Works matching AU Rodolico, C.

Results: 25

NfL as a biomarker in ATTRv amyloidosis: potential and limitations.

Published in:

Neurological Sciences, 2025, v. 46, n. 7, p. 3263, doi. 10.1007/s10072-025-08110-0

By:

Russo, Massimo;
De Luca, M.;
Gentile, L.;
D'Arma, F.;
Pugliese, A.;
Macaione, V.;
Polito, F.;
Licitri, L.;
Cafarchio, A.;
Aguennouz, M. H.;
Rodolico, C.;
Mazzeo, A.

Publication type:

Article

Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL.

Published in:

Human Mutation, 2006, v. 27, n. 6, p. 600, doi. 10.1002/humu.9426

By:

Lucchiari, S.;
Pagliarani, S.;
Salani, S.;
Filocamo, M.;
Di Rocco, M.;
Melis, D.;
Rodolico, C.;
Musumeci, O.;
Toscano, A.;
Bresolin, N.;
Comi, G.P.

Publication type:

Article

Clinical, morphological and genetic features of a cohort of late onset GSD II patients: typical and atypical presentations.

Published in:

2013

By:

Barca, E.;
Musumeci, O.;
Rodolico, C.;
Ciranni, A.;
Vita, G.;
Toscano, A.

Publication type:

Abstract

A Family With Autosomal Dominant Mutilating Neuropathy Not Linked To Either Charcot-Marie-Tooth Disease Type 2B (CMT2B) or Hereditary Sensory Neuropathy Type I (HSN I) LOCI.

Published in:

Journal of the Peripheral Nervous System, 2002, v. 7, n. 3, p. 211, doi. 10.1046/j.1529-8027.2002.02026_23.x

By:

Bellone, E;
Rodolico, C;
Toscano, A;
Di Maria, E;
Cassandrini, D;
Pizzuti, A;
Pigullo, S;
Mazzeo, A;
Macaione, V;
Girlanda, P;
Vita, G;
Ajmar, F;
Mandich, P.

Publication type:

Article

A FAMILY WITH AUTOSOMAL DOMINANT MUTILATING NEUROPATHY NOT LINKED TO EITHER 3q13-q22 OR 9q22 LOCI.

Published in:

Journal of the Peripheral Nervous System, 2000, v. 5, n. 1, p. 33, doi. 10.1046/j.1529-8027.2000.00513-3.x

By:

Bellone, E.;
Di Maria, E.;
Cassandrini, D.;
Rodolico, C.;
Mazzeo, A.;
Girlanda, P.;
Vita, G.;
Pizzuti, A.;
Toscano, A.;
Ajmar, F.;
Mandich, P.

Publication type:

Article

Myopathy as the Persistently Isolated Symptomatology of Primary Autoimmune Hypothyroidism.

Published in:

Thyroid, 1998, v. 8, n. 11, p. 1033, doi. 10.1089/thy.1998.8.1033

By:

RODOLICO, C.;
TOSCANO, A.;
BENVENGA, S.;
MAZZEO, A.;
BARTOLONE, S.;
BARTOLONE, L.;
GIRLANDA, P.;
MONICI, M.C.;
MIGLIORATO, A.;
TRIMARCHI, F.;
VITA, G.

Publication type:

Article

MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2B.

Published in:

Cell Biochemistry & Function, 2016, v. 34, n. 6, p. 414, doi. 10.1002/cbf.3202

By:

Aguennouz, M.;
Lo Giudice, C.;
Licata, N.;
Rodolico, C.;
Musumeci, O.;
Fanin, M.;
Migliorato, A.;
Ragusa, M.;
Macaione, V.;
Di Giorgio, R. M.;
Angelini, C.;
Toscano, A.

Publication type:

Article

Expanding the histopathological spectrum of <italic>CFL2</italic>‐related myopathies.

Published in:

Clinical Genetics, 2018, v. 93, n. 6, p. 1234, doi. 10.1111/cge.13240

By:

Fattori, F.;
Fiorillo, C.;
Rodolico, C.;
Tasca, G.;
Verardo, M.;
Bellacchio, E.;
Pizzi, S.;
Ciolfi, A.;
Fagiolari, G.;
Lupica, A.;
Broda, P.;
Pedemonte, M.;
Moggio, M.;
Bruno, C.;
Tartaglia, M.;
Bertini, E.;
D'Amico, A.

Publication type:

Article

Chinese red rice depletes muscle coenzyme Q10 and maintains muscle damage after discontinuation of statin treatment.

Published in:

2006

By:

Vercelli L;
Mongini T;
Olivero N;
Rodolico C;
Musumeci O;
Palmucci L

Publication type:

Journal Article

MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients.

Published in:

2016

By:

Fiorillo, C.;
Astrea, G.;
Savarese, M.;
Cassandrini, D.;
Brisca, G.;
Trucco, F.;
Pedemonte, M.;
Trovato, R.;
Ruggiero, L.;
Vercelli, L.;
D'Amico, A.;
Tasca, G.;
Pane, M.;
Fanin, M.;
Bello, L.;
Broda, P.;
Musumeci, O.;
Rodolico, C.;
Messina, S.;
Vita, G. L.

Publication type:

journal article

Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.

Published in:

Journal of Inherited Metabolic Disease, 1999, v. 22, n. 6, p. 762, doi. 10.1023/A:1005572906807

By:

Hadjigeorgiou, G.;
Comi, G.;
Bordoni, A.;
Shen, J.;
Chen, Y.-T.;
Salani, S.;
Toscano, A.;
Fortunato, F.;
Lucchiari, S.;
Bresolin, N.;
Rodolico, C.;
Piscaglia, M.;
Franceschina, L.;
Papadimitriou, A.;
Scarlato, G.

