Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Pietro Palumbo"'
Autor:
Alberto Visioli, Nadia Trivieri, Gandino Mencarelli, Fabrizio Giani, Massimiliano Copetti, Orazio Palumbo, Riccardo Pracella, Maria Grazia Cariglia, Chiara Barile, Luigi Mischitelli, Amata Amy Soriano, Pietro Palumbo, Federico Legnani, Francesco DiMeco, Leonardo Gorgoglione, Graziano Pesole, Angelo L. Vescovi, Elena Binda
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 42, Iss 1, Pp 1-17 (2023)
Abstract Background Glioblastoma (GBM) is the most malignant among gliomas with an inevitable lethal outcome. The elucidation of the physiology and regulation of this tumor is mandatory to unravel novel target and effective therapeutics. Emerging con
Externí odkaz:
https://doaj.org/article/1e15644cd66b4514a5bd641eb828b5a6
Autor:
Giorgia Dinoi, Elena Conte, Orazio Palumbo, Mario Benvenuto, Maria Antonietta Coppola, Pietro Palumbo, Patrizia Lastella, Brigida Boccanegra, Ester Di Muro, Marco Castori, Massimo Carella, Vittorio Sciruicchio, Marina de Tommaso, Antonella Liantonio, Annamaria De Luca, Angela La Neve, Paola Imbrici
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1698 (2024)
Loss-, gain-of-function and mixed variants in SCN1A (Nav1.1 voltage-gated sodium channel) have been associated with a spectrum of neurologic disorders with different severity and drug-responsiveness. Most SCN1A variants are heterozygous changes occur
Externí odkaz:
https://doaj.org/article/1301cdd3bed04a10ad83ef8e40aba0bf
Autor:
Laura Pignata, Francesco Cecere, Fabio Acquaviva, Emilia D’Angelo, Daniela Cioffi, Valeria Pellino, Orazio Palumbo, Pietro Palumbo, Massimo Carella, Angela Sparago, Daniele De Brasi, Flavia Cerrato, Andrea Riccio
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
Imprinting disorders are congenital diseases caused by dysregulation of genomic imprinting, affecting growth, neurocognitive development, metabolism and cancer predisposition. Overlapping clinical features are often observed among this group of disea
Externí odkaz:
https://doaj.org/article/e9967b43ef824f1aad5e0516a7eb96e9
Autor:
Giuseppe d'Orsi, Andrea Farolfi, Lorenzo Muccioli, Orazio Palumbo, Pietro Palumbo, Sergio Modoni, Vincenzo Allegri, Valentina Garibotto, Maria Teresa Di Claudio, Ester Di Muro, Mario Benvenuto, Francesca Bisulli, Massimo Carella
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
PurposeTo evaluate the electro-clinical features in association with laboratory and instrumental correlates of neurodegeneration to detect the progression of Lafora disease (LD).MethodsWe investigated the electro-clinical longitudinal data and CSF A
Externí odkaz:
https://doaj.org/article/b8d93cea68bb4ca2abe0188201e25088
Autor:
Angela Maggio, Sandra Mastroianno, Giuseppe Di Stolfo, Stefano Castellana, Pietro Palumbo, Maria Pia Leone, Anita Spirito, Domenico Rosario Potenza, Saverio Ladogana, Marco Castori, Massimo Carella, Massimo Villella, Mauro Pellegrino Salvatori
Publikováno v:
Cardiogenetics, Vol 12, Iss 1, Pp 80-88 (2022)
In thelast few decades, the roles of cardio-oncology and cardiovascular geneticsgained more and more attention in research and daily clinical practice, shaping a new clinical approach and management of patients affected by cancer and cardiovascular d
Externí odkaz:
https://doaj.org/article/8ecb0c9a77b748b0834bf478c6d69dd4
Autor:
Marcello Presutti, Remo Goderecci, Pietro Palumbo, Alessio Giannetti, Manuel Giovanni Mazzoleni, Filippo Maria Nicola Randelli, Massimo Angelozzi, Vittorio Calvisi, Andrea Fidanza
Publikováno v:
Journal of Orthopaedics and Traumatology, Vol 22, Iss 1, Pp 1-14 (2021)
Abstract Background High tibial osteotomy (HTO) provides reliable and good long-term results, if performed with correct indications, but different techniques and types of fixation have been described. The purpose of this study is to present a novel m
Externí odkaz:
https://doaj.org/article/e964dc9af9834ee0bfcd7332c5a80994
Autor:
Maria Pia Leone, Pietro Palumbo, Orazio Palumbo, Ester Di Muro, Massimiliano Chetta, Nicola Laforgia, Nicoletta Resta, Alessandro Stella, Stefano Castellana, Tommaso Mazza, Marco Castori, Massimo Carella, Nenad Bukvic
Publikováno v:
Italian Journal of Pediatrics, Vol 46, Iss 1, Pp 1-9 (2020)
Abstract Background Schinzel-Giedion syndrome (SGS) is a multiple malformation syndrome mainly characterized by severe intellectual disability, distinctive facial features, and multiple congenital anomalies, including skeletal abnormalities, genitour
Externí odkaz:
https://doaj.org/article/1c022617883045e4a95bf51de2fc4354
Autor:
Maria Pia Leone, Pietro Palumbo, Johan Saenen, Sandra Mastroianno, Stefano Castellana, Cesare Amico, Tommaso Mazza, Domenico Rosario Potenza, Antonio Petracca, Marco Castori, Massimo Carella, Giuseppe Di Stolfo
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Background: Arrhythmogenic cardiomyopathy (ACM) is a genetic disorder with an estimated prevalence between 1:2,000 and 1:5,000 and is characterized by the fibrofatty replacement of cardiomyocytes that predisposes to malignant arrhythmias, heart failu
Externí odkaz:
https://doaj.org/article/4f23d0f45da64fde90751a8808c156d6
Autor:
Valentina Agnusdei, Sonia Minuzzo, Marica Pinazza, Alessandra Gasparini, Laura Pezzè, Adriana Agnese Amaro, Lorenza Pasqualini, Paola Del Bianco, Martina Tognon, Chiara Frasson, Pietro Palumbo, Yari Ciribilli, Ulrich Pfeffer, Massimo Carella, Alberto Amadori, Stefano Indraccolo
Publikováno v:
Haematologica, Vol 105, Iss 5 (2020)
Despite substantial progress in treatment of T-cell acute lymphoblastic leukemia (T-ALL), mortality remains relatively high, mainly due to primary or acquired resistance to chemotherapy. Further improvements in survival demand better understanding of
Externí odkaz:
https://doaj.org/article/9da59cf5276c4fad8340659c500323c4
Autor:
Giuseppe Di Stolfo, Maria Accadia, Sandra Mastroianno, Maria P. Leone, Orazio Palumbo, Pietro Palumbo, Domenico Potenza, Pasquale Maccarone, Michele Sacco, Aldo Russo, Massimo Carella
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Abstract Background The deletion of the distal 7q region is a rare chromosomal syndrome characterized by wide phenotypic manifestations including growth and psychomotor delay, facial dysmorphisms, and genitourinary malformations. Methods We describe
Externí odkaz:
https://doaj.org/article/66df66181b6a4256886e1cfab5ed1943