Tavella E - Search Results

1

1p31.1 microdeletion including only NEGR1 gene in two patients.

Tassano E, Uccella S, Giacomini T, Fiorio P, Tavella E, Malacarne M, Gimelli G, Coviello D, Ronchetto P. Tassano E, et al. Among authors: tavella e. Eur J Med Genet. 2020 Jun;63(6):103919. doi: 10.1016/j.ejmg.2020.103919. Epub 2020 Mar 21. Eur J Med Genet. 2020. PMID: 32209393

2

17q23.3 de novo microdeletion involving only TANC2 gene: A new case.

Tassano E, Accogli A, Ronchetto P, Tortora D, Tavella E, Gimelli G, Mancardi M, Malacarne M, Coviello DA. Tassano E, et al. Among authors: tavella e. Eur J Med Genet. 2020 Dec;63(12):104094. doi: 10.1016/j.ejmg.2020.104094. Epub 2020 Nov 4. Eur J Med Genet. 2020. PMID: 33160097

3

Expanding the phenotype associated with interstitial 6p25.1p24.3 microdeletion: a new case and review of the literature.

Tassano E, Uccella S, Severino M, Giacomini T, Nardi F, Gimelli G, Tavella E, Ronchetto P, Malacarne M, Coviello D. Tassano E, et al. Among authors: tavella e. J Genet. 2021;100:9. J Genet. 2021. PMID: 33707360 Free article. Review.

4

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: tavella e. Bone. 2021 Sep;150:116022. doi: 10.1016/j.bone.2021.116022. Epub 2021 May 26. Bone. 2021. PMID: 34048959

5

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: tavella e. Cancer Genet Cytogenet. 2010 Dec;203(2):313-5. doi: 10.1016/j.cancergencyto.2010.08.003. Cancer Genet Cytogenet. 2010. PMID: 21156251

6

Monosomal complex karyotype in pediatric mixed phenotype acute leukemia.

Tassano E, Tavella E, Micalizzi C, Scuderi F, Cuoco C, Morerio C. Tassano E, et al. Among authors: tavella e. Cancer Genet. 2011 Sep;204(9):507-11. doi: 10.1016/j.cancergen.2011.08.015. Cancer Genet. 2011. PMID: 22018273

7

MicroRNA-125b-1 and BLID upregulation resulting from a novel IGH translocation in childhood B-Cell precursor acute lymphoblastic leukemia.

Tassano E, Acquila M, Tavella E, Micalizzi C, Panarello C, Morerio C. Tassano E, et al. Among authors: tavella e. Genes Chromosomes Cancer. 2010 Aug;49(8):682-7. doi: 10.1002/gcc.20776. Genes Chromosomes Cancer. 2010. PMID: 20544842

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: tavella e. Cancer Genet Cytogenet. 2010 Aug;201(1):66-9. doi: 10.1016/j.cancergencyto.2010.05.008. Cancer Genet Cytogenet. 2010. PMID: 20633773

9

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: tavella e. Leuk Lymphoma. 2012 Dec;53(12):2434-8. doi: 10.3109/10428194.2012.695778. Epub 2012 Jun 13. Leuk Lymphoma. 2012. PMID: 22616618

10

Refractory cytopenia of childhood with monosomy 7 presenting as isolated neutropenia in a patient with fragile site at 16q22.

Tassano E, Tavella E, Micalizzi C, Panarello C, Morerio C. Tassano E, et al. Among authors: tavella e. Cancer Genet Cytogenet. 2010 Aug;201(1):70-1. doi: 10.1016/j.cancergencyto.2010.04.020. Cancer Genet Cytogenet. 2010. PMID: 20633774 No abstract available.

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