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Long contiguous stretches of homozygosity detected by chromosomal microarrays (CMA) in patients with neurodevelopmental disorders in the South of Brazil.
BMC Med Genomics. 2019 Mar 12;12(1):50. doi: 10.1186/s12920-019-0496-5.
BMC Med Genomics. 2019.
PMID: 30866944
Free PMC article.
Epstein-Barr virus acute encephalomyelitis in a 13-year-old boy.
Grillo E, da Silva RJ, Barbato Filho JH.
Grillo E, et al. Among authors: barbato filho jh.
Eur J Paediatr Neurol. 2008 Sep;12(5):417-20. doi: 10.1016/j.ejpn.2007.10.016. Epub 2007 Dec 3.
Eur J Paediatr Neurol. 2008.
PMID: 18054506
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A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD.
Chaves TF, Ocampos M, Barbato IT, de Camargo Pinto LL, de Luca GR, Barbato Filho JH, Bernardi P, Costa Netto Muniz Y, Francesca Maris A.
Chaves TF, et al. Among authors: barbato filho jh.
Sci Rep. 2024 Feb 14;14(1):3762. doi: 10.1038/s41598-024-54385-2.
Sci Rep. 2024.
PMID: 38355898
Free PMC article.
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Etiology of intellectual disability in individuals from special education schools in the south of Brazil.
Oliveira LF, Chaves TF, Baretto N, de Luca GR, Barbato IT, Barbato Filho JH, Ocampos M, Maris AF.
Oliveira LF, et al. Among authors: barbato filho jh.
BMC Pediatr. 2020 Nov 4;20(1):506. doi: 10.1186/s12887-020-02382-5.
BMC Pediatr. 2020.
PMID: 33143672
Free PMC article.
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Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders From the South of Brazil.
Chaves TF, Baretto N, Oliveira LF, Ocampos M, Barbato IT, Anselmi M, De Luca GR, Barbato Filho JH, Pinto LLC, Bernardi P, Maris AF.
Chaves TF, et al. Among authors: barbato filho jh.
Sci Rep. 2019 Nov 28;9(1):17776. doi: 10.1038/s41598-019-54347-z.
Sci Rep. 2019.
PMID: 31780800
Free PMC article.
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