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Items: 1 to 20 of 99

1.

Cerebral infarctions manifesting as neonatal seizure.

Cômert S, Vitrinel A, Akïn Y, Canturk O, Cetinkaya E, Aksoy F.

J Coll Physicians Surg Pak. 2007 Sep;17(9):574-6.

PMID:
17903413
2.

Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study.

El-Karaksy H, El-Koofy N, El-Hawary M, Mostafa A, Aziz M, El-Shabrawi M, Mohsen NA, Kotb M, El-Raziky M, El-Sonoon MA, A-Kader H.

Ann Hematol. 2004 Nov;83(11):712-5. Epub 2004 Aug 10. Erratum in: Ann Hematol. 2005 Mar;84(3):205.

PMID:
15309526
3.

Cerebral infarcts in full term neonates.

Akman I, Ozek E, Yilmaz Y, Bilgen H.

Turk J Pediatr. 2003 Apr-Jun;45(2):141-7.

4.

Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.

Kalkanoğlu HS, Coşkun T, Aydoğdu SD, Tokatli A, Gürgey A.

J Inherit Metab Dis. 2001 Jun;24(3):367-9.

PMID:
11486902
5.

Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosis.

Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, Fowler B, Seligsohn U.

N Engl J Med. 1996 Mar 21;334(12):763-8.

6.

Factor V Leiden and prothrombin gene 20210A variant in neonatal thromboembolism and in healthy neonates and adults: a study in a single center.

Atasay B, Arsan S, Günlemez A, Kemahli S, Akar N.

Pediatr Hematol Oncol. 2003 Dec;20(8):627-34.

PMID:
14578033
7.

Factor V Leiden mutation: an unrecognized cause of hemiplegic cerebral palsy, neonatal stroke, and placental thrombosis.

Thorarensen O, Ryan S, Hunter J, Younkin DP.

Ann Neurol. 1997 Sep;42(3):372-5.

PMID:
9307261
8.

Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study.

Janssen HL, Meinardi JR, Vleggaar FP, van Uum SH, Haagsma EB, van Der Meer FJ, van Hattum J, Chamuleau RA, Adang RP, Vandenbroucke JP, van Hoek B, Rosendaal FR.

Blood. 2000 Oct 1;96(7):2364-8.

9.

Different additional risk factors for cerebral infarctions associated with the factor V Leiden mutation in a family.

Vagiakou EA, Voudris KA, Dimitriou Y, Skardoutsou A, Mastroyianni S.

J Child Neurol. 2006 Oct;21(10):903-7.

PMID:
17005112
10.

Clinical outcomes of cerebral infarctions in neonates.

Yi YY, Lee JS, Jang SI, Song JS, Yang S, Kim SK, Lim KJ, Hwang IT.

Pediatr Neurol. 2011 Dec;45(6):368-72. doi: 10.1016/j.pediatrneurol.2011.09.009.

PMID:
22114997
11.

Prevalence of Stroke in Neonates Who Admitted With Seizures in Neonatal Intensive Care Unit.

Farhadi R, Alaee A, Alipour Z, Abbaskhanian A, Nakhshab M, Derakhshanfar H.

Iran J Child Neurol. 2015 Fall;9(4):41-7.

12.

Hereditary thrombophilia in elite athletes.

Hilberg T, Jeschke D, Gabriel HH.

Med Sci Sports Exerc. 2002 Feb;34(2):218-21.

PMID:
11828228
13.

Coagulation studies, factor V Leiden, and anticardiolipin antibodies in 40 cases of cerebral venous thrombosis.

Deschiens MA, Conard J, Horellou MH, Ameri A, Preter M, Chedru F, Samama MM, Bousser MG.

Stroke. 1996 Oct;27(10):1724-30.

15.

Factor V Leiden gene mutation and thrombin generation in relation to the development of acute stroke.

Catto A, Carter A, Ireland H, Bayston TA, Philippou H, Barrett J, Lane DA, Grant PJ.

Arterioscler Thromb Vasc Biol. 1995 Jun;15(6):783-5.

16.

Prothrombotic risk factors in childhood stroke and venous thrombosis.

Heller C, Becker S, Scharrer I, Kreuz W.

Eur J Pediatr. 1999 Dec;158 Suppl 3:S117-21.

PMID:
10650849
17.

Concomitant heterozygous factor V Leiden mutation and homozygous prothrombin gene variant (G20210A) in patient with cerebral venous thrombosis.

Kurkowska-Jastrzebska I, Wicha W, Dowzenko A, Vertun-Baranowska B, Pytlewski A, Bogusławska R, Członkowska A.

Med Sci Monit. 2003 May;9(5):CS41-5.

PMID:
12761462
18.

Concomitant homozygosity for the prothrombin gene variant with mild deficiency of antithrombin III in a patient with multiple hepatic infarctions: a case report.

Emmanuelle T, Husein B, Iqbal J, Macheta M, Isaacs P.

J Med Case Rep. 2010 Apr 29;4:122. doi: 10.1186/1752-1947-4-122.

19.

[Analysis of 58 neonatal cases with cerebral infarction].

Li ZH, Chen C.

Zhonghua Er Ke Za Zhi. 2013 Jan;51(1):16-20. Chinese.

PMID:
23527926
20.

Survey of factor V leiden and prothrombin gene mutations in systemic lupus erythematosus.

Topaloglu R, Akierli C, Bakkaloglu A, Aydintug O, Ozen S, Besbas N, Ozcelik T.

Clin Rheumatol. 2001;20(4):259-61.

PMID:
11529632
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