Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Francesca Elli"'
Autor:
Elisa R. Zanier, Francesca Pischiutta, Eliana Rulli, Alessia Vargiolu, Francesca Elli, Paolo Gritti, Giuseppe Gaipa, Daniela Belotti, Gianpaolo Basso, Tommaso Zoerle, Nino Stocchetti, Giuseppe Citerio, on behalf of the MATRIx Study group
Publikováno v:
Intensive Care Medicine Experimental, Vol 11, Iss 1, Pp 1-11 (2023)
Abstract Background Traumatic brain injury (TBI) is a significant cause of death and disability, with no effective neuroprotective drugs currently available for its treatment. Mesenchymal stromal cell (MSC)-based therapy shows promise as MSCs release
Externí odkaz:
https://doaj.org/article/7ba941349f5048babfbfcfb645974657
Autor:
Walter Vena, Valentina Morelli, Maria Carrabba, Francesca Elli, Giovanna Fabio, Ilaria Muller, Camilla Lucca, Maria Antonia Maffini, Andrea Gerardo Lania, Giovanna Mantovani, Maura Arosio
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Primary bilateral macronodular adrenal hyperplasia (PBMAH) represents an uncommon cause of endogenous hypercortisolism. Since the first description in 2003 in a French cohort, many papers have been published describing families as well as isolated in
Externí odkaz:
https://doaj.org/article/5e9708645e1841b280baf47e66b1547f
Autor:
Giuseppe Citerio, Mauro Oddo, Fabio Taccone, Francesca Elli, Alessia Vargiolu, Stefania Galimberti, Paola Rebora, R Badenes, P Bouzat, A Caricato, RM Chesnut, C Hemphill, F Rasulo, S Schwab, JI Suarez, K Sunde, Aaron Blandino, Letterio Malgeri, Eleonora Rossi, Francesca Graziano
Publikováno v:
BMJ Open, Vol 11, Iss 5 (2021)
Introduction The pupillary examination is an important part of the neurological assessment, especially in the setting of acutely brain-injured patients, and pupillary abnormalities are associated with poor outcomes. Currently, the pupillary examinati
Externí odkaz:
https://doaj.org/article/8cec9310da51458286b45aa68b727761
Autor:
Mario Cozzolino, Francesco Cosa, Paola Ciceri, Francesca Elli, Flavia Ricca, Laura Cappelletti, Antonio Bellasi, Daniele Cusi
Publikováno v:
European Medical Journal Nephrology, Vol 1, Iss 1, Pp 46-51 (2013)
Vascular calcification involves passive degeneration and an active process of arterial mineralisation, resembling osteogenesis. In chronic kidney disease, several proteins that physiologically control bone mineralisation, are also involved in the mol
Externí odkaz:
https://doaj.org/article/fc4e1f6ea09e4965828230466bdb0e34
Publikováno v:
Giornale di Clinica Nefrologia e Dialisi, Vol 27, Iss 2 (2015)
Abstract non disponibile
Externí odkaz:
https://doaj.org/article/c37c0326eba64002bde1a91a042e3791
Autor:
Giulia Rodari, Roberta Villa, Matteo Porro, Silvana Gangi, Maria Iascone, Francesca Elli, Federico Giacchetti, Eriselda Profka, Valentina Collini, Alberta Dall’Antonia, Maura Arosio, Giovanna Mantovani, Maria Francesca Bedeschi, Claudia Giavoli
Publikováno v:
European Journal of Human Genetics. 31:195-201
Protein arginine methyltransferase 7 (PRMT7) pathogenetic variants have been associated with the human disorder of Short Stature, Brachydactyly, Intellectual Developmental Disability and Seizures syndrome (SBIDDS). Only 15 cases have been described i
Autor:
Geert Meyfroidt, Giorgia Carra, Bart Depreitere, Marine Flechet, Lukas Huber, Fabian Güiza, Francesca Elli, Verena Rass, Bogdan Ianosi, Giuseppe Citerio, Raimund Helbok
Publikováno v:
Neurocritical Care. 34:722-730
Background: In patients with aneurysmal subarachnoid hemorrhage (aSAH) the burden of intracranial pressure (ICP) and its contribution to outcomes remains unclear. In this multicenter study, the independent association between intensity and duration,
Autor:
Luisa De Sanctis, Francesca Elli, Guiomar Perez de Nanclares, Agnès Linglart, Susanne Thiele, Patrick Hanna, Giovanna Mantovani, Arrate Pereda, Bruno Francou, Diana-Alexandra Ertl, Anya Rothenbuhler
Publikováno v:
European Journal of Endocrinology. 184:311-320
Objective Pseudohypoparathyroidism and related disorders belong to a group of heterogeneous rare diseases that share an impaired signaling downstream of Gsα-protein-coupled receptors. Affected patients may present with various combination of symptom
Autor:
Francesca Elli, Giovanna Mantovani
Publikováno v:
Endocrine
Pseudohypoparathyroidism (PHP), the first known post-receptorial hormone resistance, derives from a partial deficiency of the α subunit of the stimulatory G protein (Gsα), a key component of the PTH/PTHrP signaling pathway. Since its first descript
Autor:
Giovanna Mantovani, Francesca Elli, Claudio Marcocci, Simona Borsari, Alessandro Brancatella, Filomena Cetani
Publikováno v:
Endocrine. 67:466-472
Pseudohypoparathyroidism (PHP), characterized by multihormone resistance and Albright’s hereditary osteodystrophy (AHO), is caused by GNAS mutations. Whole or partial gene deletions are rare. All disorders due to inactivating mutations of the GNAS