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Results: 1 to 20 of 264

1.

Research in haemophilia B - approaching the request for high evidence levels in a rare disease.

Berger K, Schopohl D, Hilger A, Behr Gross ME, Giangrande P, Peyvandi F, Seitz R, Schramm W.

Haemophilia. 2014 Dec 11. doi: 10.1111/hae.12603. [Epub ahead of print]

PMID:
25495927
[PubMed - as supplied by publisher]
2.

Pregnancy complications in acquired thrombotic thrombocytopenic purpura: a case¿control study.

Ferrari B, Maino A, Lotta LA, Artoni A, Pontiggia S, Trisolini SM, Malato A, Rosendaal FR, Peyvandi F.

Orphanet J Rare Dis. 2014 Nov 28;9(1):193. [Epub ahead of print]

PMID:
25431165
[PubMed - as supplied by publisher]
Free Article
3.

Management of pregnancy in type 2B von Willebrand disease: case report and literature review.

Biguzzi E, Siboni SM, Ossola MW, Zaina B, Migliorini AC, Peyvandi F.

Haemophilia. 2014 Nov 27. doi: 10.1111/hae.12580. [Epub ahead of print] No abstract available.

PMID:
25431025
[PubMed - as supplied by publisher]
4.

Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency.

Asselta R, Platé M, Robusto M, Borhany M, Guella I, Soldà G, Afrasiabi A, Menegatti M, Shamsi T, Peyvandi F, Duga S.

Thromb Haemost. 2014 Nov 27;113(2). [Epub ahead of print]

PMID:
25427968
[PubMed - as supplied by publisher]
5.

Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levels.

Bucciarelli P, Siboni SM, Stufano F, Biguzzi E, Canciani MT, Baronciani L, Pagliari MT, La Marca S, Mistretta C, Rosendaal FR, Peyvandi F.

J Thromb Haemost. 2014 Nov 26. doi: 10.1111/jth.12799. [Epub ahead of print]

PMID:
25425019
[PubMed - as supplied by publisher]
6.

A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity.

Rossio R, Lotta LA, Pontiggia S, Borsa Ghiringhelli N, Garagiola I, Ardissino G, Mikovic D, Cugno M, Peyvandi F.

Haematologica. 2014 Nov 7. pii: haematol.2014.111062. [Epub ahead of print]

PMID:
25381125
[PubMed - as supplied by publisher]
Free Article
7.

Congenital and acquired ADAMTS13 deficiency: Two mechanisms, one patient.

Ferrari B, Cairo A, Pontiggia S, Mancini I, Masini L, Peyvandi F.

J Clin Apher. 2014 Nov 4. doi: 10.1002/jca.21366. [Epub ahead of print]

PMID:
25367325
[PubMed - as supplied by publisher]
8.

Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.

Biguzzi E, Franchi F, Acaia B, Ossola W, Nava U, Paraboschi EM, Asselta R, Peyvandi F.

Haemophilia. 2014 Nov;20(6):e377-83. doi: 10.1111/hae.12514. Epub 2014 Oct 21.

PMID:
25333208
[PubMed - in process]
9.

A two-step approach (Enzyme-linked immunosorbent assay and confirmation assay) to detect antibodies against von Willebrand factor in patients with Acquired von Willebrand Syndrome.

Franchi F, Biguzzi E, Stufano F, Siboni SM, Baronciani L, Peyvandi F.

Thromb Res. 2014 Dec;134(6):1316-22. doi: 10.1016/j.thromres.2014.09.020. Epub 2014 Sep 28.

PMID:
25300810
[PubMed - in process]
10.

How the direct oral anticoagulant apixaban affects hemostatic parameters. Results of a multicenter multiplatform study.

Tripodi A, Padovan L, Testa S, Legnani C, Chantarangkul V, Scalambrino E, Ludovici S, Bassi L, Peyvandi F.

