Morais S - Search Results

1

Aggressive Neuroblastoma in a Pediatric Patient with Severe Hemophilia A.

Costa L, Couto ME, Moutinho J, Ferreira AM, Costa E, Roncon S, Santos LL, Cruz E, Morais S. Costa L, et al. Among authors: morais s. Pediatr Rep. 2021 Mar 8;13(1):125-130. doi: 10.3390/pediatric13010018. Pediatr Rep. 2021. PMID: 33800180 Free PMC article.

2

Neonatal Hemophilia: A Rare Presentation.

Ferreira N, Proença E, Godinho C, Oliveira D, Guedes A, Morais S, Carvalho C. Ferreira N, et al. Among authors: morais s. Pediatr Rep. 2015 Dec 21;7(4):6338. doi: 10.4081/pr.2015.6338. eCollection 2015 Dec 9. Pediatr Rep. 2015. PMID: 26734126 Free PMC article.

3

αIIbβ3 variants in ten families with autosomal dominant macrothrombocytopenia: Expanding the mutational and clinical spectrum.

Morais S, Oliveira J, Lau C, Pereira M, Gonçalves M, Monteiro C, Gonçalves AR, Matos R, Sampaio M, Cruz E, Freitas I, Santos R, Lima M. Morais S, et al. PLoS One. 2020 Dec 4;15(12):e0235136. doi: 10.1371/journal.pone.0235136. eCollection 2020. PLoS One. 2020. PMID: 33276370 Free PMC article.

4

[Guidelines on: COVID-19 Vaccine Induced Thrombosis, Bleeding, and Thrombocytopenia].

Morais S, Cruz E. Morais S, et al. Acta Med Port. 2021 Aug 31;34(9):625-629. doi: 10.20344/amp.16602. Epub 2021 Jun 18. Acta Med Port. 2021. PMID: 34147137 Free article. Portuguese.

5

CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in RASGRP2.

Morais S, Pereira M, Lau C, Gonçalves A, Monteiro C, Gonçalves M, Oliveira J, Moreira L, Cruz E, Santos R, Lima M. Morais S, et al. Int J Mol Sci. 2021 Nov 17;22(22):12423. doi: 10.3390/ijms222212423. Int J Mol Sci. 2021. PMID: 34830306 Free PMC article.

6

Inflammatory and Hemostatic Markers in COVID-19 Patients with Arterial Thrombosis Are Significantly Lower at Hospital Admission than in COVID-19 Patients without Thrombosis.

de Oliveira M, Cubal F, Coutinho M, Pereira M, Cruz E, Morais S. de Oliveira M, et al. Among authors: morais s. Viruses. 2022 Oct 24;14(11):2330. doi: 10.3390/v14112330. Viruses. 2022. PMID: 36366428 Free PMC article.

7

HFE mutations in the pathobiology of hemophilic arthropathy.

Cruz E, Porto G, Morais S, Campos M, de Sousa M. Cruz E, et al. Among authors: morais s. Blood. 2005 Apr 15;105(8):3381-2. doi: 10.1182/blood-2004-11-4342. Blood. 2005. PMID: 15802547 Free article. No abstract available.

8

Parkin truncating variants result in a loss-of-function phenotype.

Santos M, Morais S, Pereira C, Sequeiros J, Alonso I. Santos M, et al. Among authors: morais s. Sci Rep. 2019 Nov 6;9(1):16150. doi: 10.1038/s41598-019-52534-6. Sci Rep. 2019. PMID: 31695088 Free PMC article.

9

Advances in the genotyping of thrombosis genetic risk factors: clinical and laboratory implications.

Cabeda JM, Pereira M, Oliveira JM, Estevinho A, Pereira I, Morais S, Justiça B, Campos M. Cabeda JM, et al. Among authors: morais s. Pathophysiol Haemost Thromb. 2002 Sep-Dec;32(5-6):235-40. doi: 10.1159/000073572. Pathophysiol Haemost Thromb. 2002. PMID: 13679648 Free article. Review.

10

Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal.

Garcia LC, Breillat C, Lima M, Combrié R, Morais S, Teixera Mdos A, Campos M, Justica B, Nurden AT. Garcia LC, et al. Among authors: morais s. Platelets. 2004 Feb;15(1):15-22. doi: 10.1080/0953710032000158754. Platelets. 2004. PMID: 14985172

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