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T Mongini

Showing results (1-10 of 83) with videos related to

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Pathologica|January 1, 1983
[Progressive muscular dystrophy in childhood: differential diagnosis and prevention strategy]D Schiffer, C Doriguzzi, T Mongini
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1990
Body building and rhabdomyolysisC Doriguzzi, L Palmucci, T Mongini
Neurology|November 1, 1983
Interictal conduction slowing in muscle fibers in hypokalemic periodic paralysisW Troni, C Doriguzzi, T Mongini
Advances in Experimental Medicine and Biology|January 1, 1985
Hereditary metabolic myopathiesA F Miranda, T Mongini, S DiMauro
Clinical Neuropathology|January 1, 1984
Tubular aggregates in a case of osteomalacic myopathy due to anticonvulsant drugsC Doriguzzi, T Mongini, A Jeantet, et al.
Histochemistry|January 1, 1983
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typingC Doriguzzi, T Mongini, L Palmucci, et al.
Journal of Neurology|January 1, 1987
Early sarcolemmal dysfunction in skeletal muscle amyloidosisC Doriguzzi, T Mongini, W Troni, et al.
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.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1991
Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophyL Palmucci, T Mongini, C Doriguzzi, et al.
Pageof 9

Showing results (1-10 of 83) with videos related to

Sort By:
Pageof 9
Pathologica|January 1, 1983
[Progressive muscular dystrophy in childhood: differential diagnosis and prevention strategy]D Schiffer, C Doriguzzi, T Mongini
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1990
Body building and rhabdomyolysisC Doriguzzi, L Palmucci, T Mongini
Neurology|November 1, 1983
Interictal conduction slowing in muscle fibers in hypokalemic periodic paralysisW Troni, C Doriguzzi, T Mongini
Advances in Experimental Medicine and Biology|January 1, 1985
Hereditary metabolic myopathiesA F Miranda, T Mongini, S DiMauro
Clinical Neuropathology|January 1, 1984
Tubular aggregates in a case of osteomalacic myopathy due to anticonvulsant drugsC Doriguzzi, T Mongini, A Jeantet, et al.
Histochemistry|January 1, 1983
A new method for myofibrillar Ca++-ATPase reaction based on the use of metachromatic dyes: its advantages in muscle fibre typingC Doriguzzi, T Mongini, L Palmucci, et al.
Journal of Neurology|January 1, 1987
Early sarcolemmal dysfunction in skeletal muscle amyloidosisC Doriguzzi, T Mongini, W Troni, et al.
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.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1991
Familial autosomal recessive rigid spine syndrome with neurogenic facio-scapulo-peroneal muscle atrophyL Palmucci, T Mongini, C Doriguzzi, et al.
Pageof 9