Ferreira M - Search Results

1

Progressive cavitating leukoencephalopathy associated with respiratory chain complex I deficiency and a novel mutation in NDUFS1.

Ferreira M, Torraco A, Rizza T, Fattori F, Meschini MC, Castana C, Go NE, Nargang FE, Duarte M, Piemonte F, Dionisi-Vici C, Videira A, Vilarinho L, Santorelli FM, Carrozzo R, Bertini E. Ferreira M, et al. Neurogenetics. 2011 Feb;12(1):9-17. doi: 10.1007/s10048-010-0265-2. Epub 2011 Jan 4. Neurogenetics. 2011. PMID: 21203893

2

Relative frequency of known causes of multiple mtDNA deletions: two novel POLG mutations.

Ferreira M, Evangelista T, Almeida LS, Martins J, Macario MC, Martins E, Moleirinho A, Azevedo L, Vilarinho L, Santorelli FM. Ferreira M, et al. Neuromuscul Disord. 2011 Jul;21(7):483-8. doi: 10.1016/j.nmd.2011.03.011. Epub 2011 May 7. Neuromuscul Disord. 2011. PMID: 21550804

3

Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA.

Azevedo O, Vilarinho L, Almeida F, Ferreira F, Guardado J, Ferreira M, Lourenço A, Medeiros R, Almeida J. Azevedo O, et al. Among authors: ferreira m, ferreira f. Cardiology. 2010;115(1):71-4. doi: 10.1159/000252811. Epub 2009 Oct 27. Cardiology. 2010. PMID: 19864902

4

SANDO: two novel mutations in POLG1 gene.

Gago MF, Rosas MJ, Guimarães J, Ferreira M, Vilarinho L, Castro L, Carpenter S. Gago MF, et al. Among authors: ferreira m. Neuromuscul Disord. 2006 Aug;16(8):507-9. doi: 10.1016/j.nmd.2006.05.016. Epub 2006 Aug 21. Neuromuscul Disord. 2006. PMID: 16919951

5

Identification of novel L2HGDH gene mutations and update of the pathological spectrum.

Vilarinho L, Tafulo S, Sibilio M, Kok F, Fontana F, Diogo L, Venâncio M, Ferreira M, Nogueira C, Valongo C, Parenti G, Amorim A, Azevedo L. Vilarinho L, et al. Among authors: ferreira m. J Hum Genet. 2010 Jan;55(1):55-8. doi: 10.1038/jhg.2009.110. Epub 2009 Nov 13. J Hum Genet. 2010. PMID: 19911013

6

Salt intake and risk of gastric intestinal metaplasia: systematic review and meta-analysis.

Dias-Neto M, Pintalhao M, Ferreira M, Lunet N. Dias-Neto M, et al. Among authors: ferreira m. Nutr Cancer. 2010;62(2):133-47. doi: 10.1080/01635580903305391. Nutr Cancer. 2010. PMID: 20099187 Review.

7

Diets supplemented with Saccharina latissima influence the expression of genes related to lipid metabolism and oxidative stress modulating rainbow trout (Oncorhynchus mykiss) fillet composition.

Ferreira M, Larsen BK, Granby K, Cunha SC, Monteiro C, Fernandes JO, Nunes ML, Marques A, Dias J, Cunha I, Castro LFC, Valente LMP. Ferreira M, et al. Food Chem Toxicol. 2020 Jun;140:111332. doi: 10.1016/j.fct.2020.111332. Epub 2020 Apr 17. Food Chem Toxicol. 2020. PMID: 32305409 Free article.

8

Could Commercial Formulations Replace Individualized Prescription in Pediatric Home Parenteral Nutrition?

Ferreira M, Guerra P, Ferreras C, Espinheira MDC, Trindade E, Dias JA. Ferreira M, et al. J Pediatr Gastroenterol Nutr. 2021 Oct 1;73(4):548-554. doi: 10.1097/MPG.0000000000003187. J Pediatr Gastroenterol Nutr. 2021. PMID: 34546996

9

Awake Craniotomy for Eloquent Brain Arteriovenous Malformations: A Systematic Review and Individual Patient Data Meta-Analysis.

Semione G, de Oliveira Almeida G, Lepine HL, Borges PGL, Lima Larcipretti AL, Ferreira MY, Palavani LB, Belfort M, Oliveira LB, Andreão FF, Baldissera GF, Bocanegra-Becerra JE, Santana MFP, Bertani R, Lawton MT, Figueiredo EG. Semione G, et al. Among authors: ferreira my. World Neurosurg. 2024 Dec 24:123609. doi: 10.1016/j.wneu.2024.123609. Online ahead of print. World Neurosurg. 2024. PMID: 39725290 Review.

10

Correction: Large Clostridial Toxins: A Brief Review and Insights into Antigen Design for Veterinary Vaccine Development.

Rodrigues Rodrigues R, Alves MLF, Bilhalva MA, Kremer FS, Junior CM, Ferreira MRA, Galvão CC, Quatrin PHDN, Conceição FR. Rodrigues Rodrigues R, et al. Among authors: ferreira mra. Mol Biotechnol. 2024 Dec 24. doi: 10.1007/s12033-024-01352-x. Online ahead of print. Mol Biotechnol. 2024. PMID: 39718703 No abstract available.

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