172 related articles for article (PubMed ID: 12208918)
1. Prospective reevaluation of the association between thrombotic diathesis and legg-perthes disease.
Hresko MT; McDougall PA; Gorlin JB; Vamvakas EC; Kasser JR; Neufeld EJ
J Bone Joint Surg Am; 2002 Sep; 84(9):1613-8. PubMed ID: 12208918
[TBL] [Abstract][Full Text] [Related]
2. Legg-Calve-Perthes disease and thrombophilia.
Balasa VV; Gruppo RA; Glueck CJ; Wang P; Roy DR; Wall EJ; Mehlman CT; Crawford AH
J Bone Joint Surg Am; 2004 Dec; 86(12):2642-7. PubMed ID: 15590848
[TBL] [Abstract][Full Text] [Related]
3. Coagulation abnormalities in Legg-Calvé-Perthes disease.
Vosmaer A; Pereira RR; Koenderman JS; Rosendaal FR; Cannegieter SC
J Bone Joint Surg Am; 2010 Jan; 92(1):121-8. PubMed ID: 20048104
[TBL] [Abstract][Full Text] [Related]
4. Legg-perthes disease and heritable thrombophilia.
López-Franco M; González-Morán G; De Lucas JC; Llamas P; de Velasco JF; Vivancos JC; Epeldegui-Torre T
J Pediatr Orthop; 2005; 25(4):456-9. PubMed ID: 15958894
[TBL] [Abstract][Full Text] [Related]
5. The role of protein C, protein S, and resistance to activated protein C in Legg-Perthes disease.
Eldridge J; Dilley A; Austin H; EL-Jamil M; Wolstein L; Doris J; Hooper WC; Meehan PL; Evatt B
Pediatrics; 2001 Jun; 107(6):1329-34. PubMed ID: 11389252
[TBL] [Abstract][Full Text] [Related]
6. The role of inherited thrombotic disorders in the etiology of Legg-Calvé-Perthes disease.
Gallistl S; Reitinger T; Linhart W; Muntean W
J Pediatr Orthop; 1999; 19(1):82-3. PubMed ID: 9890293
[TBL] [Abstract][Full Text] [Related]
7. Absence of congenital prethrombotic disorders in children with Legg-Perthes disease.
Sirvent N; Fisher F; el Hayek T; Appert A; Giudicelli H; Griffet J
J Pediatr Orthop B; 2000 Jan; 9(1):24-7. PubMed ID: 10647105
[TBL] [Abstract][Full Text] [Related]
8. Association of antithrombotic factor deficiencies and hypofibrinolysis with Legg-Perthes disease.
Glueck CJ; Crawford A; Roy D; Freiberg R; Glueck H; Stroop D
J Bone Joint Surg Am; 1996 Jan; 78(1):3-13. PubMed ID: 8550676
[TBL] [Abstract][Full Text] [Related]
9. Meta-analysis of hypercoagulability genetic polymorphisms in Perthes disease.
Woratanarat P; Thaveeratitharm C; Woratanarat T; Angsanuntsukh C; Attia J; Thakkinstian A
J Orthop Res; 2014 Jan; 32(1):1-7. PubMed ID: 23983171
[TBL] [Abstract][Full Text] [Related]
10. Does thrombophilia play an aetiological role in Legg-Calvé-Perthes disease?
Hayek S; Kenet G; Lubetsky A; Rosenberg N; Gitel S; Wientroub S
J Bone Joint Surg Br; 1999 Jul; 81(4):686-90. PubMed ID: 10463746
[TBL] [Abstract][Full Text] [Related]
11. Perthes' disease and the search for genetic associations: collagen mutations, Gaucher's disease and thrombophilia.
Kenet G; Ezra E; Wientroub S; Steinberg DM; Rosenberg N; Waldman D; Hayek S
J Bone Joint Surg Br; 2008 Nov; 90(11):1507-11. PubMed ID: 18978274
[TBL] [Abstract][Full Text] [Related]
12. Resistance to activated protein C and Legg-Perthes disease.
Glueck CJ; Brandt G; Gruppo R; Crawford A; Roy D; Tracy T; Stroop D; Wang P; Becker A
Clin Orthop Relat Res; 1997 May; (338):139-52. PubMed ID: 9170375
[TBL] [Abstract][Full Text] [Related]
13. Bilateral Legg-Calve-Perthes Disease and Kienbock's Disease in a Child With Factor V Leiden Thrombophilia: A Case Report.
Baltzer HL; Riester S; Moran SL
Hand (N Y); 2016 Sep; 11(3):NP16-NP19. PubMed ID: 27698645
[No Abstract] [Full Text] [Related]
14. [Congenital disorders of hemostasis in children with Perthes disease].
Kandzierski G; Malek U; Gregosiewicz A; Okoński M; Filiks-Litwin B; Drabko K
Chir Narzadow Ruchu Ortop Pol; 2004; 69(4):225-7. PubMed ID: 15587376
[TBL] [Abstract][Full Text] [Related]
15. The role of coagulation abnormalities in the development of Perthes' disease.
Kealey WD; Mayne EE; McDonald W; Murray P; Cosgrove AP
J Bone Joint Surg Br; 2000 Jul; 82(5):744-6. PubMed ID: 10963178
[TBL] [Abstract][Full Text] [Related]
16. Legg-Perthes disease in three siblings, two heterozygous and one homozygous for the factor V Leiden mutation.
Gruppo R; Glueck CJ; Wall E; Roy D; Wang P
J Pediatr; 1998 May; 132(5):885-8. PubMed ID: 9602208
[TBL] [Abstract][Full Text] [Related]
17. The most severe forms of Perthes' disease associated with the homozygous Factor V Leiden mutation.
Szepesi K; Pósán E; Hársfalvi J; Ajzner E; Szücs G; Gáspár L; Csernátony Z; Udvardy M
J Bone Joint Surg Br; 2004 Apr; 86(3):426-9. PubMed ID: 15125132
[TBL] [Abstract][Full Text] [Related]
18. Protein C and S deficiency, thrombophilia, and hypofibrinolysis: pathophysiologic causes of Legg-Perthes disease.
Glueck CJ; Glueck HI; Greenfield D; Freiberg R; Kahn A; Hamer T; Stroop D; Tracy T
Pediatr Res; 1994 Apr; 35(4 Pt 1):383-8. PubMed ID: 8047373
[TBL] [Abstract][Full Text] [Related]
19. Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease.
Arruda VR; Belangero WD; Ozelo MC; Oliveira GB; Pagnano RG; Volpon JB; Annichino-Bizzacchi JM
J Pediatr Orthop; 1999; 19(1):84-7. PubMed ID: 9890294
[TBL] [Abstract][Full Text] [Related]
20. Association of antithrombotic factor deficiencies and hypofibrinolysis with Legg-Perthes disease.
Kahle WK
J Bone Joint Surg Am; 1997 Jul; 79(7):1114; author reply 1114-5. PubMed ID: 9234890
[No Abstract] [Full Text] [Related]
[Next] [New Search]