Zobrazeno 1 - 10
of 62
pro vyhledávání: '"N. De Bosch"'
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
Akademický článek
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Autor:
F H, Herrmann, K, Wulff, G, Auerswald, S, Schulman, J, Astermark, A, Batorova, W, Kreuz, H, Pollmann, A, Ruiz-Saez, N, De Bosch, L, Salazar-Sanchez, A, Boadas
Publikováno v:
Haemophilia. 15:267-280
The congenital FVII deficiency (FVIID) is a rare haemorrhagic disorder with an autosomal recessive pattern of inheritance. Data on phenotype and the genotype from 717 subjects in Central Europe (six countries), Latin America (Costa Rica, Venezuela) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f2a273f310b43fbb7308c8720d30981
https://doi.org/10.1111/j.1365-2516.2008.01910.x
https://doi.org/10.1111/j.1365-2516.2008.01910.x
Publikováno v:
Tissue Antigens. 25:216-219
Twenty-eight unrelated hemophilia A patients, seven of them with anti-factor VIII antibodies were typed for HLA-A, B, C antigens and 25 of them for HLA-DR. The results show a significant difference in HLA-DR4 frequency between hemophiliacs with antib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::146b1035b785723096353d0ec6f28951
https://doi.org/10.1111/j.1399-0039.1985.tb00440.x
https://doi.org/10.1111/j.1399-0039.1985.tb00440.x
Publikováno v:
Annals of Hematology. 86:879-885
The haemostatic components of venom from the genus Porthidium has been poorly studied, although it is known that severe manifestations occur when humans are envenomed, which include invasive oedema and disseminated ecchymosis. The effects of venom on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15cb8dad4ed86b3e201a7187a11f2fe7
https://doi.org/10.1007/s00277-007-0354-y
https://doi.org/10.1007/s00277-007-0354-y
Autor:
Francesco Baudo, Javier Batlle, Jcj Eikenboom, Giancarlo Castaman, Francesco Rodeghiero, Augusto B. Federici, N. de Bosch, A. Cappelletti, Alberto Tosetto, P Casana, Stefan Lethagen, S. Linari, Arun Srivastava
Publikováno v:
Journal of Thrombosis and Haemostasis. 3:2619-2626
Objective: The aim of this study was the validation of the criteria defining a significant mucocutaneous-bleeding history in type 1 von Willebrand disease (VWD). Subjects and methods: To avoid selection bias, 42 obligatory carriers (OC) of type 1 VWD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6451add0a0a86021422e74b0c5a1e5e2
https://doi.org/10.1111/j.1538-7836.2005.01663.x
https://doi.org/10.1111/j.1538-7836.2005.01663.x
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Autor:
R. Ocazionez, Jorge L. Muñoz-Jordán, Lee Gehrke, Adriano Mondini, Gilberto A. Santiago, P.F. Vasconcelos, E. V. da Silva, Matthew R. Henn, Elliot J. Lefkowitz, Bruce W. Birren, N. de Bosch, Maurício Lacerda Nogueira, Irene Bosch, Guillermo Comach, Niall J. Lennon, Kris Xhaja, Brett E. Pickett, Diane J. Schmidt, Aniuska Becerra, Daría Elena Camacho, Kamran Rizzolo
Publikováno v:
Repositório Digital do Instituto Evandro Chagas (Patuá)
Instituto Evandro Chagas (IEC)
instacron:IEC
PMC
Instituto Evandro Chagas (IEC)
instacron:IEC
PMC
University of Massachusetts Medical School. Worcester, MA, USA. University of Alabama at Birmingham. Birmingham, Al, USA. Biomed, Universidad de Carabobo. Maracay, Venezuela. Biomed, Universidad de Carabobo. Maracay, Venezuela. University of Massachu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f3c2e845d0e3e811c248833c927da66
https://pubmed.ncbi.nlm.nih.gov/21964598
https://pubmed.ncbi.nlm.nih.gov/21964598
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17(5)
Haemophilia A is caused by mutations in the gene encoding coagulation factor VIII (FVIII). In severe Haemophilia A (sHA), two inversions are responsible for approximately 50% of the genetic alterations (intron 22 and intron 1 inversions). The other m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd3d2c50dd9433a260c8670d7d1d9441
https://pubmed.ncbi.nlm.nih.gov/21371196
https://pubmed.ncbi.nlm.nih.gov/21371196
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 6
Most of the world's haemophilia population lives in countries with few medical or financial resources. As such, they cannot easily obtain viral-inactivated clotting product. Many patients are treated with cryoprecipitate made from locally supplied bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ebdf1f06891bb72102dfe774263cde4
https://pubmed.ncbi.nlm.nih.gov/10982279
https://pubmed.ncbi.nlm.nih.gov/10982279