Zobrazeno 1 - 10
of 29
pro vyhledávání: '"SILVIA EANDI EBERLE"'
Autor:
SILVIA EANDI EBERLE, ALEJANDRO CHAVES, CAROLINA PEPE, MARIA PAULA DIUZEIDE, DIEGO FERNANDEZ, FLORENICA NOVELLO, VANESA AVALOS GOMEZ
Publikováno v:
Revista Hematología. 26:97-100
La metahemoglobinemia es una condición caracterizada por la presencia de altas concentraciones de metahemoglobina en sangre, la cual es incapaz de liberar oxígeno a los tejidos. Es una entidad poco frecuente, con baja sospecha diagnóstica, y puede
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5771399574e53200cec337c08a624184
https://doi.org/10.48057/hematologa.v26i2.427
https://doi.org/10.48057/hematologa.v26i2.427
Autor:
Fernando Aguirre, Silvia Eandi Eberle, Agustina Albero, Carolina Pepe, Lucas A. Defelipe, Luciana Aizpurua, Berenice Milanesio, Vanesa Avalos Gómez, Adrian Turjanski, Maria Paula Dieuzeide, Paola Bianchi, Aurora Feliu-Torres, Diego Fernandez, Elisa Fermo, Alejandro Chaves
Publikováno v:
Clinical biochemistry. 91
Background Pyruvate kinase deficiency (PKD) is a rare recessive congenital hemolytic anemia caused by mutations in the PKLR gene. The disease shows a marked variability in clinical expression. We studied the molecular features of nine unrelated Argen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc42232338a88d7076b5a19d3c421381
https://pubmed.ncbi.nlm.nih.gov/33631127
https://pubmed.ncbi.nlm.nih.gov/33631127
Autor:
Alejandro Chaves, Luciana Aizpurua, Silvia Eandi Eberle, Vanesa Avalos Gómez, Fernando Aguirre, Agustina Albero, Maria Paula Dieuzeide, Berenice Milanesio, Aurora Feliu-Torres, Diego Fernandez, Carolina Pepe
Publikováno v:
Clinical Biochemistry. 81:63-64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2fa968347f371a1680fbeaa30d96bbb
https://doi.org/10.1016/j.clinbiochem.2020.04.007
https://doi.org/10.1016/j.clinbiochem.2020.04.007
Autor:
Diego Fernandez, Analía Kinen, Silvia Eandi Eberle, Fernando Aguirre, Berenice Milanesio, Aurora Feliú Torres, Vanesa Avalos Gómez, Carolina Pepe
Publikováno v:
Archivos Argentinos de Pediatria. 117
Hereditary xerocytosis is a rare disorder caused by defects of red blood cell permeability that are characterized by hemolytic anemia of variable degree and iron overload. Diagnosis is usually late and confused with other hemolytic anemias, which can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3b816395b259002cbec9289754efed2
https://doi.org/10.5546/aap.2019.e684
https://doi.org/10.5546/aap.2019.e684
Autor:
Lilián Díaz, Silvia Eandi Eberle, Carolina Cervio, Berenice Milanesio, Gabriela Sciuccati, Mariana Bonduel, Diego Fernandez, Aurora Feliú Torres, Vanesa Avalos Gómez, Andrea Candás, Alejandro Chaves, Fernando Aguirre, Carolina Pepe
Publikováno v:
Archivos Argentinos de Pediatria. 117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6565561cf75ac75bc21a31376b8a87ae
https://doi.org/10.5546/aap.2019.267
https://doi.org/10.5546/aap.2019.267
Autor:
Silvia, Eandi Eberle, Carolina, Pepe, Fernando, Aguirre, Berenice, Milanesio, Diego, Fernández, Vanesa, Ávalos Gómez, Analía, Kinen, Aurora, Feliu Torres
Publikováno v:
Archivos argentinos de pediatria. 117(6)
Hereditary xerocytosis is a rare disorder caused by defects of red blood cell permeability that are characterized by hemolytic anemia of variable degree and iron overload. Diagnosis is usually late and confused with other hemolytic anemias, which can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::789a7a71f6e8d0480482861e17eabf21
https://pubmed.ncbi.nlm.nih.gov/31758911
https://pubmed.ncbi.nlm.nih.gov/31758911
Autor:
Silvia Eandi-Eberle, Patricia L. Rubio, Mariela C. Coccé, Sophia Polychronopoulou, Vassilios Papadakis, Stefanos I. Papadhimitriou, George Paterakis, Marta S. Gallego, Cristina N. Alonso, Loizos Petrikkos, Andrea Bernasconi, Maria S. Felice, Jorge Rossi, Adrian P. Mansini, E.O. Sajaroff, Maria Ampatzidou
Publikováno v:
Leukemia & Lymphoma. 57:2289-2297
The association between mature-B phenotype and MLL abnormalities in acute lymphoblastic leukemia (ALL) is a very unusual finding; only 14 pediatric cases have been reported so far. We describe the clinical and biological characteristics and outcome o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c46d178fa6afbeee8d90594fbdf937a
https://doi.org/10.3109/10428194.2016.1141407
https://doi.org/10.3109/10428194.2016.1141407
Autor:
Fernando Aguirre, Andrea Candás, Vanesa Avalos Gómez, Alejandro Chaves, Aurora Feliú Torres, Mariana Bonduel, Berenice Milanesio, Carolina Pepe, Carolina Cervio, Silvia Eandi Eberle, Gabriela Sciuccati, Diego Fernandez, Lilián Díaz
Publikováno v:
Archivos argentinos de pediatría, Volume: 117, Issue: 4, Pages: 267-270, Published: 01 AUG 2019
La deficiencia de glucosa-6-fosfato deshidrogenasa es la enzimopatía eritrocitaria causada por mutaciones en el gen G6PD, cuya herencia está ligada al cromosoma X. Se analizan las características clínicas y de laboratorio de 24 individuos con def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d3cc930f6bb2c7f79ef317055f148c7
https://pubmed.ncbi.nlm.nih.gov/31339274
https://pubmed.ncbi.nlm.nih.gov/31339274
Autor:
Adrian Turjanski, Carolina Pepe, Silvia Eandi Eberle, Alejandro Chaves, Berenice Milanesio, Fernando Aguirre, Aurora Feliu-Torres, Diego Fernandez, Lucas A. Defelipe
Publikováno v:
Clinical biochemistry. 58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbeabc2fbf8fa3a3d5b5e23d695baa2a
https://pubmed.ncbi.nlm.nih.gov/26827633
https://pubmed.ncbi.nlm.nih.gov/26827633
Autor:
Raquel Mitchell, Jorge Rossi, Myriam Guitter, Angelica Fernandez-Barbieri, Patricia L. Rubio, Andrea Bernasconi, Edgardo M Baialardo, Silvia Eandi-Eberle, Maria S. Felice, E.O. Sajaroff, Cristina N. Alonso, Jorge Alberto Digiorge
Publikováno v:
Leukemia research. 71
Several conventions have been established in order to define and characterize Mixed Phenotype Acute Leukemia (MPAL). However, megakaryocytic markers have not been included in the definition of MPAL neither in the European Group for the Immunological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0b92a9f5b7ef2e1d4c7b83c83a3b8ab
https://pubmed.ncbi.nlm.nih.gov/29935384
https://pubmed.ncbi.nlm.nih.gov/29935384