Ferreira S - Search Results

1

Detection of prognostic significant translocations in childhood acute lymphoblastic leukaemia by one-step multiplex reverse transcription polymerase chain reaction.

Cerveira N, Ferreira S, Dória S, Veiga I, Ferreira F, Mariz JM, Marques M, Castedo S. Cerveira N, et al. Among authors: ferreira s, ferreira f. Br J Haematol. 2000 Jun;109(3):638-40. doi: 10.1046/j.1365-2141.2000.02051.x. Br J Haematol. 2000. PMID: 10886216 Free article.

2

Fabry disease: Detection of Alu-mediated exon duplication by NGS.

Farr M, Ferreira S, Al-Dilaimi A, Bögeholz S, Goesmann A, Kalinowski J, Knabbe C, Faber L, Oliveira JP, Rudolph V. Farr M, et al. Among authors: ferreira s. Mol Cell Probes. 2019 Jun;45:79-83. doi: 10.1016/j.mcp.2019.03.008. Epub 2019 Mar 29. Mol Cell Probes. 2019. PMID: 30936019

3

Preliminary data on the potential usefulness of B-type natriuretic peptide levels in predicting outcome after hospital discharge in patients with heart failure.

Bettencourt P, Ferreira S, Azevedo A, Ferreira A. Bettencourt P, et al. Among authors: ferreira s, ferreira a. Am J Med. 2002 Aug 15;113(3):215-9. doi: 10.1016/s0002-9343(02)01184-1. Am J Med. 2002. PMID: 12208380

4

Heart failure and sleep apnoea: to sleep perchance to dream.

Ferreira S, Winck J, Bettencourt P, Rocha-Goncalves F. Ferreira S, et al. Eur J Heart Fail. 2006 May;8(3):227-36. doi: 10.1016/j.ejheart.2005.07.013. Epub 2005 Sep 26. Eur J Heart Fail. 2006. PMID: 16185920 Free article. Review.

5

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Ferreira S, Costa C, Oliveira JP. Ferreira S, et al. Hum Genet. 2007 Jun;121(5):649. Hum Genet. 2007. PMID: 17879445 No abstract available.

6

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Ferreira S, Silva RS, Oliveira JP. Ferreira S, et al. Hum Genet. 2007 Jun;121(5):649. Hum Genet. 2007. PMID: 17879446 No abstract available.

7

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Ferreira S, Fontoura P, Guerreiro R, Oliveira JP. Ferreira S, et al. Hum Genet. 2007 Jun;121(5):649-50. Hum Genet. 2007. PMID: 17879447 No abstract available.

8

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant aretriopathy with subcortical infarcts and leukoencephalopathy.

Ferreira S, Malheiro F, Oliveira JP. Ferreira S, et al. Hum Genet. 2007 Jun;121(5):651-2. Hum Genet. 2007. PMID: 17879453 No abstract available.

9

N-terminal-pro-brain natriuretic peptide predicts outcome after hospital discharge in heart failure patients.

Bettencourt P, Azevedo A, Pimenta J, Friões F, Ferreira S, Ferreira A. Bettencourt P, et al. Among authors: ferreira s, ferreira a. Circulation. 2004 Oct 12;110(15):2168-74. doi: 10.1161/01.CIR.0000144310.04433.BE. Epub 2004 Sep 27. Circulation. 2004. PMID: 15451800

10

Comparative analysis of undernutrition screening and diagnostic tools as predictors of hospitalisation costs.

Guerra RS, Sousa AS, Fonseca I, Pichel F, Restivo MT, Ferreira S, Amaral TF. Guerra RS, et al. Among authors: ferreira s. J Hum Nutr Diet. 2016 Apr;29(2):165-73. doi: 10.1111/jhn.12288. Epub 2014 Dec 23. J Hum Nutr Diet. 2016. PMID: 25532556

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