Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Fainboin, A."'
Autor:
Liern, Miguel, Collazo, Anabella, Valencia, Maylin, Fainboin, Alejandro, Isse, Lorena, Costales-Collaguazo, Cristian, Ochoa, Federico, Vallejo, Graciela, Zotta, Elsa
Publikováno v:
In NEFROLOGIA (English Edition) March-April 2019 39(2):177-183
Autor:
Liern, Miguel, Collazo, Anabella, Valencia, Maylin, Fainboin, Alejandro, Isse, Lorena, Costales-Collaguazo, Cristian, Ochoa, Federico, Vallejo, Graciela, Zotta, Elsa
Publikováno v:
In NEFROLOGÍA March-April 2019 39(2):177-183
Autor:
Miguel Liern, Anabella Collazo, Maylin Valencia, Alejandro Fainboin, Lorena Isse, Cristian Costales-Collaguazo, Federico Ochoa, Graciela Vallejo, Elsa Zotta
Publikováno v:
Nefrología, Vol 39, Iss 2, Pp 177-183 (2019)
Resumen: Introducción: La enfermedad de Fabry (EF) es un trastorno hereditario causado por una deficiencia de la actividad de la enzima α-galactosidasa A, cuya transmisión está relacionada con el cromosoma X. Objetivos: Los objetivos del estudio
Externí odkaz:
https://doaj.org/article/5448e61497ce4734a4983d8344208645
Autor:
Miguel Liern, Anabella Collazo, Maylin Valencia, Alejandro Fainboin, Lorena Isse, Cristian Costales-Collaguazo, Federico Ochoa, Graciela Vallejo, Elsa Zotta
Publikováno v:
Nefrología (English Edition), Vol 39, Iss 2, Pp 177-183 (2019)
Introduction: Fabry disease (FD) is a hereditary disorder caused by a deficiency of α-galactosidase A enzyme activity. The transmission of the disorder is linked to the X chromosome. Objectives: The objectives of the study were: 1. To quantify the p
Externí odkaz:
https://doaj.org/article/c72f903a90ad41f39ad228d0f5a3a321
Autor:
Graciela Vallejo, Maylin Valencia, Cristian Costales-Collaguazo, Anabella Collazo, Alejandro Fainboin, Federico Ochoa, Lorena Isse, Miguel Liern, Elsa Zotta
Publikováno v:
Nefrología, Vol 39, Iss 2, Pp 177-183 (2019)
Resumen: Introducción: La enfermedad de Fabry (EF) es un trastorno hereditario causado por una deficiencia de la actividad de la enzima α-galactosidasa A, cuya transmisión está relacionada con el cromosoma X. Objetivos: Los objetivos del estudio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ca3f5c5e9147f3baa0b03568122319f
https://doi.org/10.1016/j.nefro.2018.05.009
https://doi.org/10.1016/j.nefro.2018.05.009
Autor:
Anabella Collazo, Graciela Vallejo, Elsa Zotta, Maylin Valencia, Alejandro Fainboin, Federico Ochoa, Miguel Liern, Cristian Costales-Collaguazo, Lorena Isse
Publikováno v:
Nefrología (English Edition), Vol 39, Iss 2, Pp 177-183 (2019)
Introduction: Fabry disease (FD) is a hereditary disorder caused by a deficiency of α-galactosidase A enzyme activity. The transmission of the disorder is linked to the X chromosome. Objectives: The objectives of the study were: 1. To quantify the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::669718beca33a0626bf897298a79a15b
https://doi.org/10.1016/j.nefroe.2019.03.001
https://doi.org/10.1016/j.nefroe.2019.03.001
Autor:
Miguel, Liern, Anabella, Collazo, Maylin, Valencia, Alejandro, Fainboin, Lorena, Isse, Cristian, Costales-Collaguazo, Federico, Ochoa, Graciela, Vallejo, Elsa, Zotta
Publikováno v:
Nefrologia. 39(2)
Fabry disease (FD) is a hereditary disorder caused by a deficiency of α-galactosidase A enzyme activity. The transmission of the disorder is linked to the X chromosome.The objectives of the study were: 1. To quantify the presence of podocytes in pae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a496404db0cf3b31bb34801dc70468f2
https://pubmed.ncbi.nlm.nih.gov/30139698
https://pubmed.ncbi.nlm.nih.gov/30139698
Autor:
Mojsiejczuk, Laura Noelia, Torres, Carolina, Fainboin, Hugo Alberto, Galdame, Omar Andres, Campos, Rodolfo Hector, Flichman, Diego Martin
Publikováno v:
In Infection, Genetics and Evolution August 2015 34:122-125
Autor:
Diego Martin Flichman, Rodolfo Hector Campos, Laura Noelia Mojsiejczuk, Omar Galdame, Hugo Alberto Fainboin, Carolina Torres
Publikováno v:
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 34
Hepatitis B virus (HBV) is classified into eight main genotypes (A–H) and several subgenotypes. Here, three new genotype F complete genome sequences isolated from patients from Buenos Aires city are reported. The new sequences form a separate monop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31184402ac4100658e6346672a518b0a
https://pubmed.ncbi.nlm.nih.gov/26073681
https://pubmed.ncbi.nlm.nih.gov/26073681
Autor:
A. Fainboin, G. Cabrera, H. Amartino, Adrián Fernández, N. Antongiovani, R. Valdez, R. Heguilen, J. Politei
Publikováno v:
Heart, Lung and Circulation. 23:e7
Familial long QT syndrome (LQTS) is the most common primary arrhythmogenic disorder. The clinical diagnosis of LQTS can be difficult, and genotype plays a vital role in early disease identification.Wesought toassess factors that impacton communicatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dd2764bf84055010127db34d2a2958c
https://doi.org/10.1016/j.hlc.2014.07.018
https://doi.org/10.1016/j.hlc.2014.07.018