Grazina M - Search Results

1

Antenatal manifestations of mitochondrial disorders.

Tavares MV, Santos MJ, Domingues AP, Pratas J, Mendes C, Simões M, Moura P, Diogo L, Grazina M. Tavares MV, et al. Among authors: grazina m. J Inherit Metab Dis. 2013 Sep;36(5):805-11. doi: 10.1007/s10545-012-9567-x. Epub 2013 Jan 30. J Inherit Metab Dis. 2013. PMID: 23361304

2

Frontotemporal dementia and mitochondrial DNA transitions.

Grazina M, Silva F, Santana I, Santiago B, Mendes C, Simões M, Oliveira M, Cunha L, Oliveira C. Grazina M, et al. Neurobiol Dis. 2004 Mar;15(2):306-11. doi: 10.1016/j.nbd.2003.11.004. Neurobiol Dis. 2004. PMID: 15006700 Free article.

3

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

Oliveira G, Diogo L, Grazina M, Garcia P, Ataíde A, Marques C, Miguel T, Borges L, Vicente AM, Oliveira CR. Oliveira G, et al. Among authors: grazina m. Dev Med Child Neurol. 2005 Mar;47(3):185-9. doi: 10.1017/s0012162205000332. Dev Med Child Neurol. 2005. PMID: 15739723 Free article.

4

Mitochondrial DNA variants in a portuguese population of patients with Alzheimer's disease.

Grazina M, Silva F, Santana I, Pratas J, Santiago B, Oliveira M, Carreira I, Cunha L, Oliveira C. Grazina M, et al. Eur Neurol. 2005;53(3):121-4. doi: 10.1159/000085555. Epub 2005 Apr 28. Eur Neurol. 2005. PMID: 15860916 Free article.

5

Genetic basis of Alzheimer's dementia: role of mtDNA mutations.

Grazina M, Pratas J, Silva F, Oliveira S, Santana I, Oliveira C. Grazina M, et al. Genes Brain Behav. 2006;5 Suppl 2:92-107. doi: 10.1111/j.1601-183X.2006.00225.x. Genes Brain Behav. 2006. PMID: 16681804 Free article. Review.

6

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.

Correia C, Coutinho AM, Diogo L, Grazina M, Marques C, Miguel T, Ataíde A, Almeida J, Borges L, Oliveira C, Oliveira G, Vicente AM. Correia C, et al. Among authors: grazina m. J Autism Dev Disord. 2006 Nov;36(8):1137-40. doi: 10.1007/s10803-006-0138-6. J Autism Dev Disord. 2006. PMID: 17151801

7

Atypical presentation of Leber's hereditary optic neuropathy associated to mtDNA 11778G>A point mutation--A case report.

Grazina MM, Diogo LM, Garcia PC, Silva ED, Garcia TD, Robalo CB, Oliveira CR. Grazina MM, et al. Eur J Paediatr Neurol. 2007 Mar;11(2):115-8. doi: 10.1016/j.ejpn.2006.11.015. Epub 2007 Jan 24. Eur J Paediatr Neurol. 2007. PMID: 17254817

8

Pediatric mitochondrial respiratory chain disorders in the Centro region of Portugal.

Diogo L, Grazina M, Garcia P, Rebelo O, Veiga MA, Cuevas J, Vilarinho L, de Almeida IT, Oliveira CR. Diogo L, et al. Among authors: grazina m. Pediatr Neurol. 2009 May;40(5):351-6. doi: 10.1016/j.pediatrneurol.2008.11.012. Pediatr Neurol. 2009. PMID: 19380071

9

Mitochondrial-dependent apoptosis in Huntington's disease human cybrids.

Ferreira IL, Nascimento MV, Ribeiro M, Almeida S, Cardoso SM, Grazina M, Pratas J, Santos MJ, Januário C, Oliveira CR, Rego AC. Ferreira IL, et al. Among authors: grazina m. Exp Neurol. 2010 Apr;222(2):243-55. doi: 10.1016/j.expneurol.2010.01.002. Epub 2010 Jan 14. Exp Neurol. 2010. PMID: 20079354

10

Value of brain magnetic resonance imaging in mitochondrial respiratory chain disorders.

Diogo L, Cordeiro M, Garcia P, Fineza I, Moura C, Oliveira CR, Veiga M, Garcia T, Grazina M. Diogo L, et al. Among authors: grazina m. Pediatr Neurol. 2010 Mar;42(3):196-200. doi: 10.1016/j.pediatrneurol.2009.09.010. Pediatr Neurol. 2010. PMID: 20159429

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