Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Matteo Garibaldi"'
Autor:
Camilla MM Strano, Luca Bosco, Christian Laurini, Giacomo Sferruzza, Carla Butera, Yuri M. Falzone, Benedetta Sorrenti, Adele Ratti, Laura Tufano, Luca Leonardi, Gloria Merlonghi, Stefania Morino, Simonetta Gerevini, Ubaldo Del Carro, Matteo Garibaldi, Massimo Filippi, Stefano C Previtali
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 8, Pp 2123-2137 (2024)
Abstract Objectives Neurogenic muscle hypertrophy (NMH) is a rare condition characterized by focal muscle hypertrophy caused by chronic partial nervous injury. Given its infrequency, underlying mechanisms remain poorly understood. Inspired by two cli
Externí odkaz:
https://doaj.org/article/8d1b9752bf6e49a69cb6c940ea262b93
Autor:
Marco Fiore, Chiara Cambieri, Laura Libonati, Federica Moret, Edoardo D’Andrea, Maria Grazia Di Certo, Claudio Passananti, Francesca Gabanella, Nicoletta Corbi, Matteo Garibaldi, Cristina Chimenti, Maria Alfarano, Giampiero Ferraguti, Silvia Francati, Maurizio Inghilleri, Marco Ceccanti
Publikováno v:
Antioxidants, Vol 13, Iss 8, p 998 (2024)
Transthyretin-mediated amyloidosis (ATTR) is a systemic disease with protein precipitation in many tissues, mainly the peripheral nerve and heart. Both genetic (ATTRv, “v” for variant) and wild-type (ATTRwt) forms are known. Beyond the steric enc
Externí odkaz:
https://doaj.org/article/e8d804124ab74e64b2b966aa9b3d32f0
Autor:
Vincenzo Russo, Giovanni Antonini, Roberto Massa, Carlo Casali, Alfredo Mauriello, Anna Maria Martino, Roberto Marconi, Matteo Garibaldi, Pasquale Franciosa, Massimo Zecchin, Carlo Gaudio, Antonello D’Andrea, Stefano Strano
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 2, p 63 (2024)
Myotonic dystrophy is a hereditary disorder with systemic involvement. The Italian Neuro-Cardiology Network-“Rete delle Neurocardiologie” (INCN-RNC) is a unique collaborative experience involving neurology units combined with cardio-arrhythmology
Externí odkaz:
https://doaj.org/article/add6358ab6914d319127cc6ca2e48918
Autor:
Maria Carolina Colucci, Marica Fabiana Triolo, Simona Petrucci, Flaminia Pugnaloni, Massimiliano Corsino, Melania Evangelisti, Maria Cecilia D’Asdia, Giovanni Di Nardo, Matteo Garibaldi, Gianluca Terrin, Pasquale Parisi
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-5 (2022)
Abstract Background Hypokalemic periodic paralysis is a rare neuromuscular genetic disorder due to defect of ion channels and subsequent function impairment. It belongs to a periodic paralyses group including hyperkalemic periodic paralysis (HEKPP),
Externí odkaz:
https://doaj.org/article/9fb662ea4c8f4d1d8b6f5d738db8e262
Autor:
Marta Piras, Martina Panebianco, Matteo Garibaldi, Michela Roberto, Gioia Merlonghi, Patrizia Pellegrini, Paolo Marchetti
Publikováno v:
Current Oncology, Vol 28, Iss 3, Pp 1957-1961 (2021)
Introduction. Dermatomyositis (DM) is an idiopathic inflammatory myopathy (IIM) mainly characterized by subacute muscle weakness and skin rash sometimes associated with malignancy. Case Presentation. A 61-year-old female was admitted to our hospital
Externí odkaz:
https://doaj.org/article/d94e774ac4754c1c91b8e93a8930f3a0
Autor:
Marco Ceccanti, Chiara Cambieri, Laura Libonati, Giorgio Tartaglia, Federica Moret, Matteo Garibaldi, Maurizio Inghilleri
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundMany different trials were assessed for rehabilitation of patients with amyotrophic lateral sclerosis (ALS), with non-unique results. Beside the effects on muscle trophism, some of the encouraging results of physical training could be ascri
Externí odkaz:
https://doaj.org/article/6eeda17e9a3b4dc3a7a19526a3f0e712
Autor:
Nelida Inés Noguera, Daniela Tavian, Corrado Angelini, Francesca Cortese, Massimiliano Filosto, Matteo Garibaldi, Sara Missaglia, Ariela Smigliani, Alessandra Zaza, Elena Maria Pennisi
Publikováno v:
Biomolecules, Vol 13, Iss 3, p 452 (2023)
Neutral lipid storage disease type M (NLSD-M) is an ultra-rare, autosomal recessive disorder that causes severe skeletal and cardiac muscle damage and lipid accumulation in all body tissues. In this hereditary pathology, the defective action of the a
Externí odkaz:
https://doaj.org/article/303a9186856f47cea1076b47b9e584ee
Autor:
Chiara Cambieri, Laura Libonati, Federica Moret, Giorgio Tartaglia, Matteo Garibaldi, Cristina Chimenti, Maurizio Inghilleri, Marco Ceccanti
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2073 (2022)
Background: Transthyretin-mediated amyloidosis (ATTR) is a rare multisystemic disease involving the peripheral nervous system and heart. Autonomic and small fiber involvement is one of the hallmarks of ATTR, and many tools have been proposed to asses
Externí odkaz:
https://doaj.org/article/59ed2f8865944fe19340fc0e435ae6a2
Autor:
Matteo Garibaldi, John Rendu, Julie Brocard, Emmanuelle Lacene, Julien Fauré, Guy Brochier, Maud Beuvin, Clemence Labasse, Angeline Madelaine, Edoardo Malfatti, Jorge Alfredo Bevilacqua, Fabiana Lubieniecki, Soledad Monges, Ana Lia Taratuto, Jocelyn Laporte, Isabelle Marty, Giovanni Antonini, Norma Beatriz Romero
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-19 (2019)
Abstract Several morphological phenotypes have been associated to RYR1-recessive myopathies. We recharacterized the RYR1-recessive morphological spectrum by a large monocentric study performed on 54 muscle biopsies from a large cohort of 48 genetical
Externí odkaz:
https://doaj.org/article/c73f5437deee409b931e8b9a6c5226cb
Autor:
Celia Cordero-Sanchez, Beatrice Riva, Simone Reano, Nausicaa Clemente, Ivan Zaggia, Federico A. Ruffinatti, Alberto Potenzieri, Tracey Pirali, Salvatore Raffa, Sabina Sangaletti, Mario P. Colombo, Alessandra Bertoni, Matteo Garibaldi, Nicoletta Filigheddu, Armando A. Genazzani
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 2 (2020)
STIM and ORAI proteins play a fundamental role in calcium signaling, allowing for calcium influx through the plasma membrane upon depletion of intracellular stores, in a process known as store-operated Ca2+ entry. Point mutations that lead to gain-of
Externí odkaz:
https://doaj.org/article/611ada2e98354ec2808456437d74eab1