Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mafalda Caputo"'
Autor:
Flavia Antonucci, Serena Marotta, Maria Celentano, Mariangela Pedata, Cira Riccardi, Cristina Luise, Angela Carobene, Simona Maria Muggianu, Assunta Viola, Mafalda Caputo, Stefania Leone, Ilaria Migliaccio, Barbara Pocali, Mirella Alberti, Claudio Falco, Mario Toriello, Felicetto Ferrara, Alessandra Picardi
Publikováno v:
Frontiers in Hematology, Vol 3 (2024)
To date, the effect of blinatumomab and donor lymphocyte infusion association as a salvage treatment for acute lymphoblastic leukemia (ALL) relapse after allogeneic transplant procedure is still unknown. Here, we report a case report of a patient wit
Externí odkaz:
https://doaj.org/article/696d4a34f3cc49e0827dfbf48df98890
Autor:
Gabriella Ferretti, Antonella Angiolillo, Rosarita Nasso, Carmela Matrone, Alfonso Di Costanzo, Pierluigi Reveglia, Gaetano Corso, Carmela Paolillo, Mafalda Caputo, Armando De Carlo
Publikováno v:
Metabolomics
Background Alzheimer's disease (AD) is one of the most common causes of dementia in old people. Neuronal deficits such as loss of memory, language and problem-solving are severely compromised in affected patients. The molecular features of AD are Aβ
Autor:
G. Cardiero, Carola Giacobbe, Ornella Guardamagna, M.D. Di Taranto, Mafalda Caputo, Monica Gelzo, Giuliana Fortunato, Daniela De Palma, Gaetano Corso
Publikováno v:
Atherosclerosis. 331:e50-e51
Autor:
Paola Iacotucci, Vincenzo Carnovale, Gustavo Cernera, Gaetano Corso, Monica Gelzo, Mafalda Caputo, Marika Comegna, Giuseppe Castaldo
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 20(1)
Background Cystic fibrosis (CF) patients have reduced intestinal absorption of sterols and, despite enhanced endogenous synthesis, low plasma cholesterol. Lumacaftor/ivacaftor CFTR protein modulator therapy is used to improve the clinical outcome of
Autor:
Mafalda Caputo, Maria Donata Di Taranto, Rocco Capuano, Gaetano Corso, Monica Gelzo, Alessandra D'Amico, Carola Giacobbe, Alvino Bisecco, Mario Cirillo, Gioacchino Tedeschi, Giuliana Fortunato
Cerebrotendinous Xanthomatosis (CTX) is an autosomal recessive defect of the alternative pathway of bile acid biosynthesis, due to the deficiency of mitochondrial cytochrome P450 sterol 27-hydroxylase enzyme encoded by CYP27A1. The deficit of sterol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5610e0f38650189c4d66ffa74d84a13
http://hdl.handle.net/11591/421348
http://hdl.handle.net/11591/421348
Autor:
Raffaella Tortora, Wanda Utech, F. Lampasi, A. Lanza, G. Cordone, Luigi Addario, M.T. Tartaglione, Mafalda Caputo, Giuseppina Marino Marsilia, Emanuela Assentato, Massimo De Luca, F.P. Picciotto, Giovan Giuseppe Di Costanzo
Publikováno v:
Gastroenterology. 148:S-1030