Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Renée Leonor Crisp"'
Autor:
Nicolás Ambrosis, Pablo Martin Aispuro, Keila Belhart, Daniela Bottero, Renée Leonor Crisp, María Virginia Dansey, Magali Gabrielli, Oscar Filevich, Valeria Genoud, Alejandra Giordano, Min Chih Lin, Anibal Lodeiro, Felipe Marceca, Nicolás Pregi, Federico Remes Lenicov, Luciana Rocha-Viegas, Erika Rudi, Guillermo Solovey, Eugenia Zurita, Adali Pecci, Roberto Etchenique, Daniela Hozbor
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Background: The high COVID-19 dissemination rate demands active surveillance to identify asymptomatic, presymptomatic, and oligosymptomatic (APO) SARS-CoV-2-infected individuals. This is of special importance in communities inhabiting closed or semi-
Externí odkaz:
https://doaj.org/article/49c33ef1385c4d6ca2c9ed81d065b17a
Autor:
Nicolás Ambrosis, Pablo Martin Aispuro, Keila Belhart, Daniela Bottero, Renée Leonor Crisp, María Virginia Dansey, Magali Gabrielli, Oscar Filevich, Valeria Genoud, Alejandra Giordano, Min Chih Lin, Anibal Lodeiro, Felipe Marceca, Nicolás Pregi, Federico Remes Lenicov, Luciana Rocha-Viegas, Erika Rudi, Guillermo Solovey, Eugenia Zurita, Adali Pecci, Roberto Etchenique, Daniela Hozbor
Publikováno v:
Frontiers in Medicine
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Frontiers in Medicine, Vol 8 (2021)
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Frontiers in Medicine, Vol 8 (2021)
Background: The high COVID-19 dissemination rate demands active surveillance to identify asymptomatic, presymptomatic, and oligosymptomatic (APO) SARS-CoV-2-infected individuals. This is of special importance in communities inhabiting closed or semi-
Publikováno v:
Archivos argentinos de pediatria. 113(2)
Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group in
Publikováno v:
Archivos argentinos de pediatria. 113(1)
Hereditary spherocytosis is the most frequent hereditary anemia excluding beta thalassemia in Argentina. Historical, demographic, genetic and pathogenic aspects of the disease are reviewed, and confirmatory laboratory tests are described. Special cha