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C Doriguzzi

Showing results (31-40 of 55) with videos related to

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Neurology|March 1, 1994
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin geneL Palmucci, C Doriguzzi, T Mongini, 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.
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.
Neuropediatrics|June 21, 2001
Myopathy in a patient with chromosome 22q11 deletionT Mongini, C Doriguzzi, C Arduino, et al.
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.
Minerva Medica|September 15, 1980
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]C Doriguzzi, A Bertolotto, T Mongini, et al.
Italian Journal of Orthopaedics and Traumatology|December 1, 1984
Histomorphometric study of the dynamics of mineralization in a case of osteomalacia caused by anticonvulsants treated with 25(OH)d3M Portigliatti Barbos, P Rossi, A Jeantet, 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.
Pageof 6

Showing results (31-40 of 55) with videos related to

Sort By:
Pageof 6
Neurology|March 1, 1994
Unusual expression and very mild course of Xp21 muscular dystrophy (Becker type) in a 60-year-old man with 26 percent deletion of the dystrophin geneL Palmucci, C Doriguzzi, T Mongini, 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.
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.
Neuropediatrics|June 21, 2001
Myopathy in a patient with chromosome 22q11 deletionT Mongini, C Doriguzzi, C Arduino, et al.
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.
Minerva Medica|September 15, 1980
[Progressive muscular dystrophy of the Duchenne type. Epidemiology and strategy for prevention]C Doriguzzi, A Bertolotto, T Mongini, et al.
Italian Journal of Orthopaedics and Traumatology|December 1, 1984
Histomorphometric study of the dynamics of mineralization in a case of osteomalacia caused by anticonvulsants treated with 25(OH)d3M Portigliatti Barbos, P Rossi, A Jeantet, 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.
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