Carreira IM - Search Results

1

MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report.

Othman MA, Melo JB, Carreira IM, Rincic M, Alhourani E, Wilhelm K, Gruhn B, Glaser A, Liehr T. Othman MA, et al. Among authors: carreira im. Oncol Rep. 2015 Feb;33(2):625-30. doi: 10.3892/or.2014.3624. Epub 2014 Nov 25. Oncol Rep. 2015. PMID: 25435396

2

Two new cases of de novo small supernumerary marker chromosomes (sSMC) detected at prenatal diagnosis.

Jardim A, Melo JB, Matoso E, Pires LM, Ramos L, Carreira IM. Jardim A, et al. Among authors: carreira im. Prenat Diagn. 2007 Apr;27(4):380-1. doi: 10.1002/pd.1650. Prenat Diagn. 2007. PMID: 17393554 Free article. No abstract available.

3

Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18.

Carreira IM, Mascarenhas A, Matoso E, Couceiro AB, Ramos L, Dufke A, Mazauric M, Stressig R, Kosyakova N, Melo JB, Liehr T. Carreira IM, et al. J Histochem Cytochem. 2007 Nov;55(11):1123-8. doi: 10.1369/jhc.7A7244.2007. Epub 2007 Jun 26. J Histochem Cytochem. 2007. PMID: 17595336 Free PMC article.

4

First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.

Mascarenhas A, Matoso E, Saraiva J, Tönnies H, Gerlach A, Julião MJ, Melo JB, Carreira IM. Mascarenhas A, et al. Among authors: carreira im. Cytogenet Genome Res. 2008;121(3-4):293-7. doi: 10.1159/000138901. Epub 2008 Aug 29. Cytogenet Genome Res. 2008. PMID: 18758175

5

Analytical approaches toward successful human cell metabolome studies by NMR spectroscopy.

Duarte IF, Marques J, Ladeirinha AF, Rocha C, Lamego I, Calheiros R, Silva TM, Marques MP, Melo JB, Carreira IM, Gil AM. Duarte IF, et al. Among authors: carreira im. Anal Chem. 2009 Jun 15;81(12):5023-32. doi: 10.1021/ac900545q. Anal Chem. 2009. PMID: 19462963 Free article.

6

Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy.

Carreira IM, Melo JB, Rodrigues C, Backx L, Vermeesch J, Weise A, Kosyakova N, Oliveira G, Matoso E. Carreira IM, et al. Mol Cytogenet. 2009 Aug 4;2:16. doi: 10.1186/1755-8166-2-16. Mol Cytogenet. 2009. PMID: 19653912 Free PMC article.

7

Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.

Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM. Melo JB, et al. Among authors: carreira im. Cytogenet Genome Res. 2009;125(2):109-14. doi: 10.1159/000227834. Epub 2009 Aug 31. Cytogenet Genome Res. 2009. PMID: 19729913

8

X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.

Ferreira SI, Matoso E, Pinto M, Almeida J, Liehr T, Melo JB, Carreira IM. Ferreira SI, et al. Among authors: carreira im. Mol Cytogenet. 2010 Jul 20;3:14. doi: 10.1186/1755-8166-3-14. Mol Cytogenet. 2010. PMID: 20646274 Free PMC article.

9

Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.

Melo JB, Backx L, Vermeesch JR, Santos HG, Sousa AC, Kosyakova N, Weise A, von Eggeling F, Liehr T, Carreira IM. Melo JB, et al. Among authors: carreira im. J Appl Genet. 2011 May;52(2):193-200. doi: 10.1007/s13353-011-0035-3. Epub 2011 Mar 25. J Appl Genet. 2011. PMID: 21437654 Review.

10

Critical region in 2q31.2q32.3 deletion syndrome: Report of two phenotypically distinct patients, one with an additional deletion in Alagille syndrome region.

Ferreira SI, Matoso E, Venâncio M, Saraiva J, Melo JB, Carreira IM. Ferreira SI, et al. Among authors: carreira im. Mol Cytogenet. 2012 May 2;5(1):25. doi: 10.1186/1755-8166-5-25. Mol Cytogenet. 2012. PMID: 22550961 Free PMC article.

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