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Items: 1 to 20 of 117

1.

Rare bleeding disorders.

Peyvandi F, Bolton-Maggs PH, Batorova A, De Moerloose P.

Haemophilia. 2012 Jul;18 Suppl 4:148-53. doi: 10.1111/j.1365-2516.2012.02841.x. Review.

PMID:
22726099
2.

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders.

Peyvandi F, Palla R, Menegatti M, Siboni SM, Halimeh S, Faeser B, Pergantou H, Platokouki H, Giangrande P, Peerlinck K, Celkan T, Ozdemir N, Bidlingmaier C, Ingerslev J, Giansily-Blaizot M, Schved JF, Gilmore R, Gadisseur A, Benedik-Dolničar M, Kitanovski L, Mikovic D, Musallam KM, Rosendaal FR; European Network of Rare Bleeding Disorders Group.

J Thromb Haemost. 2012 Apr;10(4):615-21. doi: 10.1111/j.1538-7836.2012.04653.x.

3.

Combined FV and FVIII deficiency.

Spreafico M, Peyvandi F.

Haemophilia. 2008 Nov;14(6):1201-8. doi: 10.1111/j.1365-2516.2008.01845.x. Review.

PMID:
19141160
4.

Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management.

Peyvandi F, Palla R, Menegatti M, Mannucci PM.

Semin Thromb Hemost. 2009 Jun;35(4):349-55. doi: 10.1055/s-0029-1225757. Epub 2009 Jul 13.

PMID:
19598063
5.

Rare bleeding disorders.

Peyvandi F, Cattaneo M, Inbal A, De Moerloose P, Spreafico M.

Haemophilia. 2008 Jul;14 Suppl 3:202-10. doi: 10.1111/j.1365-2516.2008.01751.x. Review.

PMID:
18510543
6.

Rare bleeding disorders - bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency.

James P, Salomon O, Mikovic D, Peyvandi F.

Haemophilia. 2014 May;20 Suppl 4:71-5. doi: 10.1111/hae.12402. Review.

7.

Rare bleeding disorders.

Peyvandi F, Kaufman RJ, Seligsohn U, Salomon O, Bolton-Maggs PH, Spreafico M, Menegatti M, Palla R, Siboni S, Mannucci PM.

Haemophilia. 2006 Jul;12 Suppl 3:137-42. Review.

PMID:
16684009
8.

Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias.

Acharya SS, Coughlin A, Dimichele DM; North American Rare Bleeding Disorder Study Group.

J Thromb Haemost. 2004 Feb;2(2):248-56.

9.

Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India.

Viswabandya A, Baidya S, Nair SC, Abraham A, George B, Mathews V, Chandy M, Srivastava A.

Haemophilia. 2012 May;18(3):e195-200. doi: 10.1111/j.1365-2516.2011.02730.x. Epub 2012 Jan 4.

PMID:
22221743
10.

Factor VII deficiency: defining the clinical picture and optimizing therapeutic options.

Lapecorella M, Mariani G; International Registry on Congenital Factor VII Deficiency.

Haemophilia. 2008 Nov;14(6):1170-5. doi: 10.1111/j.1365-2516.2008.01844.x. Review.

PMID:
19141157
11.

Thrombosis in rare bleeding disorders.

Ruiz-Sáez A.

Hematology. 2012 Apr;17 Suppl 1:S156-8. doi: 10.1179/102453312X13336169156690.

PMID:
22507808
12.

Rare coagulation disorders: fibrinogen, factor VII and factor XIII.

de Moerloose P, Schved JF, Nugent D.

Haemophilia. 2016 Jul;22 Suppl 5:61-5. doi: 10.1111/hae.12965.

PMID:
27405678
13.

Rare bleeding disorders: worldwide efforts for classification, diagnosis, and management.

Peyvandi F, Menegatti M, Palla R.

Semin Thromb Hemost. 2013 Sep;39(6):579-84. doi: 10.1055/s-0033-1349221. Epub 2013 Jul 25. Review.

PMID:
23888434
14.

Occurrence of thrombosis in rare bleeding disorders.

Ruiz-Saez A.

Semin Thromb Hemost. 2013 Sep;39(6):684-92. doi: 10.1055/s-0033-1353391. Epub 2013 Aug 8. Review.

PMID:
23929306
15.

Factor XI deficiency.

Gomez K, Bolton-Maggs P.

Haemophilia. 2008 Nov;14(6):1183-9. doi: 10.1111/j.1365-2516.2008.01667.x. Epub 2008 Feb 27. Review.

PMID:
18312365
16.

Solvent/detergent plasma for prevention of bleeding in recessively inherited coagulation disorders: dosing, pharmacokinetics and clinical efficacy.

Santagostino E, Mancuso ME, Morfini M, Schiavoni M, Tagliaferri A, Barillari G, Mannucci PM.

Haematologica. 2006 May;91(5):634-9.

17.

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation.

Bolton-Maggs PH, Perry DJ, Chalmers EA, Parapia LA, Wilde JT, Williams MD, Collins PW, Kitchen S, Dolan G, Mumford AD.

Haemophilia. 2004 Sep;10(5):593-628. Review.

PMID:
15357789
18.

The use of desmopressin in congenital factor XI deficiency: a systematic review.

Franchini M, Manzato F, Salvagno GL, Montagnana M, Lippi G.

Ann Hematol. 2009 Oct;88(10):931-5. doi: 10.1007/s00277-009-0792-9. Epub 2009 Jul 17. Review.

PMID:
19609524
19.

Treatment of congenital fibrinogen deficiency: overview and recent findings.

Tziomalos K, Vakalopoulou S, Perifanis V, Garipidou V.

Vasc Health Risk Manag. 2009;5:843-8. Epub 2009 Oct 12. Review.

20.

Rare inherited disorders of fibrinogen.

Acharya SS, Dimichele DM.

Haemophilia. 2008 Nov;14(6):1151-8. doi: 10.1111/j.1365-2516.2008.01831.x. Review.

PMID:
19141154
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