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Addition of four doses of rituximab to standard induction chemotherapy in adult patients with precursor B-cell acute lymphoblastic leukaemia (UKALL14): a phase 3, multicentre, randomised controlled trial.
Lancet Haematol. 2022 Apr;9(4):e262-e275. doi: 10.1016/S2352-3026(22)00038-2.
Lancet Haematol. 2022.
PMID: 35358441
Free PMC article.
Clinical Trial.
IKZF1 alterations are not associated with outcome in 498 adults with B-precursor ALL enrolled in the UKALL14 trial.
Mitchell RJ, Kirkwood AA, Barretta E, Clifton-Hadley L, Lawrie E, Lee S, Leongamornlert D, Marks DI, McMillan AK, Menne TF, Papaemmanuil E, Patel B, Patrick P, Rowntree CJ, Zareian N, Alapi KZ, Moorman AV, Fielding AK.
Mitchell RJ, et al. Among authors: alapi kz.
Blood Adv. 2021 Sep 14;5(17):3322-3332. doi: 10.1182/bloodadvances.2021004430.
Blood Adv. 2021.
PMID: 34477813
Free PMC article.
Clinical Trial.
Item in Clipboard
Activation of the LMO2 oncogene through a somatically acquired neomorphic promoter in T-cell acute lymphoblastic leukemia.
Rahman S, Magnussen M, León TE, Farah N, Li Z, Abraham BJ, Alapi KZ, Mitchell RJ, Naughton T, Fielding AK, Pizzey A, Bustraan S, Allen C, Popa T, Pike-Overzet K, Garcia-Perez L, Gale RE, Linch DC, Staal FJT, Young RA, Look AT, Mansour MR.
Rahman S, et al. Among authors: alapi kz.
Blood. 2017 Jun 15;129(24):3221-3226. doi: 10.1182/blood-2016-09-742148. Epub 2017 Mar 7.
Blood. 2017.
PMID: 28270453
Free PMC article.
Item in Clipboard
Prevalence of sequence variants in the RAS-mitogen activated protein kinase signaling pathway in pre-adolescent children with hypertrophic cardiomyopathy.
Kaski JP, Syrris P, Shaw A, Alapi KZ, Cordeddu V, Esteban MT, Jenkins S, Ashworth M, Hammond P, Tartaglia M, McKenna WJ, Elliott PM.
Kaski JP, et al. Among authors: alapi kz.
Circ Cardiovasc Genet. 2012 Jun;5(3):317-26. doi: 10.1161/CIRCGENETICS.111.960468. Epub 2012 May 15.
Circ Cardiovasc Genet. 2012.
PMID: 22589294
Item in Clipboard
Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS gene.
Erdos M, Alapi K, Balogh I, Oroszlán G, Rákóczi E, Sümegi J, Maródi L.
Erdos M, et al.
Exp Hematol. 2006 Nov;34(11):1517-21. doi: 10.1016/j.exphem.2006.06.009.
Exp Hematol. 2006.
PMID: 17046571
Free article.
Item in Clipboard
Recurrent CXCR4 sequence variation in a girl with WHIM syndrome.
Alapi K, Erdos M, Kovács G, Maródi L.
Alapi K, et al.
Eur J Haematol. 2007 Jan;78(1):86-8. doi: 10.1111/j.1600-0609.2006.00779.x. Epub 2006 Nov 6.
Eur J Haematol. 2007.
PMID: 17087743
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Retrospective diagnosis of X-linked hyper-IgM syndrome in a family with multiple deaths of affected males.
Erdos M, Alapi K, Maródi L.
Erdos M, et al.
Haematologica. 2007 Feb;92(2):281-2. doi: 10.3324/haematol.10172.
Haematologica. 2007.
PMID: 17296592
Free article.
Item in Clipboard
Prenatal diagnosis of the WAS R86H sequence variation in heterozygous twins.
Alapi K, Erdos M, Török O, Maródi L.
Alapi K, et al.
Clin Chem. 2006 May;52(5):901-3. doi: 10.1373/clinchem.2005.064816.
Clin Chem. 2006.
PMID: 16638962
No abstract available.
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