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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2004 2
2005 1
2007 2
2008 3
2009 9
2010 9
2011 10
2012 5
2013 14
2014 22
2015 11
2016 9
2017 9
2018 3
2019 6
2020 9
2021 7
2022 1
2023 6
2024 11
2025 2

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130 results

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Page 1
Incontinentia pigmenti.
Poziomczyk CS, Recuero JK, Bringhenti L, Maria FD, Campos CW, Travi GM, Freitas AM, Maahs MA, Zen PR, Fiegenbaum M, Almeida ST, Bonamigo RR, Bau AE. Poziomczyk CS, et al. An Bras Dermatol. 2014 Jan-Feb;89(1):26-36. doi: 10.1590/abd1806-4841.20142584. An Bras Dermatol. 2014. PMID: 24626645 Free PMC article. Review.
Blepharophimosis-ptosis-epicanthus inversus syndrome.
Graziadio C, de Moraes FN, Rosa RF, Zen PR, Travi GM, Waldman C, Medina CT, De Baere E, Paskulin GA. Graziadio C, et al. Pediatr Int. 2011 Jun;53(3):390-2. doi: 10.1111/j.1442-200X.2010.03223.x. Pediatr Int. 2011. PMID: 21696507 No abstract available.
Congenital heart defects and extracardiac malformations.
Rosa RC, Rosa RF, Zen PR, Paskulin GA. Rosa RC, et al. Rev Paul Pediatr. 2013 Jun;31(2):243-51. doi: 10.1590/s0103-05822013000200017. Rev Paul Pediatr. 2013. PMID: 23828063 Free article. Review. English, Portuguese.
Nager syndrome and Pierre Robin sequence.
Rosa RF, Guimarães VB, Beltrão LA, Trombetta JS, Lliguin KL, de Mattos VF, Zen PR. Rosa RF, et al. Pediatr Int. 2015 Apr;57(2):e69-72. doi: 10.1111/ped.12562. Epub 2015 Mar 25. Pediatr Int. 2015. PMID: 25808856 Review.
Trisomy 18 and eye anomalies.
Correia JD, da Rosa EB, Silveira DB, Correia EP, Lorenzen MB, Travi GM, Rosa RC, Zen PR, Zen TD, Rosa RF. Correia JD, et al. Am J Med Genet A. 2017 Feb;173(2):553-555. doi: 10.1002/ajmg.a.38036. Epub 2016 Oct 28. Am J Med Genet A. 2017. PMID: 27792864 No abstract available.
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. Among authors: zen prg. 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.
130 results