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The spectrum of mutations in Southern Spanish patients with von Willebrand disease.
Haemophilia. 2015 May;21(3):e240-e242. doi: 10.1111/hae.12649. Epub 2015 Feb 17.
Haemophilia. 2015.
PMID: 25689060
No abstract available.
Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect.
de la Morena-Barrio ME, Martínez-Martínez I, de Cos C, Wypasek E, Roldán V, Undas A, van Scherpenzeel M, Lefeber DJ, Toderici M, Sevivas T, España F, Jaeken J, Corral J, Vicente V.
de la Morena-Barrio ME, et al. Among authors: de cos c.
J Thromb Haemost. 2016 Aug;14(8):1549-60. doi: 10.1111/jth.13372. Epub 2016 Jun 29.
J Thromb Haemost. 2016.
PMID: 27214821
Free article.
Item in Clipboard
Successful immune tolerance induction with a plasma-derived FVIII concentrate and intravenous immunoglobulins in a pediatric patient with congenital severe hemophilia A and poor prognostic factors.
de Cos C, Rodríguez-Martorell J.
de Cos C, et al.
Blood Coagul Fibrinolysis. 2014 Jan;25(1):77-80. doi: 10.1097/MBC.0b013e328364f992.
Blood Coagul Fibrinolysis. 2014.
PMID: 24231694
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Successful discontinuation of eltrombopag after complete remission in patients with primary immune thrombocytopenia.
González-López TJ, Pascual C, Álvarez-Román MT, Fernández-Fuertes F, Sánchez-González B, Caparrós I, Jarque I, Mingot-Castellano ME, Hernández-Rivas JA, Martín-Salces M, Solán L, Beneit P, Jiménez R, Bernat S, Andrade MM, Cortés M, Cortti MJ, Pérez-Crespo S, Gómez-Núñez M, Olivera PE, Pérez-Rus G, Martínez-Robles V, Alonso R, Fernández-Rodríguez A, Arratibel MC, Perera M, Fernández-Miñano C, Fuertes-Palacio MA, Vázquez-Paganini JA, Gutierrez-Jomarrón I, Valcarce I, de Cabo E, Sainz A, Fisac R, Aguilar C, Paz Martínez-Badas M, Peñarrubia MJ, Calbacho M, de Cos C, González-Silva M, Coria E, Alonso A, Casaus A, Luaña A, Galán P, Fernández-Canal C, Garcia-Frade J, González-Porras JR.
González-López TJ, et al. Among authors: de cos c.
Am J Hematol. 2015 Mar;90(3):E40-3. doi: 10.1002/ajh.23900. Epub 2015 Jan 16.
Am J Hematol. 2015.
PMID: 25400215
Free article.
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Antithrombin Dublin (p.Val30Glu): a relatively common variant with moderate thrombosis risk of causing transient antithrombin deficiency.
Navarro-Fernández J, de la Morena-Barrio ME, Padilla J, Miñano A, Bohdan N, Águila S, Martínez-Martínez I, Sevivas TS, de Cos C, Fernández-Mosteirín N, Llamas P, Asenjo S, Medina P, Souto JC, Overvad K, Kristensen SR, Corral J, Vicente V.
Navarro-Fernández J, et al. Among authors: de cos c.
Thromb Haemost. 2016 Jul 4;116(1):146-54. doi: 10.1160/TH15-11-0871. Epub 2016 Apr 21.
Thromb Haemost. 2016.
PMID: 27098529
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Coexistence of three genetic risk factors in a Spanish thrombophilic family: Factor V Leiden, prothrombin 20210 and a new type I antithrombin deficiency.
Ordóñez A, de Cos C, Miñano A, Rodríguez J, Hernández-Espinosa D, Muñoz JA, González-Conejero R, Vicente V, Corral J.
Ordóñez A, et al. Among authors: de cos c.
Thromb Haemost. 2007 Jan;97(1):153-5.
Thromb Haemost. 2007.
PMID: 17200784
No abstract available.
Item in Clipboard
[Iron deficiency and pica].
Muñoz JA, Marcos J, Risueño CE, de Cos C, López R, Capote FJ, Martín MV, Gil JL.
Muñoz JA, et al. Among authors: de cos c.
Sangre (Barc). 1998 Feb;43(1):31-4.
Sangre (Barc). 1998.
PMID: 9580426
Spanish.
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Involvement of antifactor VIII autoantibodies specificity in the outcome of inhibitor eradication therapies in acquired hemophilia a patients.
Mingot-Castellano ME, Moret A, de Cos C, García-Candel F, Garrido R, González-Porras JR, López-Fernández MF, Quintana L, Rodríguez-González R, Marco P.
Mingot-Castellano ME, et al. Among authors: de cos c.
Blood Coagul Fibrinolysis. 2019 Apr;30(3):127-132. doi: 10.1097/MBC.0000000000000804.
Blood Coagul Fibrinolysis. 2019.
PMID: 30958453
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