Maurer-Morelli CV - Search Results

1

Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia.

Simioni M, Vieira TP, Sgardioli IC, Freitas EL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Gil-da-Silva-Lopes VL. Simioni M, et al. Am J Med Genet A. 2012 Nov;158A(11):2905-10. doi: 10.1002/ajmg.a.35603. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991255

2

Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate.

Araújo TK, Simioni M, Félix TM, de Souza LT, Fontes MÍ, Monlleó IL, Souza J, Fett-Conte AC, Secolin R, Lopes-Cendes I, Maurer-Morelli CV, Gil-da-Silva-Lopes VL. Araújo TK, et al. Plast Surg Int. 2012;2012:247104. doi: 10.1155/2012/247104. Epub 2012 Nov 27. Plast Surg Int. 2012. PMID: 23227324 Free PMC article.

3

Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation.

Simioni M, Araujo TK, Monlleo IL, Maurer-Morelli CV, Gil-da-Silva-Lopes VL. Simioni M, et al. J Hum Genet. 2015 Jan;60(1):17-25. doi: 10.1038/jhg.2014.96. Epub 2014 Nov 13. J Hum Genet. 2015. PMID: 25391604

4

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy.

Secolin R, Maurer-Morelli C, Cendes F, Lopes-Cendes I. Secolin R, et al. Epilepsia. 2010 Feb;51 Suppl 1:47-50. doi: 10.1111/j.1528-1167.2009.02445.x. Epilepsia. 2010. PMID: 20331715 Free article. No abstract available.

5

Indomethacin treatment prior to pentylenetetrazole-induced seizures downregulates the expression of il1b and cox2 and decreases seizure-like behavior in zebrafish larvae.

Barbalho PG, Lopes-Cendes I, Maurer-Morelli CV. Barbalho PG, et al. BMC Neurosci. 2016 Mar 9;17:12. doi: 10.1186/s12868-016-0246-y. BMC Neurosci. 2016. PMID: 26961169 Free PMC article.

6

Cyclooxygenase-1 as a Potential Therapeutic Target for Seizure Suppression: Evidences from Zebrafish Pentylenetetrazole-Seizure Model.

Barbalho PG, Carvalho BS, Lopes-Cendes I, Maurer-Morelli CV. Barbalho PG, et al. Among authors: maurer morelli cv. Front Neurol. 2016 Nov 15;7:200. doi: 10.3389/fneur.2016.00200. eCollection 2016. Front Neurol. 2016. PMID: 27895618 Free PMC article.

7

Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.

França MC Jr, D'Abreu A, Maurer-Morelli CV, Seccolin R, Appenzeller S, Alessio A, Damasceno BP, Nucci A, Cendes F, Lopes-Cendes I. França MC Jr, et al. Mov Disord. 2007 Aug 15;22(11):1556-62. doi: 10.1002/mds.21480. Mov Disord. 2007. PMID: 17516453

8

LINKGEN: a new algorithm to process data in genetic linkage studies.

Secolin R, Rocha CS, Torres FR, Santos ML, Maurer-Morelli CV, Santos NF, Lopes-Cendes I. Secolin R, et al. Genomics. 2008 Jun;91(6):544-7. doi: 10.1016/j.ygeno.2008.02.001. Epub 2008 Apr 2. Genomics. 2008. PMID: 18378114 Free article.

9

A Locus Identified on Chromosome18P11.31 is Associated with Hippocampal Abnormalities in a Family with Mesial Temporal Lobe Epilepsy.

Maurer-Morelli CV, Secolin R, Morita ME, Domingues RR, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. Maurer-Morelli CV, et al. Front Neurol. 2012 Aug 10;3:124. doi: 10.3389/fneur.2012.00124. eCollection 2012. Front Neurol. 2012. PMID: 23015801 Free PMC article.

10

THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy.

Maurer-Morelli CV, Secolin R, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I. Maurer-Morelli CV, et al. Epilepsy Res. 2006 Oct;71(2-3):233-6. doi: 10.1016/j.eplepsyres.2006.06.016. Epub 2006 Aug 17. Epilepsy Res. 2006. PMID: 16914293

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