Viviane L. Lovatel

Rio De Janeiro, RJ 20230130, Brazil

Last Updated: 09/26/2026

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Found 10 publications

Cytogenetic Abnormalities in Pediatric Myelodysplastic Syndrome: Insights on the Disease Biology and Impact on Leukemic Evolution.

Cytogenetic Abnormalities in Pediatric Myelodysplastic Syndrome: Insights on the Disease Biology and Impact on Leukemic Evolution.

Journal: Biomedicines

Published: September 12, 2025

Identification of Genetic Variants Using Next-Generation Sequencing in Pediatric Myelodysplastic Syndrome: From Disease Biology to Clinical Applications.

Identification of Genetic Variants Using Next-Generation Sequencing in Pediatric Myelodysplastic Syndrome: From Disease Biology to Clinical Applications.

Journal: International journal of molecular sciences

Published: May 08, 2025

Editorial: Pediatric myeloid neoplasms: new insights into diagnosis, prognosis, and treatment.

Editorial: Pediatric myeloid neoplasms: new insights into diagnosis, prognosis, and treatment.

Journal: Frontiers in pediatrics

Published: April 01, 2025

Association between Leukemic Evolution and Uncommon Chromosomal Alterations in Pediatric Myelodysplastic Syndrome.

Association between Leukemic Evolution and Uncommon Chromosomal Alterations in Pediatric Myelodysplastic Syndrome.

Journal: Mediterranean journal of hematology and infectious diseases

Published: September 04, 2023

A Novel Constitutional t(3;8)(p26;q21) and ANKRD26 and SRP72 Variants in a Child with Myelodysplastic Neoplasm: Clinical Implications.

A Novel Constitutional t(3;8)(p26;q21) and ANKRD26 and SRP72 Variants in a Child with Myelodysplastic Neoplasm: Clinical Implications.

Journal: Journal of clinical medicine

Published: March 20, 2023

Global methylation status of LINE-1 in pediatric myelodysplastic syndrome: a predictive biomarker of prognosis?

Global methylation status of LINE-1 in pediatric myelodysplastic syndrome: a predictive biomarker of prognosis?

Journal: Leukemia & lymphoma

Published: September 07, 2022

Acute promyelocytic leukemia in a long-standing HIV-positive patient: Case report and literature review.

Acute promyelocytic leukemia in a long-standing HIV-positive patient: Case report and literature review.

Journal: Leukemia research reports

Published: June 21, 2022

Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well-controlled HIV patient: Case report and literature review.

Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well-controlled HIV patient: Case report and literature review.

Journal: EJHaem

Published: April 23, 2020

An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.

An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia.

Journal: Molecular cytogenetics

Published: May 11, 2018

5meCpG epigenetic marks neighboring a primate-conserved core promoter short tandem repeat indicate X-chromosome inactivation.

5meCpG epigenetic marks neighboring a primate-conserved core promoter short tandem repeat indicate X-chromosome inactivation.

Journal: PloS one

Published: January 22, 2014

Showing 1-10 of 10

Last Updated: 09/26/2026