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2012 1
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2020 1
2022 1
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Page 1
Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease.
Delea M, Massara LS, Espeche LD, Bidondo MP, Barbero P, Oliveri J, Brun P, Fabro M, Galain M, Fernández CS, Taboas M, Bruque CD, Kolomenski JE, Izquierdo A, Berenstein A, Cosentino V, Martinoli C, Vilas M, Rittler M, Mendez R, Furforo L, Liascovich R, Groisman B, Rozental S, Dain L, On Behalf Of The Pid Acm-Cc Group. Delea M, et al. Among authors: oliveri j. Genes (Basel). 2022 Jun 29;13(7):1172. doi: 10.3390/genes13071172. Genes (Basel). 2022. PMID: 35885957 Free PMC article.
Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Delea M, Espeche LD, Bruque CD, Bidondo MP, Massara LS, Oliveri J, Brun P, Cosentino VR, Martinoli C, Tolaba N, Picon C, Ponce Zaldua ME, Ávila S, Gutnisky V, Perez M, Furforo L, Buzzalino ND, Liascovich R, Groisman B, Rittler M, Rozental S, Barbero P, Dain L. Delea M, et al. Among authors: oliveri j. Genes (Basel). 2018 Sep 11;9(9):454. doi: 10.3390/genes9090454. Genes (Basel). 2018. PMID: 30208644 Free PMC article.
Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings.
Calandra CR, Mocarbel Y, Vishnopolska SA, Toneguzzo V, Oliveri J, Cazado EC, Biagioli G, Turjanksi AG, Marti M. Calandra CR, et al. Among authors: oliveri j. Mov Disord Clin Pract. 2019 Jan 16;6(3):259-262. doi: 10.1002/mdc3.12721. eCollection 2019 Mar. Mov Disord Clin Pract. 2019. PMID: 30949559 Free PMC article. No abstract available.
Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation.
Calandra CR, Buda G, Vishnopolska SA, Oliveri J, Olivieri FA, Pérez Millán MI, Biagioli G, Miquelini LA, Pellene AL, Marti MA. Calandra CR, et al. Among authors: oliveri j. Parkinsonism Relat Disord. 2020 Apr;73:52-54. doi: 10.1016/j.parkreldis.2020.03.020. Epub 2020 Mar 24. Parkinsonism Relat Disord. 2020. PMID: 32248051 No abstract available.