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Brazilian Group of Gastrointestinal Tumours' consensus guidelines for the management of oesophageal cancer.
Ecancermedicalscience. 2021 Mar 2;15:1195. doi: 10.3332/ecancer.2021.1195. eCollection 2021.
Ecancermedicalscience. 2021.
PMID: 33889204
Free PMC article.
Brazilian Group of Gastrointestinal Tumours' consensus guidelines for the management of gastric cancer.
Peixoto RD, Rocha-Filho DR, Weschenfelder RF, Rego JFM, Riechelmann R, Coutinho AK, Fernandes GS, Jacome AA, Andrade AC, Murad AM, Mello CAL, Miguel DSCG, Gomes DBD, Racy DJ, Moraes ED, Akaishi EH, Carvalho ES, Mello ES, Filho FM, Coimbra FJF, Capareli FC, Arruda FF, Vieira FMAC, Takeda FR, Cotti GCC, Pereira GLS, Paulo GA, Ribeiro HSC, Lourenco LG, Crosara M, Toneto MG, Oliveira MB, de Lourdes Oliveira M, Begnami MD, Forones NM, Yagi O, Ashton-Prolla P, Aguillar PB, Amaral PCG, Hoff PM, Araujo RLC, Filho RPDP, Gansl RC, Gil RA, Pfiffer TEF, Souza T, Jr UR, Jesus VHF, Jr WLC, Prolla G.
Peixoto RD, et al. Among authors: miguel dscg.
Ecancermedicalscience. 2020 Oct 20;14:1126. doi: 10.3332/ecancer.2020.1126. eCollection 2020.
Ecancermedicalscience. 2020.
PMID: 33209117
Free PMC article.
Review.
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Mucopolysaccharidosis VII in Brazil: natural history and clinical findings.
Giugliani R, Barth AL, Dumas MRC, da Silva Franco JF, de Rosso Giuliani L, Grangeiro CHP, Horovitz DDG, Kim CA, de Araújo Leão EKE, de Medeiros PFV, Miguel DSCG, Moreira MESA, Dos Santos HMGP, da Silva LCS, da Silva LR, de Souza IN, Nalin T, Garcia D.
Giugliani R, et al. Among authors: miguel dscg.
Orphanet J Rare Dis. 2021 May 22;16(1):238. doi: 10.1186/s13023-021-01870-w.
Orphanet J Rare Dis. 2021.
PMID: 34022924
Free PMC article.
Review.
Item in Clipboard
Genotype-phenotype studies in a large cohort of Brazilian patients with Hunter syndrome.
Josahkian JA, Brusius-Facchin AC, Netto ABO, Leistner-Segal S, Málaga DR, Burin MG, Michelin-Tirelli K, Trapp FB, Cardoso-Dos-Santos AC, Ribeiro EM, Kim CA, de Siqueira ACM, Santos ML, do Valle DA, da Silva RTB, Horovitz DDG, de Medeiros PFV, de Souza CFM, Giuliani LR, Miguel DSCG, Santana-da-Silva LC, Galera MF, Giugliani R.
Josahkian JA, et al. Among authors: miguel dscg.
Am J Med Genet C Semin Med Genet. 2021 Sep;187(3):349-356. doi: 10.1002/ajmg.c.31915. Epub 2021 May 7.
Am J Med Genet C Semin Med Genet. 2021.
PMID: 33960103
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Chimerism 47,XY, + 8/46,XX: Follow-up for 11 Years.
de Carvalho AFL, Pitanga PML, Alves ES, Miguel DSCG, Santo LDE, de Araújo AEF, Ornellas ACP, Toralles MBP.
de Carvalho AFL, et al. Among authors: miguel dscg.
J Pediatr Genet. 2020 Dec 7;12(1):81-85. doi: 10.1055/s-0040-1721440. eCollection 2023 Mar.
J Pediatr Genet. 2020.
PMID: 36684553
Free PMC article.
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Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis.
da Silva-Batista JA, Marques W Jr, Oliveira MTJS, Lins LVC, Galvão AJP, Miguel DSCG, Machado-Costa MC.
da Silva-Batista JA, et al. Among authors: miguel dscg.
J Hum Genet. 2020 Aug;65(8):711-713. doi: 10.1038/s10038-020-0749-3. Epub 2020 Apr 9.
J Hum Genet. 2020.
PMID: 32269295
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