C Rodolico

Summary

Affiliation: University of Messina
Country: Italy

Publications

  1. pmc The empowerment of translational research: lessons from laminopathies
    Sara Benedetti
    National Research Council of Italy, Institute of Molecular Genetics, IGM CNR, Unit of Bologna, Via Di Barbiano 1 10, 40136, Bologna, Italy
    Orphanet J Rare Dis 7:37. 2012
  2. doi request reprint Wound botulism in drug users: a still underestimated diagnosis
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, AOU G Martino, University of Messina, Messina, Italy
    Neurol Sci 31:825-7. 2010
  3. ncbi request reprint Amyloid myopathy presenting with rhabdomyolysis: evidence of complement activation
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
    Neuromuscul Disord 16:514-7. 2006
  4. ncbi request reprint Juvenile limb-girdle myasthenia gravis
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Italy
    Neuropediatrics 36:353-6. 2005
  5. ncbi request reprint Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, A O U G Martino, Via C Valeria, I 98125, Italy
    Neurol Sci 26:303-9. 2005
  6. ncbi request reprint Specific matrix metalloproteinase expression in focal myositis: an immunopathological study
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
    Acta Neurol Scand 112:173-7. 2005
  7. ncbi request reprint Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Policlinico Universitario, Via C Valeria 98125, Messina, Italy
    Neuromuscul Disord 12:964-9. 2002
  8. doi request reprint Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families
    A Mazzeo
    Department of Neurosciences, Psychiatry and Anaesthesiology University of Messina, Messina, Italy
    Acta Neurol Scand 118:328-32. 2008
  9. ncbi request reprint Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies
    V Macaione
    Department of Biochemical, Physiological and Nutritional Sciences, University of Messina, Messina, Italy
    Acta Neurol Scand 117:393-8. 2008
  10. doi request reprint ANT1 is reduced in sporadic inclusion body myositis
    E Barca
    Department of Neurosciences, Psychiatry and Anesthesiology, AOU G Martino, Messina, Italy
    Neurol Sci 34:217-24. 2013

