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T Mongini

Showing results (41-50 of 83) with videos related to

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Neuropediatrics|June 21, 2002
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuriaT Mongini, C Doriguzzi, I Bosone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiencyC Doriguzzi, L Palmucci, T Mongini, et al.
Journal of the Neurological Sciences|August 1, 1983
Laminin and fibronectin distribution in normal and pathological human muscleA Bertolotto, L Palmucci, C Doriguzzi, et al.
Neurogenetics|March 25, 2000
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory diseaseA Migheli, T Mongini, C Doriguzzi, et al.
European Journal of Histochemistry : EJH|January 1, 1994
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsiesC Doriguzzi, L Palmucci, T Mongini, et al.
Acta Neuropathologica|January 1, 1990
Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical studyC Doriguzzi, L Palmucci, B Pollo, et al.
Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.
Acta Neuropathologica|June 23, 1999
Variable histological expression of dystrophinopathy in two femalesC Doriguzzi, L Palmucci, T Mongini, et al.
Minerva Pediatrica|August 31, 1986
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods]C Doriguzzi, L Palmucci, T Mongini, et al.
Neurology|March 1, 1988
Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patientsT Mongini, D Ghigo, C Doriguzzi, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
Neuropediatrics|June 21, 2002
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuriaT Mongini, C Doriguzzi, I Bosone, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1989
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiencyC Doriguzzi, L Palmucci, T Mongini, et al.
Journal of the Neurological Sciences|August 1, 1983
Laminin and fibronectin distribution in normal and pathological human muscleA Bertolotto, L Palmucci, C Doriguzzi, et al.
Neurogenetics|March 25, 2000
Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory diseaseA Migheli, T Mongini, C Doriguzzi, et al.
European Journal of Histochemistry : EJH|January 1, 1994
Metachromatic dye-Ca++ATPase method in pathological muscle: a study of 382 muscle biopsiesC Doriguzzi, L Palmucci, T Mongini, et al.
Acta Neuropathologica|January 1, 1990
Cytochrome c oxidase and coenzyme Q in neuromuscular diseases: a histochemical studyC Doriguzzi, L Palmucci, B Pollo, et al.
Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.
Acta Neuropathologica|June 23, 1999
Variable histological expression of dystrophinopathy in two femalesC Doriguzzi, L Palmucci, T Mongini, et al.
Minerva Pediatrica|August 31, 1986
[Individualization of carriers of Duchenne's muscular dystrophy by quantitative methods]C Doriguzzi, L Palmucci, T Mongini, et al.
Neurology|March 1, 1988
Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patientsT Mongini, D Ghigo, C Doriguzzi, et al.
Pageof 9