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L Palmucci

Showing results (61-70 of 77) with videos related to

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Journal of the Neurological Sciences|February 1, 1986
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, 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.
Journal of Neurology|January 1, 1985
Familial progressive external ophthalmoplegia with multisystem abnormalities: "new" features raising nosological problemsR Cantello, L Bergamini, W Troni, 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|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.
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.
Clinical Neuropathology|October 12, 2001
Late onset and very mild course of Xp21 Becker type muscular dystrophyI Bosone, S Bortolotto, T Mongini, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
Journal of the Neurological Sciences|February 1, 1986
Quantitative analysis of quadriceps muscle biopsy. Results in 7 definite and 45 possible carriers of Duchenne muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, 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.
Journal of Neurology|January 1, 1985
Familial progressive external ophthalmoplegia with multisystem abnormalities: "new" features raising nosological problemsR Cantello, L Bergamini, W Troni, 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|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.
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.
Clinical Neuropathology|October 12, 2001
Late onset and very mild course of Xp21 Becker type muscular dystrophyI Bosone, S Bortolotto, T Mongini, et al.
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