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1,435 results

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Page 1
Outcome of pediatric thromboembolic disease: a report from the Canadian Childhood Thrombophilia Registry.
Monagle P, Adams M, Mahoney M, Ali K, Barnard D, Bernstein M, Brisson L, David M, Desai S, Scully MF, Halton J, Israels S, Jardine L, Leaker M, McCusker P, Silva M, Wu J, Anderson R, Andrew M, Massicotte MP. Monagle P, et al. Among authors: ali k. Pediatr Res. 2000 Jun;47(6):763-6. doi: 10.1203/00006450-200006000-00013. Pediatr Res. 2000. PMID: 10832734
Chronic immune thrombocytopenic purpura in children: a survey of the canadian experience.
Belletrutti M, Ali K, Barnard D, Blanchette V, Chan A, David M, Luke B, Price V, Ritchie B, Wu J; Canadian Pediatric Chronic ITP Working Group; Canadian Pediatric Thrombosis and Hemostasis Network. Belletrutti M, et al. Among authors: ali k. J Pediatr Hematol Oncol. 2007 Feb;29(2):95-100. doi: 10.1097/MPH.0b013e3180320b36. J Pediatr Hematol Oncol. 2007. PMID: 17279005
Disease progression in recently diagnosed patients with inherited marrow failure syndromes: a Canadian Inherited Marrow Failure Registry (CIMFR) report.
Steele JM, Sung L, Klaassen R, Fernandez CV, Yanofsky R, Wu J, Odame I, Silva M, Champagne J, Ali K, Brossard J, Samson Y, Abish S, Le D, Jardine L, Hand JP, Lipton JH, Charpentier K, Stephens D, Freedman M, Dror Y; Canadian Inherited Marrow Failure Registry. Steele JM, et al. Among authors: ali k. Pediatr Blood Cancer. 2006 Dec;47(7):918-25. doi: 10.1002/pbc.20876. Pediatr Blood Cancer. 2006. PMID: 16676307
A survey of factor prophylaxis in the Canadian haemophilia A population.
Blanchette P, Rivard G, Israels S, Robinson S, Ali K, Walker I, Stain AM, Blanchette V; Association of Hemophilia Clinic Directors of Canada and Canadian Association of Nurses in Hemophilia Care. Blanchette P, et al. Among authors: ali k. Haemophilia. 2004 Nov;10(6):679-83. doi: 10.1111/j.1365-2516.2004.01045.x. Haemophilia. 2004. PMID: 15569161
Genetic analysis of inherited bone marrow failure syndromes from one prospective, comprehensive and population-based cohort and identification of novel mutations.
Tsangaris E, Klaassen R, Fernandez CV, Yanofsky R, Shereck E, Champagne J, Silva M, Lipton JH, Brossard J, Michon B, Abish S, Steele M, Ali K, Dower N, Athale U, Jardine L, Hand JP, Odame I, Canning P, Allen C, Carcao M, Beyene J, Roifman CM, Dror Y. Tsangaris E, et al. Among authors: ali k. J Med Genet. 2011 Sep;48(9):618-28. doi: 10.1136/jmg.2011.089821. Epub 2011 Jun 9. J Med Genet. 2011. PMID: 21659346
Comparative analysis of Shwachman-Diamond syndrome to other inherited bone marrow failure syndromes and genotype-phenotype correlation.
Hashmi SK, Allen C, Klaassen R, Fernandez CV, Yanofsky R, Shereck E, Champagne J, Silva M, Lipton JH, Brossard J, Samson Y, Abish S, Steele M, Ali K, Dower N, Athale U, Jardine L, Hand JP, Beyene J, Dror Y. Hashmi SK, et al. Among authors: ali k. Clin Genet. 2011 May;79(5):448-58. doi: 10.1111/j.1399-0004.2010.01468.x. Clin Genet. 2011. PMID: 20569259
1,435 results