doi: 10.1159/000445854. Epub 2016 Jul 7.

PMID:
27385629
16.

Ischemic Strokes in Congenital Bleeding Disorders: Comparison with Myocardial Infarction and other Acute Coronary Syndromes.

Girolami A, Silvia F, Elisabetta C, Edoardo P, Bruno G.

Cardiovasc Hematol Disord Drug Targets. 2016;16(1):6-12. Review.

PMID:
27305946
17.

Drug-Induced Thrombophilic or Prothrombotic States: An Underestimated Clinical Problem That Involves Both Legal and Illegal Compounds.

Girolami A, Cosi E, Tasinato V, Santarossa C, Ferrari S, Girolami B.

Clin Appl Thromb Hemost. 2017 Oct;23(7):775-785. doi: 10.1177/1076029616652724. Epub 2016 Jun 14. Review.

PMID:
27301402
18.

A forgotten or minimized head trauma, rather than a mild FVII deficiency, is the most likely cause of a subdural hematoma.

Girolami A, Ferrari S, Cosi E, Lombardi AM.

Blood Cells Mol Dis. 2016 Sep;60:73. doi: 10.1016/j.bcmd.2016.05.008. Epub 2016 May 13. No abstract available.

PMID:
27234708
19.

Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).

Girolami A, Cosi E, Santarossa C, Ferrari S, Girolami B, Lombardi AM.

Eur J Haematol. 2016 Dec;97(6):547-553. doi: 10.1111/ejh.12767. Epub 2016 May 30.

PMID:
27124643
20.

A family with factor X deficiency from Argentina: a compound heterozygosis because of the combination of a new mutation (Gln138Arg) with an already known one (Glu350Lys).

Girolami A, Molina MA, Galletti ML, Ferrari S, Sambado L, Guglielmone H.

Blood Coagul Fibrinolysis. 2016 Sep;27(6):732-6. doi: 10.1097/MBC.0000000000000563.

PMID:
27031279
21.

Congenital factor XI and factor VII deficiencies assure an apparent opposite protection against arterial or venous thrombosis: An intriguing observation.

Girolami A, Peroni E, Girolami B, Ferrari S, Lombardi AM.

Hematology. 2016 Sep;21(8):486-9. doi: 10.1080/10245332.2015.1112495. Epub 2016 Feb 17.

PMID:
26872273
22.

Pulmonary embolism in congenital bleeding disorders: intriguing discrepancies among different clotting factors deficiencies.

Girolami A, Cosi E, Tasinato V, Peroni E, Girolami B, Lombardi AM.

Blood Coagul Fibrinolysis. 2016 Jul;27(5):517-25. doi: 10.1097/MBC.0000000000000437. Review.

PMID:
26829362
23.

Acquired Isolated FVII Deficiency: An Underestimated and Potentially Important Laboratory Finding.

Girolami A, Santarossa C, Cosi E, Ferrari S, Lombardi AM.

Clin Appl Thromb Hemost. 2016 Nov;22(8):705-711. Epub 2015 Aug 31. Review.

PMID:
26329909
24.

The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VII.

Girolami A, Cosi E, Santarossa C, Ferrari S, Luigia Randi M.

Semin Thromb Hemost. 2015 Jun;41(4):366-73. doi: 10.1055/s-0035-1549851. Epub 2015 May 14. Review.

PMID:
25973586
25.

Prevalence of hypertension and its complications in congenital prekallikrein deficiency: analysis of all reported cases and clinical significance.

Girolami A, Ferrari S, Cosi E, Sambado L, Girolami B.

Blood Coagul Fibrinolysis. 2015 Jul;26(5):560-3. doi: 10.1097/MBC.0000000000000294.

PMID:
25886833
26.

Complex history of the discovery and characterization of congenital factor X deficiency.

Girolami A, Cosi E, Sambado L, Girolami B, Randi ML.

Semin Thromb Hemost. 2015 Jun;41(4):359-65. doi: 10.1055/s-0034-1544000. Epub 2015 Apr 14. Review.

PMID:
25875733
27.

