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Year Number of Results
1980 1
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100 results

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Page 1
Pediatric Hodgkin Lymphoma, Version 3.2021.
Flerlage JE, Hiniker SM, Armenian S, Benya EC, Bobbey AJ, Chang V, Cooper S, Coulter DW, Cuglievan B, Hoppe BS, Isenalumhe L, Kelly K, Kersun L, Lamble AJ, Larrier NA, Magee J, Oduro K, Pacheco M, Price AP, Roberts KB, Smith CM, Sohani AR, Trovillion EM, Walling E, Xavier AC, Burns JL, Campbell M. Flerlage JE, et al. Among authors: xavier ac. J Natl Compr Canc Netw. 2021 Jun 30;19(6):733-754. doi: 10.6004/jnccn.2021.0027. J Natl Compr Canc Netw. 2021. PMID: 34214968
Genomic imbalances in craniofacial microsomia.
Spineli-Silva S, Sgardioli IC, Dos Santos AP, Bergamini LL, Monlleó IL, Fontes MIB, Félix TM, Ribeiro EM, Xavier AC, Lustosa-Mendes E, Gil-da-Silva-Lopes VL, Vieira TP. Spineli-Silva S, et al. Among authors: xavier ac. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):970-985. doi: 10.1002/ajmg.c.31857. Epub 2020 Nov 20. Am J Med Genet C Semin Med Genet. 2020. PMID: 33215817 Review.
Evaluation of prognostic factors in patients with high-risk classical Hodgkin lymphoma undergoing autologous transplantation.
Epperla N, Huang Y, Cashen AF, Vaughn JL, Hanel W, Badar T, Barta SK, Caimi PF, Sethi TK, Reddy N, Karmali R, Bello C, Chavez JC, Kothari SK, Hernandez-Ilizaliturri FJ, Svoboda J, Lansigan F, Glenn MJ, Cohen JB, Sorge C, Christian B, Herrera AF, Hamadani M, Costa LJ, Xavier AC. Epperla N, et al. Among authors: xavier ac. Blood Adv. 2024 Nov 12;8(21):5458-5466. doi: 10.1182/bloodadvances.2024013743. Blood Adv. 2024. PMID: 39213424 Free PMC article.
COVID-19 and childhood acute lymphoblastic leukemia.
Taub JW, Ge Y, Xavier AC. Taub JW, et al. Among authors: xavier ac. Pediatr Blood Cancer. 2020 Jul;67(7):e28400. doi: 10.1002/pbc.28400. Epub 2020 May 13. Pediatr Blood Cancer. 2020. PMID: 32400927 Free PMC article. No abstract available.
Acute leukemia in children with Down syndrome.
Xavier AC, Taub JW. Xavier AC, et al. Haematologica. 2010 Jul;95(7):1043-5. doi: 10.3324/haematol.2010.024968. Haematologica. 2010. PMID: 20595099 Free PMC article. Review. No abstract available.
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.
de Wallau MB, Xavier AC, Moreno CA, Kim CA, Mendes EL, Ribeiro EM, Oliveira A, Félix TM, Fett-Conte AC, Bonadia LC, Correia-Costa GR, Monlleó IL, Gil-da-Silva-Lopes VL, Vieira TP. de Wallau MB, et al. Among authors: xavier ac. Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518. Genes (Basel). 2024. PMID: 38674452 Free PMC article.
100 results