Barbato IT - Search Results

1

Familial mental retardation: a review and practical classification.

Maris AF, Barbato IT, Trott A, Montano MA. Maris AF, et al. Among authors: barbato it. Cien Saude Colet. 2013 Jun;18(6):1717-29. Cien Saude Colet. 2013. PMID: 23752538 Free article. Review.

2

Long contiguous stretches of homozygosity detected by chromosomal microarrays (CMA) in patients with neurodevelopmental disorders in the South of Brazil.

Chaves TF, Oliveira LF, Ocampos M, Barbato IT, de Luca GR, Barbato Filho JH, de Camargo Pinto LL, Bernardi P, Maris AF. Chaves TF, et al. Among authors: barbato it. 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.

3

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 it. Sci Rep. 2019 Nov 28;9(1):17776. doi: 10.1038/s41598-019-54347-z. Sci Rep. 2019. PMID: 31780800 Free PMC article.

4

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 it. BMC Pediatr. 2020 Nov 4;20(1):506. doi: 10.1186/s12887-020-02382-5. BMC Pediatr. 2020. PMID: 33143672 Free PMC article.

5

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 it. Sci Rep. 2024 Feb 14;14(1):3762. doi: 10.1038/s41598-024-54385-2. Sci Rep. 2024. PMID: 38355898 Free PMC article.

6

Molecular analysis of FMR1 gene in a population in Southern Brazil: Comparison of four methods.

Ramos C, Ocampos M, Barbato IT, Graça Bicalho MD, Nisihara R. Ramos C, et al. Among authors: barbato it. Pract Lab Med. 2020 May 6;21:e00162. doi: 10.1016/j.plabm.2020.e00162. eCollection 2020 Aug. Pract Lab Med. 2020. PMID: 32426440 Free PMC article.

7

Association between mutations in the FMR1 gene and ovarian dysfunction in Brazilian patients.

Ramos C, Ocampos M, Barbato IT, Niehues VMS, Bicalho MDG, Nisihara R. Ramos C, et al. Among authors: barbato it. JBRA Assist Reprod. 2022 Apr 17;26(2):237-240. doi: 10.5935/1518-0557.20210063. JBRA Assist Reprod. 2022. PMID: 34542254 Free PMC article.

8

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.

Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA, Grigsby J, Wegelin JA, Harris S, Lewin F, Weinberg D, Hagerman PJ, Hagerman RJ. Hessl D, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):115-21. doi: 10.1002/ajmg.b.30241. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16184602

9

Autism profiles of males with fragile X syndrome.

Harris SW, Hessl D, Goodlin-Jones B, Ferranti J, Bacalman S, Barbato I, Tassone F, Hagerman PJ, Herman H, Hagerman RJ. Harris SW, et al. Am J Ment Retard. 2008 Nov;113(6):427-38. doi: 10.1352/2008.113:427-438. Am J Ment Retard. 2008. PMID: 19127654 Free PMC article.

10

Quality of life of Brazilian families who have children with Fragile X syndrome: a descriptive study.

Dos Santos TR, Carlucci NSS, de Avó LRDS, Barbato IT, Pinto LLC, Pilotto RF, Germano CMR, Melo DG. Dos Santos TR, et al. Among authors: barbato it. J Community Genet. 2023 Aug;14(4):407-418. doi: 10.1007/s12687-023-00660-0. Epub 2023 Aug 18. J Community Genet. 2023. PMID: 37594660 Free PMC article.

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