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L Chiadò-Piat

Showing results (1-10 of 26) with videos related to

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Clinical Neuropathology|May 1, 1993
Adult onset nemaline myopathy: a distinct nosologic entity?L Palmucci, C Doriguzzi, T Mongini, et al.
European Journal of Clinical Investigation|April 1, 1996
Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type)T Mongini, C Doriguzzi, L Palmucci, et al.
European Neurology|January 1, 1993
Clinical spectrum of McArdle disease: three cases with unusual expressionL Chiadò-Piat, T Mongini, C Doriguzzi, et al.
Neurology|February 11, 2000
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same familyL Palmucci, T Mongini, L Chiadò-Piat, et al.
European Neurology|November 24, 1999
Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathyL Palmucci, C Doriguzzi, T Mongini, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|October 23, 2001
Cyclin D1 expression in normal oligodendroglia and microglia cells: its use in the differential diagnosis of oligodendrogliomasI Bosone, P Cavalla, L Chiadò-Piat, et al.
Journal of Neuro-Oncology|February 1, 1996
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical studyD Schiffer, P Cavalla, A Migheli, et al.
Neuroscience Letters|February 15, 2001
Distribution of activated caspase-3 in relation with apoptosis in human malignant gliomasD Schiffer, V Fiano, L Chiadò-Piat, et al.
European Journal of Clinical Investigation|April 1, 1997
Systematic use of dystrophin testing in muscle biopsies: results in 201 casesC Doriguzzi, L Palmucci, T Mongini, et al.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Clinical Neuropathology|May 1, 1993
Adult onset nemaline myopathy: a distinct nosologic entity?L Palmucci, C Doriguzzi, T Mongini, et al.
European Journal of Clinical Investigation|April 1, 1996
Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type)T Mongini, C Doriguzzi, L Palmucci, et al.
European Neurology|January 1, 1993
Clinical spectrum of McArdle disease: three cases with unusual expressionL Chiadò-Piat, T Mongini, C Doriguzzi, et al.
Neurology|February 11, 2000
Dystrophinopathy expressing as either cardiomyopathy or Becker dystrophy in the same familyL Palmucci, T Mongini, L Chiadò-Piat, et al.
European Neurology|November 24, 1999
Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathyL Palmucci, C Doriguzzi, T Mongini, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|October 23, 2001
Cyclin D1 expression in normal oligodendroglia and microglia cells: its use in the differential diagnosis of oligodendrogliomasI Bosone, P Cavalla, L Chiadò-Piat, et al.
Journal of Neuro-Oncology|February 1, 1996
Bcl-2 distribution in neuroepithelial tumors: an immunohistochemical studyD Schiffer, P Cavalla, A Migheli, et al.
Neuroscience Letters|February 15, 2001
Distribution of activated caspase-3 in relation with apoptosis in human malignant gliomasD Schiffer, V Fiano, L Chiadò-Piat, et al.
European Journal of Clinical Investigation|April 1, 1997
Systematic use of dystrophin testing in muscle biopsies: results in 201 casesC Doriguzzi, L Palmucci, T Mongini, et al.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Pageof 3