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Year Number of Results
1993 1
1999 1
2006 2
2007 1
2008 2
2009 4
2010 1
2011 3
2012 3
2013 5
2014 5
2015 2
2016 1
2018 1
2019 2
2020 3
2021 3
2022 2
2025 0

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35 results

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Page 1
Autism and Down syndrome: early identification and diagnosis.
Diniz NLF, Parlato-Oliveira E, Pimenta PGA, Araújo LA, Valadares ER. Diniz NLF, et al. Among authors: valadares er. Arq Neuropsiquiatr. 2022 Jun;80(6):620-630. doi: 10.1590/0004-282X-ANP-2021-0156. Arq Neuropsiquiatr. 2022. PMID: 35946706 Free PMC article.
Guidelines for the management of mucopolysaccharidosis type I.
Martins AM, Dualibi AP, Norato D, Takata ET, Santos ES, Valadares ER, Porta G, de Luca G, Moreira G, Pimentel H, Coelho J, Brum JM, Semionato Filho J, Kerstenetzky MS, Guimarães MR, Rojas MV, Aranda PC, Pires RF, Faria RG, Mota RM, Matte U, Guedes ZC. Martins AM, et al. Among authors: valadares er. J Pediatr. 2009 Oct;155(4 Suppl):S32-46. doi: 10.1016/j.jpeds.2009.07.005. J Pediatr. 2009. PMID: 19765409 Review. No abstract available.
Oral health of Brazilian individuals with mucopolyssaccaridosis.
Deps TD, França EC, Valadares ER, Nicolau B, Pordeus IA, Borges-Oliveira AC. Deps TD, et al. Among authors: valadares er. Eur Arch Paediatr Dent. 2021 Feb;22(1):13-19. doi: 10.1007/s40368-020-00508-y. Epub 2020 Jan 31. Eur Arch Paediatr Dent. 2021. PMID: 32006273
Recommendations on diagnosis, treatment, and monitoring for Gaucher disease.
Martins AM, Valadares ER, Porta G, Coelho J, Semionato Filho J, Pianovski MA, Kerstenetzky MS, Montoril Mde F, Aranda PC, Pires RF, Mota RM, Bortolheiro TC; Brazilian Study Group on Gaucher Disease and other Lysosomal Storage Diseases. Martins AM, et al. Among authors: valadares er. J Pediatr. 2009 Oct;155(4 Suppl):S10-8. doi: 10.1016/j.jpeds.2009.07.004. J Pediatr. 2009. PMID: 19765407 Review. No abstract available.
Neuropsychiatric and sleep study in autosomal dominant dopa-responsive dystonia.
Alves Júnior AC, Daker MV, Machado AMC, Luna AS, Valladares Neto DC, Valadares ER. Alves Júnior AC, et al. Among authors: valadares er. Mol Genet Metab Rep. 2022 Apr 18;31:100870. doi: 10.1016/j.ymgmr.2022.100870. eCollection 2022 Jun. Mol Genet Metab Rep. 2022. PMID: 35782624 Free PMC article.
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.
Moosa S, Yamamoto GL, Garbes L, Keupp K, Beleza-Meireles A, Moreno CA, Valadares ER, de Sousa SB, Maia S, Saraiva J, Honjo RS, Kim CA, Cabral de Menezes H, Lausch E, Lorini PV, Lamounier A Jr, Carniero TCB, Giunta C, Rohrbach M, Janner M, Semler O, Beleggia F, Li Y, Yigit G, Reintjes N, Altmüller J, Nürnberg P, Cavalcanti DP, Zabel B, Warman ML, Bertola DR, Wollnik B, Netzer C. Moosa S, et al. Among authors: valadares er. Am J Hum Genet. 2019 Oct 3;105(4):836-843. doi: 10.1016/j.ajhg.2019.08.008. Epub 2019 Sep 26. Am J Hum Genet. 2019. PMID: 31564437 Free PMC article.
Neurofibromatoses: part 1 - diagnosis and differential diagnosis.
Rodrigues LO, Batista PB, Goloni-Bertollo EM, de Souza-Costa D, Eliam L, Eliam M, Cunha KS, Darrigo-Junior LG, Ferraz-Filho JR, Geller M, Gianordoli-Nascimento IF, Madeira LG, Malloy-Diniz LF, Mendes HM, de Miranda DM, Pavarino EC, Baptista-Pereira L, Rezende NA, Rodrigues Lde O, da Silva CM, de Souza JF, de Souza ML, Stangherlin A, Valadares ER, Vidigal PV. Rodrigues LO, et al. Among authors: valadares er. Arq Neuropsiquiatr. 2014 Mar;72(3):241-50. doi: 10.1590/0004-282x20130241. Arq Neuropsiquiatr. 2014. PMID: 24676443 Free article.
De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females.
Li D, Strong A, Shen KM, Cassiman D, Van Dyck M, Linhares ND, Valadares ER, Wang T, Pena SDJ, Jaeken J, Vergano S, Zackai E, Hing A, Chow P, Ganguly A, Scholz T, Bierhals T, Philipp D, Hakonarson H, Bhoj E. Li D, et al. Among authors: valadares er. Genet Med. 2021 Apr;23(4):637-644. doi: 10.1038/s41436-020-01031-7. Epub 2020 Nov 27. Genet Med. 2021. PMID: 33244166 Free article.
Clinical Characterization of Mucolipidoses II and III: A Multicenter Study.
Alegra T, Sperb-Ludwig F, Guarany NR, Ribeiro EM, Lourenço CM, Kim CA, Valadares ER, Galera MF, Acosta AX, Horovitz DDG, Schwartz IVD. Alegra T, et al. Among authors: valadares er. J Pediatr Genet. 2019 Dec;8(4):198-204. doi: 10.1055/s-0039-1697605. Epub 2019 Sep 24. J Pediatr Genet. 2019. PMID: 31687257 Free PMC article.
35 results