V Sansone

Summary

Affiliation: University of Milan
Country: Italy

Publications

  1. ncbi request reprint Hypothyroidism unmasking proximal myotonic myopathy
    V Sansone
    Department of Neurology, University of Milan, San Donato Hospital, Via Morandi, 30, 20097 San Donato Milanese, Milan, Italy
    Neuromuscul Disord 10:165-72. 2000
  2. ncbi request reprint Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies
    R Cardani
    Department of Molecular Biology and Biotechnologies, University of Milan, Italy
    Eur J Histochem 53:107-11. 2009
  3. ncbi request reprint Therapy in myotonic disorders and in muscle channelopathies
    G Meola
    Department of Neurology, University of Milan, Istituto Policlinico San Donato, San Donato Milanese MI, Italy
    Neurol Sci 21:S953-61. 2000
  4. ncbi request reprint Cognitive impairment in adult myotonic dystrophies: a longitudinal study
    V Sansone
    Department of Neurology, University of Milan, IRCCS Policlinico San Donato, Via Morandi 30, I 20097 San Donato Milanese, Italy
    Neurol Sci 28:9-15. 2007
  5. ncbi request reprint Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2
    R Cardani
    Department of Molecular Biology and Biotechnologies, University of Milan, Italy
    Eur J Histochem 50:177-82. 2006
  6. ncbi request reprint Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)
    G Meola
    Department of Neurology, University of Milan, San Donato Hospital, Via Morandi 30, San Donato Milanese, 20097 Milan, Italy
    Neuromuscul Disord 13:813-21. 2003
  7. ncbi request reprint Influence on chondrogenesis of human osteoarthritic chondrocytes in co-culture with donor-matched mesenchymal stem cells from infrapatellar fat pad and subcutaneous adipose tissue
    S Lopa
    Cell and Tissue Engineering Laboratory, Gruppo Ospedaliero San Donato Foundation, Milan, Italy
    Int J Immunopathol Pharmacol 26:23-31. 2013
  8. ncbi request reprint Treatment in myotonia and periodic paralysis
    G Meola
    Department of Neurology, University of Milan, Istituto Policlinico San Donato, Italy
    Rev Neurol (Paris) 160:S55-69. 2004
  9. doi request reprint Low frequency pulsed electromagnetic field affects proliferation, tissue-specific gene expression, and cytokines release of human tendon cells
    L De Girolamo
    Orthopaedic Biotechnologies Laboratory, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy
    Cell Biochem Biophys 66:697-708. 2013
  10. ncbi request reprint Proximal myotonic myopathy: a syndrome with a favourable prognosis?
    Giovanni Meola
    Department of Neurology, University of Milan, Istituto Policlinico San Donato, Via Morandi, 30 20097, San Donato Milanese, Milan, Italy
    J Neurol Sci 193:89-96. 2002