Venous thrombosis in von Willebrand disease as observed in one centre and as reported in the literature.

Girolami A, Tasinato V, Sambado L, Peroni E, Casonato A.

Blood Coagul Fibrinolysis. 2015 Jan;26(1):54-8. doi: 10.1097/MBC.0000000000000179.

PMID:
25158987
28.

Myocardial infarctions and other acute coronary syndromes in rare congenital bleeding disorders: a critical analysis of all reported cases.

Girolami A, Ferrari S, Sambado L, Peroni E, Cosi E.

Clin Appl Thromb Hemost. 2015 May;21(4):359-64. doi: 10.1177/1076029614548056. Epub 2014 Aug 25. Review.

PMID:
25155499
29.

The old and the new in prekallikrein deficiency: historical context and a family from Argentina with PK deficiency due to a new mutation (Arg541Gln) in exon 14 associated with a common polymorphysm (Asn124Ser) in exon 5.

Girolami A, Vidal J, Sabagh M, Gervan N, Parody M, Peroni E, Sambado L, Guglielmone H.

Semin Thromb Hemost. 2014 Jul;40(5):592-9. doi: 10.1055/s-0034-1384767. Epub 2014 Jul 30. Erratum in: Semin Thromb Hemost. 2014 Sep;40(6):712. Salagh, Marcela [corrected to Sabagh, Marcela].

PMID:
25075649
31.

Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease.

Pontara E, Gresele P, Cattini MG, Daidone V, Barbon G, Girolami A, Zanon E, Casonato A.

Blood Coagul Fibrinolysis. 2014 Jun;25(4):401-4. doi: 10.1097/MBC.0000000000000067.

PMID:
24418945
32.

Pathogenetic role of Factor VII deficiency and thrombosis in cross-reactive material positive patients.

Girolami A, Sambado L, Bonamigo E, Ferrari S, Lombardi AM.

Lab Hematol. 2013 Dec;19(4):17-21. doi: 10.1532/LH96.12011.

PMID:
24370871
33.

Venous thrombosis in rare or unusual sites: a diagnostic challenge.

Girolami A, Treleani M, Bonamigo E, Tasinato V, Girolami B.

Semin Thromb Hemost. 2014 Feb;40(1):81-7. doi: 10.1055/s-0033-1363471. Epub 2013 Dec 17. Review.

PMID:
24347377
34.

Timely care for frail older people referred to hospital improves efficiency and reduces mortality without the need for extra resources.

Silvester KM, Mohammed MA, Harriman P, Girolami A, Downes TW.

Age Ageing. 2014 Jul;43(4):472-7. doi: 10.1093/ageing/aft170. Epub 2013 Nov 12.

PMID:
24222658
35.

Bleeding manifestations apparently unrelated to coagulation or other organic disorders: A tentative classification and diagnostic clues.

Girolami A, Bertozzi I, Tasinato V, Sambado L, Treleani M.

Hematology. 2014 Jul;19(5):293-8. doi: 10.1179/1607845413Y.0000000133. Epub 2013 Nov 25.

PMID:
24164712
36.

Eating quality of beef from free-range and confined Podolian young bulls.

Braghieri A, Pacelli C, Piazzolla N, Girolami A, Napolitano F.

J Anim Sci. 2013 Dec;91(12):5885-93. doi: 10.2527/jas.2012-6220. Epub 2013 Oct 14.

PMID:
24126271
37.

A family with factor-XI deficiency due to a compound heterozygosis between Gln 47 Pro (new mutation) in exon 3 and Leu 619 Pro in exon 15.

Girolami A, Sambado L, Peroni E, Santarossa L, Lombardi AM.

Blood Coagul Fibrinolysis. 2014 Mar;25(2):191-5. doi: 10.1097/MBC.0b013e3283641935.

PMID:
24121361
38.

Image analysis with the computer vision system and the consumer test in evaluating the appearance of Lucanian dry sausage.

Girolami A, Napolitano F, Faraone D, Di Bello G, Braghieri A.

