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Items: 14


Oral anticoagulant therapy does not modify the bleeding pattern associated with the levonorgestrel-releasing intrauterine system in women with thrombophilia and/or a history of thrombosis.

Braga GC, Brito MB, Ferriani RA, Oliveira LC, Garcia AA, Pintão MC, Vieira CS.

Contraception. 2014 Jan;89(1):48-53. doi: 10.1016/j.contraception.2013.06.012. Epub 2013 Jul 12.


Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study.

Pintao MC, Ribeiro DD, Bezemer ID, Garcia AA, de Visser MC, Doggen CJ, Lijfering WM, Reitsma PH, Rosendaal FR.

Blood. 2013 Oct 31;122(18):3210-9. doi: 10.1182/blood-2013-04-499335. Epub 2013 Sep 6.


Analysis of the storage and secretion of von Willebrand factor in blood outgrowth endothelial cells derived from patients with von Willebrand disease.

Wang JW, Bouwens EA, Pintao MC, Voorberg J, Safdar H, Valentijn KM, de Boer HC, Mertens K, Reitsma PH, Eikenboom J.

Blood. 2013 Apr 4;121(14):2762-72. doi: 10.1182/blood-2012-06-434373. Epub 2013 Feb 20.


High levels of protein C are determined by PROCR haplotype 3.

Pintao MC, Roshani S, de Visser MC, Tieken C, Tanck MW, Wichers IM, Meijers JC, Rosendaal FR, Middeldorp S, Reitsma PH.

J Thromb Haemost. 2011 May;9(5):969-76. doi: 10.1111/j.1538-7836.2011.04256.x.


Error in body weight estimation leads to inadequate parenteral anticoagulation.

dos Reis Macedo LG, de Oliveira L, Pintão MC, Garcia AA, Pazin-Filho A.

Am J Emerg Med. 2011 Jul;29(6):613-7. doi: 10.1016/j.ajem.2010.01.006. Epub 2010 Apr 2.


Novel human pathological mutations. Gene symbol: PROS1. Disease: Protein S deficiency.

Pintao M, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH.

Hum Genet. 2010 Jan;127(1):121. No abstract available.


Incidence and risk factors of aplastic anemia in Latin American countries: the LATIN case-control study.

Maluf E, Hamerschlak N, Cavalcanti AB, Júnior AA, Eluf-Neto J, Falcão RP, Lorand-Metze IG, Goldenberg D, Santana CL, Rodrigues Dde O, Passos LN, Rosenfeld LG, Pitta M, Loggetto S, Ribeiro AA, Velloso ED, Kondo AT, Coelho EO, Pintão MC, de Souza HM, Borbolla JR, Pasquini R.

Haematologica. 2009 Sep;94(9):1220-6. doi: 10.3324/haematol.2008.002642.


Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Pintao MC, Garcia AA, Borgel D, Alhenc-Gelas M, Spek CA, de Visser MC, Gandrille S, Reitsma PH.

Hum Genet. 2009 Sep;126(3):449-56. doi: 10.1007/s00439-009-0687-9. Epub 2009 May 23.


Determination of P-glycoprotein, MDR-related protein 1, breast cancer resistance protein, and lung-resistance protein expression in leukemic stem cells of acute myeloid leukemia.

de Figueiredo-Pontes LL, Pintão MC, Oliveira LC, Dalmazzo LF, Jácomo RH, Garcia AB, Falcão RP, Rego EM.

Cytometry B Clin Cytom. 2008 May;74(3):163-8. doi: 10.1002/cyto.b.20403.


Use of the etonogestrel-releasing implant is associated with hypoactivation of the coagulation cascade.

Vieira CS, Ferriani RA, Garcia AA, Pintão MC, Azevedo GD, Gomes MK, Silva-de-Sá MF.

Hum Reprod. 2007 Aug;22(8):2196-201. Epub 2007 Jun 13.


Mitochondrial DNA sequence variation in single cells from leukemia patients.

Yao YG, Ogasawara Y, Kajigaya S, Molldrem JJ, Falcão RP, Pintão MC, McCoy JP Jr, Rizzatti EG, Young NS.

Blood. 2007 Jan 15;109(2):756-62. Epub 2006 Aug 31.


Asynchronous expression of myeloid antigens in leukemic cells in a PML/RARalpha transgenic mouse model.

Santana BA, Pintão MC, Abreu e Lima RS, Scheucher PS, Santos GA, Garcia AB, Falcão RP, Rego EM.

Braz J Med Biol Res. 2006 May;39(5):615-20. Epub 2006 Apr 20.


Lack of mutations in the human telomerase RNA component (hTERC) gene in Fanconi's anemia.

Calado RT, Pintão MC, Rocha V, Falcão RP, Bitencourt MA, Silva WA Jr, Gluckman E, Pasquini R, Zago MA.

Haematologica. 2004 Aug;89(8):1012-3.


Aplastic anaemia and telomerase RNA mutations.

Calado RT, Pintão MC, Silva WA Jr, Falcão RP, Zago MA.

Lancet. 2002 Nov 16;360(9345):1608. No abstract available.


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