Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Laura, Palmucci"'
Autor:
Quaglino, Laura Palmucci
Publikováno v:
Arte Lombarda, 2004 Jan 01141 (2), 63-68.
Externí odkaz:
https://www.jstor.org/stable/43132540
Autor:
Aime, Laura Palmucci - Laura
Publikováno v:
Studi Piemontesi; giu2021, Vol. 50 Issue 1, p47-75, 29p
Autor:
Sabina Tangerini, Lisa Di Mascolo, Franco Locatelli, Laura Palmucci, Alessia Montanari, Marilena Bertini, Mattia Viano, Chiara Schiavo
Publikováno v:
J. of Health Science. 6
Autor:
Gabriele Siciliano, Ebe Pastorello, Corrado Angelini, P. Cudia, C. Borsato, Laura Palmucci, Enzo Ricci, Rita Di Leo, Francesca Greco, G. Fabbri, Leopoldo Ricciardi, M. Servida, Claudia Manzoli, Lucio Santoro, Giuliana Galluzzi, Rossella Tupler, Leda Volpi, Giuliano Tomelleri, Costanza Lamperti, Liliana Vercelli, Roberto D'Amico, Roberto Frusciante, Michelangelo Cao, Carmelo Rodolico, Maurizio Moggio, Emanuela Bonifazi, Chiara Fiorillo
Publikováno v:
Muscle & Nerve. 42:213-217
To define numerically the clinical severity of facioscapulohumeral muscular dystrophy (FSHD), we developed a protocol that quantifies muscle weakness by combining the functional evaluation of six muscle groups affected in this disease. To validate re
Autor:
Tiziana Mongini, Giuliano Tomelleri, Paola Tonin, Laura Palmucci, Roberto L'erario, Matteo Marini, Nicolo' Rizzuto, Gaetano Vattemi
Publikováno v:
Brain. 129:2085-2092
We describe four patients, from four different families, affected by a mild myopathy or asymptomatic elevated serum creatine kinase levels, in whom toluidine blue-stained semithin sections of muscle specimens revealed inclusions of different size and
Autor:
Tiziana Mongini, Marco Piccinini, Laura Palmucci, Maria Teresa Rinaudo, Barbara Buccinnà, Sabrina Leombruni, Giovanna Vaula, Alfredo Brusco, Maria Teresa Giordana, Cristina Ramondetti
Publikováno v:
Scopus-Elsevier
Brain Pathol
Brain Pathol
Adult-onset dominant leukodystrophies are a heterogeneous group of rare disorders, whose etiology, pathogenesis and molecular background are still unknown. We report the neuropathological and biochemical investigations of the brains and their myelin
Akademický článek
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Autor:
Tiziana Mongini, Joseph M. Devaney, Elena Pegoraro, Richard F. Mayer, Christoph Fahlke, Michael J. Giuliani, Aisling M. Ryan, Fen Fen Wu, Maike Warnstedt, Kevin J. Felice, Laura Palmucci, Michael A. Marino, Maria Jose Escriva, Reinhardt Rüdel, Eric P. Hoffman, Zeljka Korade-Mirnics, Barbara Poser, Audrey S. Yee
Publikováno v:
Brain. 125:2392-2407
Myotonia is a condition characterized by impaired relaxation of muscle following sudden forceful contraction. We systematically screened all 23 exons of the CLCN1 gene in 88 unrelated patients with myotonia and identified mutations in 14 patients. Si
Autor:
Olivia Musumeci, Nadia Olivero, Carmelo Rodolico, Liliana Vercelli, Tiziana Mongini, Laura Palmucci
Publikováno v:
Journal of the American Geriatrics Society. 54:718-720