Meat Sci. 2014 Jan;96(1):610-6. doi: 10.1016/j.meatsci.2013.08.006. Epub 2013 Aug 15.

PMID:
24041911
39.

Congenital Thrombophilia and Intracardiac Thrombosis: Probably an Underdiagnosed Event.

Girolami A, de Marinis GB, Treleani M, Tasinato V, Girolami B.

Cardiol Res. 2013 Jun;4(3):109-115. doi: 10.4021/cr278e. Epub 2013 Jul 11.

40.

Discrepant ratios of arterial versus venous thrombosis in hemophilia A as compared with hemophilia B.

Girolami A, Bertozzi I, de Marinis GB, Tasinato V, Sambado L.

J Thromb Thrombolysis. 2014 Apr;37(3):293-7. doi: 10.1007/s11239-013-0943-7.

PMID:
23681676
41.

Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiency.

Girolami A, Berti de Marinis G, Bertozzi I, Peroni E, Tasinato V, Lombardi AM.

Eur J Haematol. 2013 Aug;91(2):152-6. doi: 10.1111/ejh.12129. Epub 2013 May 24.

PMID:
23621110
42.

Consumer preference for chicken breast may be more affected by information on organic production than by product sensory properties.

Napolitano F, Castellini C, Naspetti S, Piasentier E, Girolami A, Braghieri A.

Poult Sci. 2013 Mar;92(3):820-6. doi: 10.3382/ps.2012-02633.

PMID:
23436534
43.

Homozygous FVII deficiencies with different reactivity towards tissue thromboplastins of different origin.

Girolami A, Scarparo P, Bonamigo E, Treleani M, Lombardi AM.

Hematology. 2012 Nov;17(6):350-4. doi: 10.1179/1024533212Z.000000000144.

PMID:
23168073
44.

A comment about the correct attribution of the discovery of FX Friuli disorder.

Girolami A, Bonamigo E.

Clin Appl Thromb Hemost. 2012 Nov;18(6):668-9. doi: 10.1177/1076029612448420. No abstract available.

PMID:
23129784
45.

The impact of blood coagulability on atherosclerosis and cardiovascular disease: a rebuttal.

Girolami A, Sambado L, Lombardi AM.

J Thromb Haemost. 2013 Jan;11(1):213-4; discussion 215-6. doi: 10.1111/jth.12030. No abstract available.

46.

Occurrence of thrombosis in congenital thrombocytopenic disorders: a critical annotation of the literature.

Girolami A, Sambado L, Bonamigo E, Vettore S, Lombardi AM.

Blood Coagul Fibrinolysis. 2013 Jan;24(1):18-22. doi: 10.1097/MBC.0b013e3283597634. Review.

PMID:
23037321
47.

Measurement of meat color using a computer vision system.

Girolami A, Napolitano F, Faraone D, Braghieri A.

Meat Sci. 2013 Jan;93(1):111-8. doi: 10.1016/j.meatsci.2012.08.010. Epub 2012 Aug 17.

PMID:
22981646
48.

Recombinant FVIIa concentrate-associated thrombotic events in congenital bleeding disorders other than hemophilias.

Girolami A, de Marinis GB, Bonamigo E, Lombardi AM.

Hematology. 2012 Nov;17(6):346-9. doi: 10.1179/1607845412Y.0000000027. Epub 2012 Sep 12.

PMID:
22980722
49.

Arterial and venous thromboses in patients with idiopathic (immunological) thrombocytopenia: a possible contributing role of cortisone-induced hypercoagulable state.

Girolami A, de Marinis GB, Bonamigo E, Treleani M, Vettore S.

Clin Appl Thromb Hemost. 2013 Nov-Dec;19(6):613-8. doi: 10.1177/1076029612452114. Epub 2012 Jul 12.

PMID:
22790661
50.

Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard-Soulier syndrome.

Girolami A, Vettore S, Vianello F, Berti de Marinis G, Fabris F.

J Thromb Thrombolysis. 2012 Nov;34(4):513-7. doi: 10.1007/s11239-012-0742-6.

PMID:
22569901

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