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Results: 1 to 20 of 94

Similar articles for PubMed (Select 23097990)

1.

[The mutation of genes of hemostasis system in patients with venous cerebral angiodystonia against the background of connective tissue dysplasia].

Kotovshchikova EF, Buevich EI, Pen'kova EV, Kulikov VP, Chudimov VF, Siul'zhina EN, Bogdanova IV, Bochkarev AP.

Klin Lab Diagn. 2012 Aug;(8):33-6. Russian.

PMID:
23097990
2.

Propensity for hemorrhage and thrombosis in chronic myeloproliferative disorders.

Kessler CM.

Semin Hematol. 2004 Apr;41(2 Suppl 3):10-4. Review.

PMID:
15190517
3.

Inherited bleeding disorders.

Blanchette VS, Sparling C, Turner C.

Baillieres Clin Haematol. 1991 Apr;4(2):291-332. Review.

PMID:
1912663
4.
5.

[Physiologic blood coagulation studies in idiopathic arterial thrombosis].

Nowak-Göttl U, Kreuz WD, Krackhardt B, Freund H, Funk M, Linde R, Jacobi G, Scharrer I.

Monatsschr Kinderheilkd. 1992 Mar;140(3):183-7. German.

PMID:
1603102
6.
7.

[Coagulation factor mutations and thrombosis].

Aiach M, Alhenc-Gelas M, Borgel D, Emmerich J, Gandrille S, Picard V.

Med Sci (Paris). 2006 Nov;22(11):985-9. Review. French.

8.

A comprehensive study on hemostasis in CAPD patients treated with erythropoietin.

Malyszko J, Suchowierska E, Malyszko JS, Mysliwiec M.

Perit Dial Int. 2002 Sep-Oct;22(5):582-92.

9.
10.

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.

PMID:
22321862
11.

Disorders of platelet function: mechanisms, diagnosis and management.

Huebsch LB, Harker LA.

West J Med. 1981 Feb;134(2):109-27. Review.

12.

Tissue factor: (patho)physiology and cellular biology.

Eilertsen KE, Østerud B.

Blood Coagul Fibrinolysis. 2004 Oct;15(7):521-38. Review.

PMID:
15389118
13.

[The syndrome of undifferentiated dysplasia of the connective tissue].

Pizova NV, Dmitriev AN, Druzhinin DS, Chizhov PA, Tabakov V.

Zh Nevrol Psikhiatr Im S S Korsakova. 2012;112(6):4-7. Russian. No abstract available.

PMID:
22983225
14.

[Non-invasive methods for the assessment of platelet, leukocyte, erythrocyte aggregation and coagulation hemostasis].

Kuznik BI, Faĭn IA, Kaminskiĭ AV, Maksimova OG, Kustovskaia EM, Martynova EN, Rodnina OS, Khasanova NV.

Klin Med (Mosk). 2013;91(8):57-60. Russian.

PMID:
24437188
15.

Milestones and perspectives in coagulation and hemostasis.

Lippi G, Favaloro EJ, Franchini M, Guidi GC.

Semin Thromb Hemost. 2009 Feb;35(1):9-22. doi: 10.1055/s-0029-1214144. Epub 2009 Mar 23. Review.

PMID:
19308889
17.

Modifier genes for disorders of thrombosis and hemostasis.

Westrick RJ, Ginsburg D.

J Thromb Haemost. 2009 Jul;7 Suppl 1:132-5. doi: 10.1111/j.1538-7836.2009.03362.x. Review.

PMID:
19630785
18.

Haemostatic changes and the oral contraceptive pill.

Norris LA, Bonnar J.

Baillieres Clin Obstet Gynaecol. 1997 Sep;11(3):545-64. Review.

PMID:
9488791
19.

[Changes in hemostasis system in patients with hereditary thrombophilia caused by mutation of blood coagulation factor V ( factor V Leiden)].

Papaian LP, Kobilianskaia VA, Sheĭdina AM, Baranovskaia SS, Sirotkina OV, Kargin VD, Saltykova NB, Beliazo OE, Golovina OG, Papaian KA, Tarkovskaia LR.

Ter Arkh. 2001;73(7):47-51. Russian.

PMID:
11523408
20.
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