Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Anita Sofia Bellotti"'
Autor:
Benedetta Chiodini, Anita Sofia Bellotti, William Morello, Chiara Bulgaro, Ilaria Farella, Mario Giordano, Giovanni Montini, Khalid Ismaili, Karl Martin Wissing
BACKGROUND: Viral upper respiratory tract infections trigger nephrotic syndrome relapses. Few data exist on the impact of the SARS-CoV-2 pandemic on the risk of relapse in children with idiopathic nephrotic syndrome (INS). METHODS: In a Belgian and I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4980b16efd380d38c743bbd0dba71677
https://biblio.vub.ac.be/vubir/relapse-rate-in-children-with-nephrotic-syndrome-during-the-sarscov2-pandemic(c2611499-980e-493e-8d41-8a0622b372a3).html
https://biblio.vub.ac.be/vubir/relapse-rate-in-children-with-nephrotic-syndrome-during-the-sarscov2-pandemic(c2611499-980e-493e-8d41-8a0622b372a3).html
Autor:
Giacomo P. Comi, Stefania Corti, Luca Andreoli, Dario Ronchi, Anita Sofia Bellotti, Nereo Bresolin
Publikováno v:
Molecular Neurobiology. 57:1259-1280
Glycogen storage disease type II (GSDII, Pompe disease) is a rare metabolic disorder caused by a deficiency of acid alpha-glucosidase (GAA), an enzyme localized within lysosomes that is solely responsible for glycogen degradation in this compartment.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::908fb0c253d8146706d4475d3f4736c5
https://doi.org/10.1007/s12035-019-01820-5
https://doi.org/10.1007/s12035-019-01820-5
