Magalhães P - Search Results

1

High-resolution melting analysis for bird sexing: a successful approach to molecular sex identification using different biological samples.

Morinha F, Travassos P, Seixas F, Santos N, Sargo R, Sousa L, Magalhães P, Cabral JA, Bastos E. Morinha F, et al. Among authors: magalhaes p. Mol Ecol Resour. 2013 May;13(3):473-83. doi: 10.1111/1755-0998.12081. Epub 2013 Feb 25. Mol Ecol Resour. 2013. PMID: 23433263

2

Standard guidelines for the publication of telomere qPCR results in evolutionary ecology.

Morinha F, Magalhães P, Blanco G. Morinha F, et al. Among authors: magalhaes p. Mol Ecol Resour. 2020 May;20(3). doi: 10.1111/1755-0998.13152. Epub 2020 Mar 24. Mol Ecol Resour. 2020. PMID: 32133733 Review.

3

Efficient screening of the cystinuria-related C663T Slc3a1 nonsense mutation in Newfoundland dogs by denaturing high-performance liquid chromatography.

Matos AJ, Mascarenhas C, Magalhães P, Pinto JP. Matos AJ, et al. Among authors: magalhaes p. J Vet Diagn Invest. 2006 Jan;18(1):102-5. doi: 10.1177/104063870601800116. J Vet Diagn Invest. 2006. PMID: 16566266

4

Novel SPG3A and SPG4 mutations in dominant spastic paraplegia families.

Loureiro JL, Miller-Fleming L, Thieleke-Matos C, Magalhães P, Cruz VT, Coutinho P, Sequeiros J, Silveira I. Loureiro JL, et al. Among authors: magalhaes p. Acta Neurol Scand. 2009 Feb;119(2):113-8. doi: 10.1111/j.1600-0404.2008.01074.x. Epub 2008 Jul 29. Acta Neurol Scand. 2009. PMID: 18664244

5

Exclusion of mutations in the PRNP, JPH3, TBP, ATN1, CREBBP, POU3F2 and FTL genes as a cause of disease in Portuguese patients with a Huntington-like phenotype.

Costa MDC, Teixeira-Castro A, Constante M, Magalhães M, Magalhães P, Cerqueira J, Vale J, Passão V, Barbosa C, Robalo C, Coutinho P, Barros J, Santos MM, Sequeiros J, Maciel P. Costa MDC, et al. Among authors: magalhaes p, magalhaes m. J Hum Genet. 2006;51(8):645-651. doi: 10.1007/s10038-006-0001-9. Epub 2006 Jul 21. J Hum Genet. 2006. PMID: 16858508 Free PMC article.

6

Haplotype diversity and somatic instability in normal and expanded SCA8 alleles.

Martins S, Seixas AI, Magalhães P, Coutinho P, Sequeiros J, Silveira I. Martins S, et al. Among authors: magalhaes p. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):109-14. doi: 10.1002/ajmg.b.30235. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16184604

7

Molecular diagnosis of Huntington disease in Portugal: implications for genetic counselling and clinical practice.

Costa MC, Magalhães P, Ferreirinha F, Guimarães L, Januário C, Gaspar I, Loureiro L, Vale J, Garrett C, Regateiro F, Magalhães M, Sousa A, Maciel P, Sequeiros J. Costa MC, et al. Among authors: magalhaes p, magalhaes m. Eur J Hum Genet. 2003 Nov;11(11):872-8. doi: 10.1038/sj.ejhg.5201055. Eur J Hum Genet. 2003. PMID: 14571273

8

The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation.

Costa MDC, Magalhães P, Guimarães L, Maciel P, Sequeiros J, Sousa A. Costa MDC, et al. Among authors: magalhaes p. J Hum Genet. 2006;51(3):189-195. doi: 10.1007/s10038-005-0343-8. Epub 2005 Dec 22. J Hum Genet. 2006. PMID: 16372132

9

"COVID-19 in Trials and Tribulations" Project: A Self-Regulation-Based Support Response for Confined Families through Social Networks.

Pereira A, Magalhães P, Teixeira S, Núñez JC, Rosendo D, Mesquita S, Azevedo R, Martins JA, Fuentes S, Rosário P. Pereira A, et al. Among authors: magalhaes p. Int J Environ Res Public Health. 2022 Feb 8;19(3):1910. doi: 10.3390/ijerph19031910. Int J Environ Res Public Health. 2022. PMID: 35162931 Free PMC article.

10

Promoting School Engagement in Children with Cerebral Palsy: A Narrative Based Program.

Pereira A, Rosário P, Lopes S, Moreira T, Magalhães P, Núñez JC, Vallejo G, Sampaio A. Pereira A, et al. Among authors: magalhaes p. Int J Environ Res Public Health. 2019 Sep 27;16(19):3634. doi: 10.3390/ijerph16193634. Int J Environ Res Public Health. 2019. PMID: 31569711 Free PMC article. Clinical Trial.

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