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Page 1
The mutational spectrum of WT1 in male infertility.
Seabra CM, Quental S, Lima AC, Carvalho F, Gonçalves J, Fernandes S, Pereira I, Silva J, Marques PI, Sousa M, Barros A, Seixas S, Amorim A, Lopes AM. Seabra CM, et al. Among authors: lima ac. J Urol. 2015 May;193(5):1709-15. doi: 10.1016/j.juro.2014.11.004. Epub 2014 Nov 11. J Urol. 2015. PMID: 25451826
Reassessing the Evolutionary History of the 17q21 Inversion Polymorphism.
Alves JM, Lima AC, Pais IA, Amir N, Celestino R, Piras G, Monne M, Comas D, Heutink P, Chikhi L, Amorim A, Lopes AM. Alves JM, et al. Among authors: lima ac. Genome Biol Evol. 2015 Nov 11;7(12):3239-48. doi: 10.1093/gbe/evv214. Genome Biol Evol. 2015. PMID: 26560338 Free PMC article.
Multispecies Purification of Testicular Germ Cells.
Lima AC, Jung M, Rusch J, Usmani A, Lopes A, Conrad DF. Lima AC, et al. Biol Reprod. 2016 Oct 1;95(4):85. doi: 10.1095/biolreprod.116.140566. Epub 2016 Aug 24. Biol Reprod. 2016. PMID: 27557646 Free PMC article.
Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network.
de Oliveira BM, Bernardi FA, Baiochi JF, Neiva MB, Artifon M, Vergara AA, Martins AM, Grumach AS, Acosta AX, Husny ASE, de Freitas Rodrigues Ribeiro B, Ramos CF, Steiner CE, Kim CA, Christofolini DM, Yamada DB, Carvalho EDF, Ribeiro EM, de Arruda Bastos F, Serpa FS, Brandão FR, Adjuto GMAF, Carvalho I, Saute JAM, Junior JCL, Bueno LSM, da Silva LCS, Santos MLSF, Costa MCM, Giusti MMCG, Galera MF, Filho MEC, de Andrade MDFC, De Oliveira Cardoso MT, de Menezes Ferreira MM, Zeny M, Caldato MCF, Sorte NB, Musolino NRC, de Medeiros PFV, Zen PRG, Da Silva RTB, Maia RE, Fock R, Almeida RES, Valle SOR, Amorim T, Teixeira TB, Prazeres VMG, de Faria Ferraz VE, Lima VC, Paiva WJM, Schwartz IVD, Alves D, Félix TM; Raras Network Group. de Oliveira BM, et al. Orphanet J Rare Dis. 2024 Oct 30;19(1):405. doi: 10.1186/s13023-024-03392-7. Orphanet J Rare Dis. 2024. PMID: 39478612 Free PMC article.
Haematopoietic cell transplantation for 106 infants and preschoolers with acquired and inherited bone marrow failures.
Loth G, Dumke CCK, Muratori RR, Pelegrina PD, Peixoto CMA, Bach JLM, Nichele S, Trennepohl JP, Koliski A, Mousquer RTG, Rodrigues AM, Marchesini R, Feitosa MK, Pilonetto DV, Gouvea L, Benini FML, Pirolli ES, Tutumi RAF, Lima ACM, Pasquini R, Bonfim C. Loth G, et al. Among authors: lima acm. Br J Haematol. 2024 Oct 27. doi: 10.1111/bjh.19831. Online ahead of print. Br J Haematol. 2024. PMID: 39462810
356 results