Collaborators

Detail Information

Publications20

  1. pmc The empowerment of translational research: lessons from laminopathies
    Sara Benedetti
    National Research Council of Italy, Institute of Molecular Genetics, IGM CNR, Unit of Bologna, Via Di Barbiano 1 10, 40136, Bologna, Italy
    Orphanet J Rare Dis 7:37. 2012
    ....
  2. doi request reprint Wound botulism in drug users: a still underestimated diagnosis
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, AOU G Martino, University of Messina, Messina, Italy
    Neurol Sci 31:825-7. 2010
    ..Alerting clinicians to botulism is crucial for a rapid diagnosis and appropriate treatment and thus decreasing mortality and complications...
  3. ncbi request reprint Amyloid myopathy presenting with rhabdomyolysis: evidence of complement activation
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
    Neuromuscul Disord 16:514-7. 2006
    ..The detection of complement complex C5b9 suggests that complement cascade is implicated in the muscular damage of amyloid myopathy...
  4. ncbi request reprint Juvenile limb-girdle myasthenia gravis
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Italy
    Neuropediatrics 36:353-6. 2005
    ..Diagnosis of limb-girdle myasthenia requires a strong index of suspicion also in childhood. We suggest that this form be suspected in children with unclassifiable myopathy, mostly affecting deltoid muscles and lower extremities...
  5. ncbi request reprint Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, A O U G Martino, Via C Valeria, I 98125, Italy
    Neurol Sci 26:303-9. 2005
    ..1, 2p13, 19p13. The study suggests that quadriceps sparing is a characteristic feature also of AD-IBM. This finding could represent a muscle-image hallmark helpful in diagnosis of autosomal dominant muscular disorders...
  6. ncbi request reprint Specific matrix metalloproteinase expression in focal myositis: an immunopathological study
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
    Acta Neurol Scand 112:173-7. 2005
    ..The aim of our study was to investigate immunoexpression of matrix metalloproteinases MMP2, MMP7 and MMP9 in muscle specimens from patients with focal myositis (FM) vs polymyositis (PM) and dermatomyositis...
  7. ncbi request reprint Limb-girdle myasthenia: clinical, electrophysiological and morphological features in familial and autoimmune cases
    C Rodolico
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Policlinico Universitario, Via C Valeria 98125, Messina, Italy
    Neuromuscul Disord 12:964-9. 2002
    ..Our findings reinforce the opportunity to suspect limb-girdle myasthenia in unclassifiable proximal myopathies and to differentiate familial from autoimmune cases, especially for therapeutic implications...
  8. doi request reprint Charcot-Marie-Tooth disease type 1B: marked phenotypic variation of the Ser78Leu mutation in five Italian families
    A Mazzeo
    Department of Neurosciences, Psychiatry and Anaesthesiology University of Messina, Messina, Italy
    Acta Neurol Scand 118:328-32. 2008
    ..To describe clinical, electrophysiological and genetic data of five unrelated Sicilian pedigrees harbouring a heterozygous Ser78Leu mutation in the myelin protein zero (MPZ) extracellular domain...
  9. ncbi request reprint Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies
    V Macaione
    Department of Biochemical, Physiological and Nutritional Sciences, University of Messina, Messina, Italy
    Acta Neurol Scand 117:393-8. 2008
    ..An increased transglutaminase 2 (TG2) expression has been found in DM, PM and s-IBM. The aim of our study was to investigate TG2 expression in FM in comparison with other IIM...
  10. doi request reprint ANT1 is reduced in sporadic inclusion body myositis
    E Barca
    Department of Neurosciences, Psychiatry and Anesthesiology, AOU G Martino, Messina, Italy
    Neurol Sci 34:217-24. 2013
    ..Normal ANT1 expression in PM could be related to the scarcity of mitochondrial abnormalities in the disease, but it could also suggest that these two conditions diverge in activating different anti-apoptotic pathways...
  11. ncbi request reprint Peripheral neuropathy as the presenting feature of multiple system atrophy
    C Rodolico
    Institute of Neurologic and Neurosurgical Sciences, University of Messina, Italy
    Clin Auton Res 11:119-21. 2001
    ....
  12. ncbi request reprint Cardiovascular autonomic control in Becker muscular dystrophy
    G Vita
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Messina, Italy
    J Neurol Sci 186:45-9. 2001
    ..PSA values were not influenced by age, functional ability score or presence of heart abnormalities. Our data suggest that autonomic involvement does not represent a major finding in BMD...
  13. ncbi request reprint RAGE-NF-kappaB pathway activation in response to oxidative stress in facioscapulohumeral muscular dystrophy
    V Macaione
    Department of Biochemical, Physiological and Nutritional Sciences, University of Messina, Messina, Italy
    Acta Neurol Scand 115:115-21. 2007
    ..Oxidative stress can stimulate RAGE- NF-kappaB pathway. Our purpose was to verify if oxidative stress may induce RAGE- NF-kappaB pathway activation in FSHD, contributing to the pathogenesis of such a disease...
  14. pmc Activation of NF-kappaB pathway in Duchenne muscular dystrophy: relation to age
    S Messina
    Department of Neurosciences, Psychiatry and Anaesthesiology, University of Messina, Italy
    Acta Myol 30:16-23. 2011
    ..Further studies on the interactions among these pathways in different DMD phases and on the response of these cascades to treatments currently under investigation are needed to better elucidate their relevance as therapeutic targets...
  15. ncbi request reprint Novel SHOX gene mutation in a short boy with Becker muscular dystrophy: double trouble in two adjacent genes
    M F Messina
    Department of Pediatrics, Psychiatry and Anesthesiology, University of Messina, Messina, Italy
    Horm Res 69:124-8. 2008
    ..1 SDS). Our data suggest that abnormal growth observed in a boy with BMD may be related to an additional genetic alteration, already known as correlated with short stature...
  16. ncbi request reprint Acute motor axonal polyneuropathy after a cisatracurium infusion and concomitant corticosteroid therapy
    V Fodale
    Section of Anesthesia and Intensive Care Unit, Department of Neuroscience, Psychiatric and Anesthesiological Sciences, University of Messina, Policlinico Universitario G Martino, I 98125 Messina, Italy
    Br J Anaesth 92:289-93. 2004
    ..Clinical symptoms and electrophysiological examinations supported the diagnosis of acute motor axonal polyneuropathy related to concomitant administration of cisatracurium and corticosteroid therapy...
  17. ncbi request reprint Phenotypic clustering of lamin A/C mutations in neuromuscular patients
    S Benedetti
    Laboratory of Clinical Molecular Biology DIBIT 2, Diagnostics and Research San Raffaele, Milan, Italy
    Neurology 69:1285-92. 2007
    ..Mutations in the LMNA gene, encoding human lamin A/C, have been associated with an increasing number of disorders often involving skeletal and cardiac muscle, but no clear genotype/phenotype correlation could be established to date...
  18. ncbi request reprint Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL
    S Lucchiari
    Dino Ferrari Center, Department of Neurological Sciences, University of Milan, Fondazione I R C C S Ospedale Maggiore Policlinico, Mangialli, Regina Elena, Milan, Italy
    Hum Mutat 27:600-1. 2006
    ..664+3A>G was also detected in two patients, both homozygous. The present work is yet another confirmation that the individual genetic background plays a pivotal role in influencing the phenotypes, as occurs in other metabolic diseases...
  19. ncbi request reprint Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population
    R Cagliani
    IRCCS E Medea, Associazione La Nostra Famiglia, Via Don Luigi Monza 20, 23842 Bosisio Parini LC, Italy
    Neuromuscul Disord 13:788-95. 2003
    ..The possible existence of a founder effect for the Arg959Trp mutation in the Italian population is discussed...
  20. pmc Chiari I malformation mimicking myasthenia gravis
    C Rodolico
    J Neurol Neurosurg Psychiatry 74:393. 2003