Abdelhaleem M - Search Results

1

Malignant hematological disorders in children with Wolf-Hirschhorn syndrome.

Sharathkumar A, Kirby M, Freedman M, Abdelhaleem M, Chitayat D, Teshima IE, Dror Y. Sharathkumar A, et al. Among authors: abdelhaleem m. Am J Med Genet A. 2003 Jun 1;119A(2):194-9. doi: 10.1002/ajmg.a.20080. Am J Med Genet A. 2003. PMID: 12749063

2

Isochromosome (17)(q10) and translocation (4;12)(q12;p13) in a child with acute myeloid leukemia.

Nathan PC, Chun K, Abdelhaleem M, Malkin D. Nathan PC, et al. Among authors: abdelhaleem m. Cancer Genet Cytogenet. 2001 Nov;131(1):82-5. doi: 10.1016/s0165-4608(01)00494-0. Cancer Genet Cytogenet. 2001. PMID: 11734325

3

Thrombocytopenia and megakaryocyte dysplasia: an adverse effect of valproic acid treatment.

Gesundheit B, Kirby M, Lau W, Koren G, Abdelhaleem M. Gesundheit B, et al. Among authors: abdelhaleem m. J Pediatr Hematol Oncol. 2002 Oct;24(7):589-90. doi: 10.1097/00043426-200210000-00022. J Pediatr Hematol Oncol. 2002. PMID: 12368704 No abstract available.

4

The evolution of juvenile myelomonocytic leukemia in a female patient with paternally inherited neurofibromatosis type 1.

Leung EW, Vanek W, Abdelhaleem M, Freedman MH, Dror Y. Leung EW, et al. Among authors: abdelhaleem m. J Pediatr Hematol Oncol. 2003 Feb;25(2):145-7. doi: 10.1097/00043426-200302000-00012. J Pediatr Hematol Oncol. 2003. PMID: 12571467

5

Transient myelodysplastic syndrome associated with isochromosome 7q abnormality.

Leung EW, Woodman RC, Roland B, Abdelhaleem M, Freedman MH, Dror Y. Leung EW, et al. Among authors: abdelhaleem m. Pediatr Hematol Oncol. 2003 Oct-Nov;20(7):539-45. doi: 10.1080/08880010390232754. Pediatr Hematol Oncol. 2003. PMID: 12959859

6

A der(19)t(12;19)(q12;p13.3) in a case of pediatric acute leukemia with unusual immunophenotype.

Leung E, Teshima I, Ye C, Grant R, Abdelhaleem M. Leung E, et al. Among authors: abdelhaleem m. Cancer Genet Cytogenet. 2005 Mar;157(2):164-8. doi: 10.1016/j.cancergencyto.2004.08.027. Cancer Genet Cytogenet. 2005. PMID: 15721640

7

Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet alpha-granule biogenesis.

Lo B, Li L, Gissen P, Christensen H, McKiernan PJ, Ye C, Abdelhaleem M, Hayes JA, Williams MD, Chitayat D, Kahr WH. Lo B, et al. Among authors: abdelhaleem m. Blood. 2005 Dec 15;106(13):4159-66. doi: 10.1182/blood-2005-04-1356. Epub 2005 Aug 25. Blood. 2005. PMID: 16123220 Free article.

8

Shwachman-Diamond syndrome: an inherited model of aplastic anaemia with accelerated angiogenesis.

Leung EW, Rujkijyanont P, Beyene J, Wei K, Abdelhaleem M, Freedman MH, Dror Y. Leung EW, et al. Among authors: abdelhaleem m. Br J Haematol. 2006 Jun;133(5):558-61. doi: 10.1111/j.1365-2141.2006.06069.x. Br J Haematol. 2006. PMID: 16681645

9

Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia.

Shah N, Leaker MT, Teshima I, Baruchel S, Abdelhaleem M, Ye CC. Shah N, et al. Among authors: abdelhaleem m. Pediatr Blood Cancer. 2008 May;50(5):1052-3. doi: 10.1002/pbc.21317. Pediatr Blood Cancer. 2008. PMID: 18213712

10

Response to treatment with azacitidine in children with advanced myelodysplastic syndrome prior to hematopoietic stem cell transplantation.

Waespe N, Van Den Akker M, Klaassen RJ, Lieberman L, Irwin MS, Ali SS, Abdelhaleem M, Zlateska B, Liebman M, Cada M, Schechter T, Dror Y. Waespe N, et al. Among authors: abdelhaleem m. Haematologica. 2016 Dec;101(12):1508-1515. doi: 10.3324/haematol.2016.145821. Epub 2016 Aug 18. Haematologica. 2016. PMID: 27540140 Free PMC article.

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