Zobrazeno 1 - 10
of 94
pro vyhledávání: '"B Justiça"'
Publikováno v:
Acta Médica Portuguesa, Vol 12, Iss 7-11 (1999)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common erythrocyte enzymopathy, affecting over 400 million people worldwide. Portugal is a low prevalence country, but immigrants from endemic regions are common, particularly in the sou
Externí odkaz:
https://doaj.org/article/a46dcf5b0c2841d287ae92bdba9ce7a2
Autor:
M. F. López Fernández, J. Lasierra, B. Justiça, A. F. Villamor, J. L. Navarro, J. Batlle, A. Pardo, Michael Campos
Publikováno v:
Annals of Hematology. 68:111-115
Type IIA von Willebrand disease (vWD) is a heterogeneous disorder for which two different pathogenetic mechanisms have been proposed: increased proteolytic susceptibility of von Willebrand factor (vWF), and/or interference of its post-translational p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86defcf42826226b8045fd3296e6ca5e
https://doi.org/10.1007/bf01727414
https://doi.org/10.1007/bf01727414
Autor:
G, Porto, C S, Cardoso, V, Gordeuk, E, Cruz, J, Fraga, J, Areias, J C, Oliveira, F, Bravo, I T, Gangaidzo, A P, MacPhail, Z A, Gomo, V M, Moyo, G, Melo, C, Silva, B, Justiça, M, de Sousa
Publikováno v:
European journal of haematology. 67(2)
To identify a new marker of expression of disease, independent of HFE genotype in patients with hereditary haemochromatosis (HHC), the total peripheral blood lymphocyte counts were analysed according to iron status in two groups of subjects with HFE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::50a6529876b51c3a6fcdd6fdaa82957e
https://pubmed.ncbi.nlm.nih.gov/11722599
https://pubmed.ncbi.nlm.nih.gov/11722599
Publikováno v:
Haematologica. 86(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ce54456d93aad4b7915ebbdd617ac55
https://pubmed.ncbi.nlm.nih.gov/11224498
https://pubmed.ncbi.nlm.nih.gov/11224498
Publikováno v:
Hematological oncology. 15(2)
The bcl-2 oncogene has been involved in the genesis of various B-cell neoplasms by means of encoding for p26, an apoptosis suppressor oncoprotein. The expression of p26 in lymphoproliferative disorders of large granular lymphocytes (LDLGL), a group o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db8dd94a1ecd60f860504fcfe4cf079d
https://pubmed.ncbi.nlm.nih.gov/9375033
https://pubmed.ncbi.nlm.nih.gov/9375033
Autor:
G, Porto, C, Vicente, M A, Teixeira, O, Martins, J M, Cabeda, R, Lacerda, C, Goncalves, J, Fraga, G, Macedo, B M, Silva, H, Alves, B, Justiça, M, de Sousa
Publikováno v:
Hepatology (Baltimore, Md.). 25(2)
Hemochromatosis is a hereditary iron-overload disease linked to HLA. The clinical expression of hemochromatosis is influenced by sex and age. However, other factors must account for the notorious heterogeneity of expression of the disease independent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9469eee3379c22012209704cd9531c3a
https://pubmed.ncbi.nlm.nih.gov/9021953
https://pubmed.ncbi.nlm.nih.gov/9021953
Publikováno v:
Sangre. 41(5)
We describe a case of 27 year-old female presenting with Kikuchi-Fujimoto's disease whose diagnosis was based on histopathologic and immunophenotypic studies. The illness was characterized by fever, urinary tract infections, skin rash, polyarthritis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::394ab8e1db61aec33d8f9eb4665706f5
https://pubmed.ncbi.nlm.nih.gov/9026917
https://pubmed.ncbi.nlm.nih.gov/9026917
Autor:
M, Lima, M dos A, Teixeira, S, Morais, M, Cunha, J, Coutinho, L, Pinho, P, Ribeiro, B, Justiça
Publikováno v:
Sangre. 40(1)
To analyse the immunophenotype of acute leukaemia (AL) after myelodysplastic syndromes (MDS) (MDS-AL) and to compare the immunophenotypic profile of acute myeloblastic leukaemia (AML) secondary to MDS (MDS-AML) with that of "de novo"-AML.Twenty patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7169bfbe3222a3fcd21748168cc39b45
https://pubmed.ncbi.nlm.nih.gov/7716672
https://pubmed.ncbi.nlm.nih.gov/7716672
Publikováno v:
Sangre. 38(2)
To analyse the chromosomal abnormalities found at diagnosis in patients with malignant blood diseases.Between june 1988 and january 1992, cytogenetic studies were performed at the Cytogenetics Laboratory of the Abel Salazar Institute for Biomedical S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b6a4fb3678e768cf74cd2006658ab93
https://pubmed.ncbi.nlm.nih.gov/8516724
https://pubmed.ncbi.nlm.nih.gov/8516724
Publikováno v:
Gastroenterology. 108:A1115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64b89afd4a72ca044c7770676756e15e
https://doi.org/10.1016/0016-5085(95)28762-0
https://doi.org/10.1016/0016-5085(95)28762-0