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Items: 1 to 20 of 1168

1.

Physical activity participation and bleeding characteristics in young patients with severe haemophilia.

Tiktinsky R, Kenet G, Dvir Z, Falk B, Heim M, Martinowitz U, Katz-Leurer M.

Haemophilia. 2009 May;15(3):695-700. doi: 10.1111/j.1365-2516.2009.01990.x. Epub 2008 Feb 27.

PMID:
19298376
2.

Von Willebrand disease and recurrent hematoperitoneum due to the rupture of haemorrhagic ovarian cysts.

Radakovic B, Grgic O.

Haemophilia. 2009 Mar;15(2):607-9. doi: 10.1111/j.1365-2516.2008.01930.x. Epub 2008 Feb 1. No abstract available.

PMID:
19187196
3.

Association von Willebrand's disease and nevoid basal cell carcinoma syndrome (Gorlin syndrome).

Gallego L, Junquera L.

Haemophilia. 2008 Jul;14(4):835-7. No abstract available.

PMID:
19160467
4.

Long-term prophylaxis in severe haemophilia seems to preserve bone mineral density.

Khawaji M, Akesson K, Berntorp E.

Haemophilia. 2009 Jan;15(1):261-6. doi: 10.1111/j.1365-2516.2008.01912.x. Epub 2008 Nov 3.

PMID:
19149852
5.

Hereditary haemorrhagic telangiectasia.

Sharathkumar AA, Shapiro A.

Haemophilia. 2008 Nov;14(6):1269-80. doi: 10.1111/j.1365-2516.2008.01774.x. Review.

PMID:
19141168
6.

Plasminogen deficiency.

Mehta R, Shapiro AD.

Haemophilia. 2008 Nov;14(6):1261-8. doi: 10.1111/j.1365-2516.2008.01825.x. Review.

PMID:
19141167
7.

Plasminogen activator inhibitor type 1 deficiency.

Mehta R, Shapiro AD.

Haemophilia. 2008 Nov;14(6):1255-60. doi: 10.1111/j.1365-2516.2008.01834.x. Review.

PMID:
19141166
8.

Alpha2-antiplasmin and its deficiency: fibrinolysis out of balance.

Carpenter SL, Mathew P.

Haemophilia. 2008 Nov;14(6):1250-4. doi: 10.1111/j.1365-2516.2008.01766.x. Review.

PMID:
19141165
9.

Platelet function defects.

Simon D, Kunicki T, Nugent D.

Haemophilia. 2008 Nov;14(6):1240-9. doi: 10.1111/j.1365-2516.2008.01898.x.

PMID:
19141164
10.

Inherited antithrombin deficiency: a review.

Patnaik MM, Moll S.

Haemophilia. 2008 Nov;14(6):1229-39. doi: 10.1111/j.1365-2516.2008.01830.x. Review.

PMID:
19141163
11.

Protein C deficiency.

Goldenberg NA, Manco-Johnson MJ.

Haemophilia. 2008 Nov;14(6):1214-21. doi: 10.1111/j.1365-2516.2008.01838.x.

PMID:
19141162
12.

Familial deficiency of vitamin K-dependent clotting factors.

Weston BW, Monahan PE.

Haemophilia. 2008 Nov;14(6):1209-13. doi: 10.1111/j.1365-2516.2008.01853.x.

13.

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
14.

Factor XIII deficiency.

Hsieh L, Nugent D.

Haemophilia. 2008 Nov;14(6):1190-200. doi: 10.1111/j.1365-2516.2008.01857.x. Review.

PMID:
19141159
15.

Diagnosis and treatment of inherited factor X deficiency.

Brown DL, Kouides PA.

Haemophilia. 2008 Nov;14(6):1176-82. doi: 10.1111/j.1365-2516.2008.01856.x.

PMID:
19141158
16.

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
17.

Factor V deficiency: a concise review.

Huang JN, Koerper MA.

Haemophilia. 2008 Nov;14(6):1164-9. doi: 10.1111/j.1365-2516.2008.01785.x. Review.

PMID:
19141156
18.

Abnormalities of prothrombin: a review of the pathophysiology, diagnosis, and treatment.

Meeks SL, Abshire TC.

Haemophilia. 2008 Nov;14(6):1159-63. doi: 10.1111/j.1365-2516.2008.01832.x. Review.

PMID:
19141155
19.

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
20.

Prevention of haemophilic arthropathy during childhood. May common orthopaedic management be extrapolated from patients without inhibitors to patients with inhibitors?

Rodriguez-Merchan EC, Hedner U, Heijnen L, Jimenez-Yuste V, Lee CA, Morfini M, Querol F, Roosendaal G, Santagostino E, Solimeno LP.

Haemophilia. 2008 Nov;14 Suppl 6:68-81. doi: 10.1111/j.1365-2516.2008.01892.x.

PMID:
19134036

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