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Global methylation status of LINE-1 in pediatric myelodysplastic syndrome: a predictive biomarker of prognosis?
Leuk Lymphoma. 2022 Dec;63(14):3484-3487. doi: 10.1080/10428194.2022.2115842. Epub 2022 Sep 7.
Leuk Lymphoma. 2022.
PMID: 36070601
No abstract available.
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.
Lovatel VL, de Souza DC, Alvarenga TF, Capela de Matos RR, Diniz C, Schramm MT, Llerena Júnior JC, Silva MLM, Abdelhay E, de Souza Fernandez T.
Lovatel VL, et al.
Mol Cytogenet. 2018 Jul 11;11:40. doi: 10.1186/s13039-018-0389-x. eCollection 2018.
Mol Cytogenet. 2018.
PMID: 30008805
Free PMC article.
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A Novel Constitutional t(3;8)(p26;q21) and ANKRD26 and SRP72 Variants in a Child with Myelodysplastic Neoplasm: Clinical Implications.
Lovatel VL, Bueno AP, Kós EAA, Meyer LGC, Ferreira GM, Kalonji MF, Mello FV, Milito CB, Costa ESD, Abdelhay E, Redondo MDT, Pombo-de-Oliveira MS, Fernandez TS.
Lovatel VL, et al.
J Clin Med. 2023 Apr 28;12(9):3171. doi: 10.3390/jcm12093171.
J Clin Med. 2023.
PMID: 37176611
Free PMC article.
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Acute promyelocytic leukemia in a long-standing HIV-positive patient: Case report and literature review.
Mendes-de-Almeida DP, Fernandez TS, Lovatel VL, da Rocha MM, Gomes BE, Monte-Mór BCR, Vianna DT, Alcoforado MTG, Kronemberg JMPB, Cardoso JPSC, Oliveira VDG, Bokel J, Vizzoni AG, Nunes EP, Grinsztejn B.
Mendes-de-Almeida DP, et al. Among authors: lovatel vl.
Leuk Res Rep. 2022 Jul 26;18:100339. doi: 10.1016/j.lrr.2022.100339. eCollection 2022.
Leuk Res Rep. 2022.
PMID: 35958242
Free PMC article.
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Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well-controlled HIV patient: Case report and literature review.
Mendes-de-Almeida DP, Lovatel VL, Dos Santos-Bueno FV, de Kós EAA, Andrade FG, Schramm MT, Nunes EP, Grinsztejn BGJ, Pombo-de-Oliveira MS, Fernandez TS.
Mendes-de-Almeida DP, et al. Among authors: lovatel vl.
EJHaem. 2020 Jun 2;1(1):344-349. doi: 10.1002/jha2.14. eCollection 2020 Jul.
EJHaem. 2020.
PMID: 35847703
Free PMC article.
No abstract available.
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Association between Leukemic Evolution and Uncommon Chromosomal Alterations in Pediatric Myelodysplastic Syndrome.
Lovatel VL, da Silva BF, Rodrigues EF, da Rosa Borges MLR, de Cássia Barbosa Tavares R, Bueno APS, da Costa ES, de Jesus Marques Salles T, de Souza Fernandez T.
Lovatel VL, et al.
Mediterr J Hematol Infect Dis. 2024 Jan 1;16(1):e2024003. doi: 10.4084/MJHID.2024.003. eCollection 2024.
Mediterr J Hematol Infect Dis. 2024.
PMID: 38223485
Free PMC article.
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5meCpG epigenetic marks neighboring a primate-conserved core promoter short tandem repeat indicate X-chromosome inactivation.
Machado FB, Machado FB, Faria MA, Lovatel VL, Alves da Silva AF, Radic CP, De Brasi CD, Rios ÁF, de Sousa Lopes SM, da Silveira LS, Ruiz-Miranda CR, Ramos ES, Medina-Acosta E.
Machado FB, et al. Among authors: lovatel vl.
PLoS One. 2014 Jul 31;9(7):e103714. doi: 10.1371/journal.pone.0103714. eCollection 2014.
PLoS One. 2014.
PMID: 25078280
Free PMC article.
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