Zobrazeno 1 - 5
of 5
pro vyhledávání: '"M. C. Ozelo"'
Autor:
F. L. B. Ferreira, M. P. Colella, S. S. Medina, C. Costa-Lima, M. M. L. Fiusa, L. N. G. Costa, F. A. Orsi, J. M. Annichino-Bizzacchi, K. Y. Fertrin, M. F. P. Gilberti, M. C. Ozelo, E. V. De Paula
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract The differential diagnosis of immune (ITP) and hereditary macrothrombocytopenia (HM) is key to patient management. The immature platelet fraction (IPF) represents the subset of circulating platelets with higher RNA content, and has been show
Externí odkaz:
https://doaj.org/article/6646c7dc9c244b0d87f194744b27fe23
Autor:
P, Poonnoose, J D A, Carneiro, A L, Cruickshank, M, El Ekiaby, R P, Perez Bianco, M C, Ozelo, N, De Bosch, M, Baghaipour, S L, Tien, A, Chuansumrit, E A, D'Amico, A, van Zyl, A, Sabour, M, Candela, J B S, Ricciardi, A, Ruiz-Sàez, R, Ravanbod, J C L, Lam, S, Jaovisidha, M L, Kavitha, S, Gibikote, N, Shyamkumar, A, Srivastava, P, Wongwerawattanakoon
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 23(4)
Patients and methods A longitudinal study was carried out in 255 children from 10 centres in nine developing countries over 5 years to assess the musculoskeletal outcome of children on episodic factor replacement. Outcome was documented by assessment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bec0281245e2842d97bed8995bf48966
https://pubmed.ncbi.nlm.nih.gov/28574179
https://pubmed.ncbi.nlm.nih.gov/28574179
Autor:
S M C, Vancine, S K, Picoli-Quaino, D S P, Costa, S A L, Montalvao, M C, Ozelo, J M, Annichino-Bizzacchi, E V, de Paula
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17(5)
For several years, coagulation has been implicated in the pathogenesis of sepsis. However, results from clinical trials with natural anticoagulants, as well as studies with knock-out mice for specific coagulation factors yielded conflicting results o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7ed96b07b0b4982cf3ecca133197bd6e
https://pubmed.ncbi.nlm.nih.gov/21682823
https://pubmed.ncbi.nlm.nih.gov/21682823
Autor:
V R, Arruda, W D, Belangero, M C, Ozelo, G B, Oliveira, R G, Pagnano, J B, Volpon, J M, Annichino-Bizzacchi
Publikováno v:
Journal of pediatric orthopedics. 19(1)
An inherited tendency to hypercoagulability has been suggested as a cause of vascular thrombosis resulting in Legg-Calvé-Perthes disease (LCPD). Here we carried out an investigation of the most common inherited risk factors for hypercoagulability in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a631e736c9ef1801704b476612c70e82
https://pubmed.ncbi.nlm.nih.gov/9890294
https://pubmed.ncbi.nlm.nih.gov/9890294
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