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Registros recuperados: 3
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Central venous access through the external jugular vein in children submitted to bone marrow transplantation BABT
Godoy,José Luiz de; Otta,Edson Keity; Miyazaki,Ricardo Atsumori; Bitencourt,Marco Antonio; Pasquini,Ricardo.
Establishment of long-term central venous access is a sine qua non step for bone marrow transplantation in children. Most frequently, long-term central venous access has been obtained via blind percutaneous cannulation of subclavian and internal jugular veins or via internal jugular vein cutdown. In order to avoid some potential minor and major complications associated with the subclavian or internal jugular approaches, the authors describe an easy, simple and safe method for central venous access through an external jugular vein cutdown that should be of interest to readers involved in the field of bone marrow transplantation. It should be also considered for children as well as adults needing central venous access via an external catheter - or totally...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Central venous access; External jugular vein; Bone marrow transplantation; Catheter.
Ano: 2005 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132005000100007
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Cytogenetic study of Brazilian patients with myelodysplastic syndrome (MDS) Genet. Mol. Biol.
Borgonovo,Tamara; Ribeiro,Enilze M.S.F.; Cornélio,Déborah Afonso; Schmid-Braz,Ana Teresa; Jamur,Valderez Ravaglio; Wuicik,Lismeri; Veiga,Loraine Beatriz Acosta; Ehmke,Néria A. Maia; Pasquini,Ricardo; Cavalli,Iglenir João.
Bone marrow cytogenetic studies were performed on 93 patients with primary myelodysplastic syndrome (MDS) diagnosed at the Clinical Hospital of the Federal University of Paraná, Brazil. Chromosomal alterations were observed in 69% of the patients. Monosomy of chromosome 7, deletions of 7q, 5q, 12p and 20q, rearrangements of 11q23 and trisomies of chromosomes 8 and 21 were the most frequent abnormalities observed. Among adult patients the most frequent aberrations were rearrangements of 11q23 and 12p deletions. In the pediatric group, 5q deletions and monosomy of chromosome 7 were the most common alterations.
Tipo: Info:eu-repo/semantics/article Palavras-chave: Hematological disorders; Myelodysplasias; Cancer cytogenetics.
Ano: 2005 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572005000500002
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Invasive aspergillosis in hematopoietic stem cell transplant recipients: a retrospective analysis BJID
Carvalho-Dias,Viviane Maria Hessel; Sola,Caroline Bonamin Santos; Cunha,Clóvis Arns da; Shimakura,Sílvia Emiko; Pasquini,Ricardo; Queiroz-Telles,Flávio de.
Invasive aspergillosis (IA) currently is an important cause of mortality in subjects undergoing hematopoietic stem cell transplants (HSCT) and is also an important cause of opportunistic respiratory and disseminated infections in other types of immunocompromised patients. We examined the medical records of 24 cases of proven and probable invasive aspergillosis (IA) at the Hospital de Clinicas of the Federal University of Parana, Brazil, from January 1996 to October 2006. During this period occurred a mean of 2.2 cases per year or 3.0 cases per 100 HSTC transplants. There was a significant relationship between structural changes in the bone marrow transplant (BMT) Unit and the occurrence of IA cases (p=0.034, relative risk (RR) = 2.47). Approximately 83% of...
Tipo: Info:eu-repo/semantics/article Palavras-chave: Invasive aspergillosis; Transplant recipients; Immunocompromised.
Ano: 2008 URL: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702008000500008
Registros recuperados: 3
Primeira ... 1 ... Última
 

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