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Journal of the Neurological Sciences
|
September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy
L Palmucci, C Doriguzzi, T Mongini, et al.
Journal of the Neurological Sciences
|
August 1, 1983
Laminin and fibronectin distribution in normal and pathological human muscle
A 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 disease
A Migheli, T Mongini, C Doriguzzi, 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 patients
T Mongini, D Ghigo, C Doriguzzi, et al.
Revue Neurologique
|
January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies
G Scarlato, N Bresolin, I Moroni, 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.
Acta Neuropathologica
|
June 23, 1999
Variable histological expression of dystrophinopathy in two females
C Doriguzzi, L Palmucci, T Mongini, et al.
European Neurology
|
January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case
T Mongini, C Doriguzzi, L Palmucci, et al.
Clinical Neuropathology
|
October 12, 2001
Late onset and very mild course of Xp21 Becker type muscular dystrophy
I Bosone, S Bortolotto, T Mongini, et al.
Italian Journal of Neurological Sciences
|
January 1, 1981
Epidemiology of Duchenne muscular dystrophy in the province of Turin
A Bertolotto, M De Marchi, C Doriguzzi, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Journal of the Neurological Sciences
|
September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy
L Palmucci, C Doriguzzi, T Mongini, et al.
Journal of the Neurological Sciences
|
August 1, 1983
Laminin and fibronectin distribution in normal and pathological human muscle
A 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 disease
A Migheli, T Mongini, C Doriguzzi, 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 patients
T Mongini, D Ghigo, C Doriguzzi, et al.
Revue Neurologique
|
January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies
G Scarlato, N Bresolin, I Moroni, 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.
Acta Neuropathologica
|
June 23, 1999
Variable histological expression of dystrophinopathy in two females
C Doriguzzi, L Palmucci, T Mongini, et al.
European Neurology
|
January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case
T Mongini, C Doriguzzi, L Palmucci, et al.
Clinical Neuropathology
|
October 12, 2001
Late onset and very mild course of Xp21 Becker type muscular dystrophy
I Bosone, S Bortolotto, T Mongini, et al.
Italian Journal of Neurological Sciences
|
January 1, 1981
Epidemiology of Duchenne muscular dystrophy in the province of Turin
A Bertolotto, M De Marchi, C Doriguzzi, et al.
Page
of 6