Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Iolanda Parente"'
Autor:
Angela Mauro, Iolanda Parente, Thailjlia Gagliardo, Anna Bonadies, Raffaele Mancusi, Vincenzo Tipo, Eduardo Ponticiello
Publikováno v:
Emergency Care Journal, Vol 17, Iss 1 (2021)
Methemoglobinemia is an alteration of the oxidative state of hemoglobin. When methemoglobin values rise above 10%, the symptoms and signs related to this condition appear, such as cyanosis, respiratory problems, fatigue and headache. Acquired methemo
Externí odkaz:
https://doaj.org/article/51bf01f8ef65400d9c464104f997bcd1
Autor:
Vincenzo Tipo, Thailjlia Gagliardo, Eduardo Ponticiello, Angela Mauro, Anna Bonadies, Iolanda Parente, Raffaele Mancusi
Publikováno v:
Emergency Care Journal, Vol 17, Iss 1 (2021)
Methemoglobinemia is an alteration of the oxidative state of hemoglobin. When methemoglobin values rise above 10%, the symptoms and signs related to this condition appear, such as cyanosis, respiratory problems, fatigue and headache. Acquired methemo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a81bfdd1b47e312da243c2b6b9fd983
https://www.pagepressjournals.org/index.php/ecj/article/view/9089
https://www.pagepressjournals.org/index.php/ecj/article/view/9089
Autor:
Jean-François Ghersi-Egea, Mathieu Santin, Christiane Charriaut-Marlangue, Mickael Tanter, Fabienne Glacial, Luigi Titomanlio, Stéphane Lehéricy, Zsolt Csaba, Charlie Demene, Pierre-Louis Leger, Pascal Dournaud, Bérard Coqueran, Stéphane Auvin, Iolanda Parente, Alice Jacquens, Isabelle Margaill, Homa Adle-Biassette, Jean-François Aubry, Pierre Gressens, Charlotte Constans, Nicolas Perrière, Tania Vitalis
Publikováno v:
Neuropathology and Applied Neurobiology
Neuropathology and Applied Neurobiology, 2021, 47 (2), pp.297-315. ⟨10.1111/nan.12665⟩
Neuropathology and Applied Neurobiology, 2021, 47 (2), pp.297-315. ⟨10.1111/nan.12665⟩
We introduce a novel approach based on agonist‐induced internalization of a neuronal G protein‐coupled receptor widely distributed in the mammalian brain, the somatostatin receptor type 2 (SST2).This approach provides an alternative and simple ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03cf08e65f5f6f615d024a87931ccdae
https://hal.science/hal-03818501
https://hal.science/hal-03818501
Autor:
Iolanda Parente, Alfonso Romano, Floriana Imperati, Marina Riccitelli, Roberto Berni Canani, Mattia Gentile, Ennio Del Giudice, Orazio Palumbo, Alessandra D'Amico, Gaetano Terrone, Massimo Carella, Daniela Melis
The 17q21.31 microdeletion syndrome is a genetic disorder characterized by intellectual disability, facial dysmorphisms and a typical behavioral phenotype. Patients are usually described as friendly and cooperative but they can also show behavioral p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecd0531fcfed61e52a8732fc58734cd1
http://hdl.handle.net/11588/477977
http://hdl.handle.net/11588/477977