Morerio C - Search Results

1

Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness.

Tassano E, Uccella S, Ronchetto P, Martinheira Da Silva JS, Viaggi S, Mancardi M, Ramenghi L, Murri A, Biondi M, Gimelli G, Morerio C, Malacarne M, Coviello D. Tassano E, et al. Among authors: morerio c. Cytogenet Genome Res. 2022;162(3):132-139. doi: 10.1159/000525181. Epub 2022 Jul 27. Cytogenet Genome Res. 2022. PMID: 35896065

2

Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption.

Tassano E, Ronchetto P, Severino M, Divizia MT, Lerone M, Uccella S, Nobili L, Tavella E, Morerio C, Coviello D, Malacarne M. Tassano E, et al. Among authors: morerio c. Bone. 2021 Sep;150:116022. doi: 10.1016/j.bone.2021.116022. Epub 2021 May 26. Bone. 2021. PMID: 34048959

3

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Tassano E, Sementa AR, Tavella E, Garaventa A, Panarello C, Morerio C. Tassano E, et al. Among authors: morerio c. Cancer Genet Cytogenet. 2010 Dec;203(2):313-5. doi: 10.1016/j.cancergencyto.2010.08.003. Cancer Genet Cytogenet. 2010. PMID: 21156251

4

MLL-MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia.

Morerio C, Rapella A, Tassano E, Rosanda C, Panarello C. Morerio C, et al. Leuk Res. 2005 Oct;29(10):1223-6. doi: 10.1016/j.leukres.2005.03.008. Epub 2005 Apr 11. Leuk Res. 2005. PMID: 16111539 Review.

5

Differential diagnosis of lipoma-like lipoblastoma.

Morerio C, Nozza P, Tassano E, Rosanda C, Granata C, Conte M, Panarello C. Morerio C, et al. Pediatr Blood Cancer. 2009 Jan;52(1):132-4. doi: 10.1002/pbc.21747. Pediatr Blood Cancer. 2009. PMID: 18798558

6

New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6.

Tassano E, Tavella E, Valli R, Micalizzi C, Cuoco C, Maserati E, Pasquali F, Morerio C. Tassano E, et al. Among authors: morerio c. Leuk Lymphoma. 2012 Dec;53(12):2434-8. doi: 10.3109/10428194.2012.695778. Epub 2012 Jun 13. Leuk Lymphoma. 2012. PMID: 22616618

7

Inversion (11)(p15q22) with NUP98-DDX10 fusion gene in pediatric acute myeloid leukemia.

Morerio C, Acquila M, Rapella A, Tassano E, Rosanda C, Panarello C. Morerio C, et al. Cancer Genet Cytogenet. 2006 Dec;171(2):122-5. doi: 10.1016/j.cancergencyto.2006.07.002. Cancer Genet Cytogenet. 2006. PMID: 17116492 Review.

8

Cytogenetic characterization of a fibrous hamartoma of infancy with complex translocations.

Tassano E, Nozza P, Tavella E, Garaventa A, Panarello C, Morerio C. Tassano E, et al. Among authors: morerio c. Cancer Genet Cytogenet. 2010 Aug;201(1):66-9. doi: 10.1016/j.cancergencyto.2010.05.008. Cancer Genet Cytogenet. 2010. PMID: 20633773

9

Gain of 1q in pediatric myelodysplastic syndromes.

Morerio C, Rapella A, Tassano E, Lanino E, Micalizzi C, Rosanda C, Panarello C. Morerio C, et al. Leuk Res. 2006 Nov;30(11):1437-41. doi: 10.1016/j.leukres.2005.12.022. Epub 2006 Feb 10. Leuk Res. 2006. PMID: 16472857

10

t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia.

Morerio C, Acquila M, Rosanda C, Rapella A, Tassano E, Micalizzi C, Panarello C. Morerio C, et al. Leuk Res. 2005 Apr;29(4):467-70. doi: 10.1016/j.leukres.2004.09.002. Epub 2004 Dec 9. Leuk Res. 2005. PMID: 15725483

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