Collaborators

Detail Information

Publications20

  1. ncbi request reprint Hypothyroidism unmasking proximal myotonic myopathy
    V Sansone
    Department of Neurology, University of Milan, San Donato Hospital, Via Morandi, 30, 20097 San Donato Milanese, Milan, Italy
    Neuromuscul Disord 10:165-72. 2000
    ..Other cases of 'hypothyroid myopathy' may represent examples of unmasked PROMM...
  2. ncbi request reprint Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies
    R Cardani
    Department of Molecular Biology and Biotechnologies, University of Milan, Italy
    Eur J Histochem 53:107-11. 2009
    ....
  3. ncbi request reprint Therapy in myotonic disorders and in muscle channelopathies
    G Meola
    Department of Neurology, University of Milan, Istituto Policlinico San Donato, San Donato Milanese MI, Italy
    Neurol Sci 21:S953-61. 2000
    ..Future genotype-phenotype correlations using the patch-clamp technique are also illustrated...
  4. ncbi request reprint Cognitive impairment in adult myotonic dystrophies: a longitudinal study
    V Sansone
    Department of Neurology, University of Milan, IRCCS Policlinico San Donato, Via Morandi 30, I 20097 San Donato Milanese, Italy
    Neurol Sci 28:9-15. 2007
    ..01), in both DM1 and DM2. DM2 is a progressive muscle disorder, although less severe than DM1. In both DM1 and DM2 frontal cognitive impairment (attentional) worsens over time but does not extend to additional areas of cognition...
  5. ncbi request reprint Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2
    R Cardani
    Department of Molecular Biology and Biotechnologies, University of Milan, Italy
    Eur J Histochem 50:177-82. 2006
    ..These findings indicate that MBNLs might be important targets for therapeutic interventions to correct some of the specific features of DM pathology...
  6. ncbi request reprint Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)
    G Meola
    Department of Neurology, University of Milan, San Donato Hospital, Via Morandi 30, San Donato Milanese, 20097 Milan, Italy
    Neuromuscul Disord 13:813-21. 2003
    ..The results suggest that there is a specific cognitive and behavioural profile in PROMM/DM-2 and in DM-1, and that this profile is associated with hypoperfusion in frontal and parieto-occipital regions of the brain...
  7. ncbi request reprint Influence on chondrogenesis of human osteoarthritic chondrocytes in co-culture with donor-matched mesenchymal stem cells from infrapatellar fat pad and subcutaneous adipose tissue
    S Lopa
    Cell and Tissue Engineering Laboratory, Gruppo Ospedaliero San Donato Foundation, Milan, Italy
    Int J Immunopathol Pharmacol 26:23-31. 2013
    ....
  8. ncbi request reprint Treatment in myotonia and periodic paralysis
    G Meola
    Department of Neurology, University of Milan, Istituto Policlinico San Donato, Italy
    Rev Neurol (Paris) 160:S55-69. 2004
    ....
  9. doi request reprint Low frequency pulsed electromagnetic field affects proliferation, tissue-specific gene expression, and cytokines release of human tendon cells
    L De Girolamo
    Orthopaedic Biotechnologies Laboratory, IRCCS Istituto Ortopedico Galeazzi, Milan, Italy
    Cell Biochem Biophys 66:697-708. 2013
    ....
  10. ncbi request reprint Proximal myotonic myopathy: a syndrome with a favourable prognosis?
    Giovanni Meola
    Department of Neurology, University of Milan, Istituto Policlinico San Donato, Via Morandi, 30 20097, San Donato Milanese, Milan, Italy
    J Neurol Sci 193:89-96. 2002
    ..Further studies of subgroups of PROMM (linked to the 3q21 locus and without linkage) are necessary to determine whether the cardiac conduction disturbances are more common in a specific genotype of PROMM...
  11. ncbi request reprint Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency
    R Lanzi
    Endocrinology Unit, Department of Internal Medicine, San Raffaele Scientific Institute and Universita Vita Salute San Raffaele, Milan, Italy
    J Endocrinol Invest 30:341-5. 2007
    ....
  12. pmc Glucose metabolism and dopamine PET correlates in a patient with myotonic dystrophy type 2 and parkinsonism
    V Sansone
    J Neurol Neurosurg Psychiatry 77:425-6. 2006
  13. ncbi request reprint Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy
    R Cardani
    Dipartimento di Fisiologia e Biochimica Generali, Universita di Milano, Italy
    Eur J Histochem 48:437-42. 2004
    ..Moreover, the procedure is simple, and readily applicable in any pathology laboratory...
  14. ncbi request reprint Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathies
    G Meola
    Istituto Policlinico San Donato, Dipartimento di Neurologia, Cattedra di Clinica Neurologica, Universita di Milano, Ospedale di San Donato, Italy
    Eur J Histochem 47:17-28. 2003
    ..DNA-based diagnosis is now a reality for many of the channelopathies. This has obvious genetic counselling, prognostic and therapeutic implications...
  15. ncbi request reprint Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2
    A Mankodi
    Department of Neurology, School of Medicine and Dentistry, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA
    Hum Mol Genet 10:2165-70. 2001
    ..These results support the idea that nuclear accumulation of mutant RNA is pathogenic in DM1, suggest that a similar disease process occurs in DM2, and point to a role for muscleblind in the pathogenesis of both disorders...
  16. ncbi request reprint The hypocretin neurotransmission system in myotonic dystrophy type 1
    E Ciafaloni
    University of Rochester, Department of Neurology, 601 Elmwood Avenue, Box 673, Rochester, NY 14642, USA
    Neurology 70:226-30. 2008
    ..Some patients with DM1 show sleep-onset REM, similar to that observed in narcolepsy. Narcolepsy is characterized by impaired hypocretin (Hcrt) neurotransmission...
  17. ncbi request reprint Persistent autobiographical amnesia: a case report
    C Repetto
    IRCCS San Giovanni di Dio FBF, Brescia, Italy
    Behav Neurol 18:13-7. 2007
    ..The absence of a clear pathomechanism underlying focal amnesia lead us to consider this case as an example of functional retrograde amnesia...
  18. ncbi request reprint Italian guidelines for molecular analysis in myotonic dystrophies
    A Botta
    Department of Biopatologia e Diagnostica per Immagini, Tor Vergata University, Rome, Italy
    Acta Myol 25:23-33. 2006
    ..Overviews of materials used in the molecular diagnosis, as well as internet resources, are also included...
  19. ncbi request reprint Proximal myotonic dystrophy mimicking progressive muscular atrophy
    G Rotondo
    Eur J Neurol 12:160-1. 2005
  20. ncbi request reprint Imaging of dopaminergic dysfunction with [123I]FP-CIT SPECT in early-onset parkin disease
    A Varrone
    Biostructure and Bioimaging Institute, National Research Council, Via S Pansini, 5, 80131, Napoli, Italy
    Neurology 63:2097-103. 2004
    ..To investigate whether the presence of parkin gene mutations is associated with different nigrostriatal impairment than other early-onset parkinsonism...