Publication type:

Article

Value of insoluble PABPN1 accumulation in the diagnosis of oculopharyngeal muscular dystrophy.

Published in:

European Journal of Neurology, 2020, v. 27, n. 4, p. 709, doi. 10.1111/ene.14131

By:

Galimberti, V.;
Tironi, R.;
Lerario, A.;
Scali, M.;
Del Bo, R.;
Rodolico, C.;
Brizzi, T.;
Gibertini, S.;
Maggi, L.;
Mora, M.;
Toscano, A.;
Comi, G. P.;
Sciacco, M.;
Moggio, M.;
Peverelli, L.

Publication type:

Article

Italian recommendations for Lambert-Eaton myasthenic syndrome (LEMS) management.

Published in:

Neurological Sciences, 2014, v. 35, n. 4, p. 515, doi. 10.1007/s10072-014-1637-4

By:

Evoli, A.;
Liguori, R.;
Romani, A.;
Mantegazza, R.;
Muzio, A.;
Giometto, B.;
Pegoraro, E.;
Rodolico, C.;
Vigliani, M.

Publication type:

Article

ANT1 is reduced in sporadic inclusion body myositis.

Published in:

Neurological Sciences, 2013, v. 34, n. 2, p. 217, doi. 10.1007/s10072-012-0976-2

By:

Barca, E.;
Aguennouz, M.;
Mazzeo, A.;
Messina, S.;
Toscano, A.;
Vita, G.;
Portaro, S.;
Parisi, D.;
Rodolico, C.

Publication type:

Article

Wound botulism in drug users: a still underestimated diagnosis.

Published in:

Neurological Sciences, 2010, v. 31, n. 6, p. 825, doi. 10.1007/s10072-010-0350-1

By:

Rodolico, C.;
Barca, E.;
Fenicia, L.;
Anniballi, F.;
Sinardi, A. U.;
Girlanda, P.

Publication type:

Article

Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci.

Published in:

Neurological Sciences, 2005, v. 26, n. 5, p. 303, doi. 10.1007/s10072-005-0502-x

By:

Rodolico, C.;
Toscano, A.;
Patitucci, A.;
Muglia, M.;
Gaeta, M.;
D’Arrigo, G.;
Migliorato, A.;
Messina, S.;
Quattrone, A.;
Messina, C.;
Vita, G.

Publication type:

Article

Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families.

Published in:

Acta Neurologica Scandinavica, 2008, v. 118, n. 5, p. 328, doi. 10.1111/j.1600-0404.2008.01021.x

By:

Mazzeo, A.;
Muglia, M.;
Rodolico, C.;
Toscano, A.;
Patitucci, A.;
Quattrone, A.;
Messina, C.;
Vita, G.

Publication type:

Article

Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies.

Published in:

Acta Neurologica Scandinavica, 2008, v. 117, n. 6, p. 393, doi. 10.1111/j.1600-0404.2007.00957.x

By:

Macaione, V.;
Aguennouz, M.;
Mazzeo, A.;
De Pasquale, M. G.;
Russo, M.;
Toscano, A.;
De Luca, G.;
Di Giorgio, R. M.;
Vita, G.;
Rodolico, C.

Publication type:

Article

RAGE-NF- κB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophy.

Published in:

Acta Neurologica Scandinavica, 2007, v. 115, n. 2, p. 115, doi. 10.1111/j.1600-0404.2006.00724.x

By:

Macaione, V.;
Aguennouz, M.;
Rodolico, C.;
Mazzeo, A.;
Patti, A.;
Cannistraci, E.;
Colantone, L.;
di Giorgio, R. M.;
de Luca, G.;
Vita, G.

Publication type:

Article

Specific matrix metalloproteinase expression in focal myositis: an immunopathological study.

Published in:

Acta Neurologica Scandinavica, 2005, v. 112, n. 3, p. 173, doi. 10.1111/j.1600-0404.2005.00457.x

By:

Rodolico, C.;
Mazzeo, A.;
Toscano, A.;
Messina, S.;
Aguennouz, M.;
Gaeta, M.;
Messina, C.;
Vita, G.

Publication type:

Article

Long-Term Follow-Up in Infantile-Onset Lambert-Eaton Myasthenic Syndrome.

Published in:

2014

By:

Portaro, S.;
Parisi, D.;
Polizzi, A.;
Ruggieri, M.;
Andreetta, F.;
Bernasconi, P.;
Toscano, A.;
Rodolico, C.

Publication type:

Case Study

Endocrine evaluation for muscle pain.

Published in:

2001

By:

Benvenga, S;
Toscano, A;
Rodolico, C;
Vita, G;
Trimarchi, F

Publication type:

journal article

Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatment.

Published in:

Journal of Neurology, 2015, v. 262, n. 4, p. 968, doi. 10.1007/s00415-015-7664-0

By:

Montagnese, Federica;
Barca, E.;
Musumeci, O.;
Mondello, S.;
Migliorato, A.;
Ciranni, A.;
Rodolico, C.;
Filippi, P.;
Danesino, C.;
Toscano, A.

Publication type:

Article

Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene.

Published in:

Human Mutation, 2000, v. 15, n. 3, p. 299, doi. 10.1002/(SICI)1098-1004(200003)15:3<299::AID-HUMU24>3.0.CO;2-Z

By:

Muglia, M.;
Toscano, A.;
Gabriele, A.L.;
Magariello, A.;
Patitucci, A.;
Conforti, F.L.;
Mazzei, R.;
Rodolico, C.;
Gambardella, A.;
Quattrone, A.

Publication type:

Article

Hypnic Headache Responsive to Low-Dose Topiramate: A Case Report.

Published in:

2008

By:

Autunno M;
Messina C;
Blandino A;
Rodolico C

Publication type:

Journal Article