Clin Chem Lab Med. 2014 Aug 7. pii: /j/cclm.ahead-of-print/cclm-2014-0531/cclm-2014-0531.xml. doi: 10.1515/cclm-2014-0531. [Epub ahead of print]

PMID:
25153405
[PubMed - as supplied by publisher]
11.

Salvage therapy with high dose Intravenous Immunoglobulins in acquired Von Willebrand Syndrome and unresponsive severe intestinal bleeding.

Cugno M, Tedeschi A, Siboni SM, Stufano F, Depetri F, Franchi F, Griffini S, Peyvandi F.

Exp Hematol Oncol. 2014 Jun 4;3:15. doi: 10.1186/2162-3619-3-15. eCollection 2014.

PMID:
24926417
[PubMed]
Free PMC Article
12.

The European Haemophilia Network (EUHANET).

Makris M, Calizzani G, Fischer K, Gatt A, Gilman E, Hollingsworth R, Lambert T, Lassila R, Mannucci PM, Peyvandi F, Windyga J.

Blood Transfus. 2014 Apr;12 Suppl 3:s515-8. doi: 10.2450/2014.0008-14s. No abstract available.

PMID:
24922291
[PubMed - in process]
Free PMC Article
13.

Does the orphan medicinal product regulation assist or hinder access to innovative haemophilia treatment in Europe?

O'Mahony B, Peyvandi F, Bok A.

Haemophilia. 2014 Jul;20(4):455-8. doi: 10.1111/hae.12462. Epub 2014 May 8. No abstract available.

PMID:
24805888
[PubMed - in process]
14.

Reply to: The importance and challenge of pediatric trials of hemophilia drugs.

Peyvandi F, Rosendaal FR, O'Mahony B, Mannucci PM.

Nat Med. 2014 May;20(5):466. doi: 10.1038/nm.3551. No abstract available.

PMID:
24804749
[PubMed - indexed for MEDLINE]
15.

The bleeding score predicts clinical outcomes and replacement therapy in adults with von Willebrand disease.

Federici AB, Bucciarelli P, Castaman G, Mazzucconi MG, Morfini M, Rocino A, Schiavoni M, Peyvandi F, Rodeghiero F, Mannucci PM.

Blood. 2014 Jun 26;123(26):4037-44. doi: 10.1182/blood-2014-02-557264. Epub 2014 Apr 30.

PMID:
24786773
[PubMed - indexed for MEDLINE]
16.

Joint WFH-ISTH session: issues in clinical trial design.

Peyvandi F, Farrugia A, Iorio A, Key NS, Srivastava A.

Haemophilia. 2014 May;20 Suppl 4:137-44. doi: 10.1111/hae.12415. Review.

PMID:
24762289
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
24762279
[PubMed - indexed for MEDLINE]
18.

FRETS-VWF73 rather than CBA assay reflects ADAMTS13 proteolytic activity in acquired thrombotic thrombocytopenic purpura patients.

Mancini I, Valsecchi C, Lotta LA, Deforche L, Pontiggia S, Bajetta M, Palla R, Vanhoorelbeke K, Peyvandi F.

Thromb Haemost. 2014 Aug;112(2):297-303. doi: 10.1160/TH13-08-0688. Epub 2014 Apr 17.

PMID:
24740645
[PubMed - in process]
19.

Assaying FVIII activity: one method is not enough, and never was.

Makris M, Peyvandi F.

Haemophilia. 2014 May;20(3):301-3. doi: 10.1111/hae.12446. No abstract available.

PMID:
24731127
[PubMed - in process]
20.

Thrombin generation in patients with idiopathic sudden sensorineural hearing loss.

Tripodi A, Capaccio P, Pignataro L, Chantarangkul V, Menegatti M, Bamonti F, Clerici M, De Giuseppe R, Peyvandi F.

Thromb Res. 2014 Jun;133(6):1130-4. doi: 10.1016/j.thromres.2014.03.031. Epub 2014 Mar 21.

PMID:
24690481
[PubMed - in process]

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