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L Palmucci

Showing results (51-60 of 77) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1975
Soradic ulcerative mutilating acropathy with imbalance of free amino acids in the cerebrospinal fluidF Monaco, A Riccio, A Covacich, et al.
Clinical Neuropathology|May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationT Mongini, C Doriguzzi, L Chiadò-Piat, 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.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
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.
Clinical Neuropathology|July 1, 1985
Spongiform encephalopathy in addicts inhaling pre-heated heroinD Schiffer, F Brignolio, M T Giordana, 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.
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.
Neuropediatrics|June 21, 2001
Myopathy in a patient with chromosome 22q11 deletionT Mongini, C Doriguzzi, C Arduino, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1975
Soradic ulcerative mutilating acropathy with imbalance of free amino acids in the cerebrospinal fluidF Monaco, A Riccio, A Covacich, et al.
Clinical Neuropathology|May 15, 2002
MERRF/MELAS overlap syndrome in a family with A3243G mtDNA mutationT Mongini, C Doriguzzi, L Chiadò-Piat, 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.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
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.
Clinical Neuropathology|July 1, 1985
Spongiform encephalopathy in addicts inhaling pre-heated heroinD Schiffer, F Brignolio, M T Giordana, 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.
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.
Neuropediatrics|June 21, 2001
Myopathy in a patient with chromosome 22q11 deletionT Mongini, C Doriguzzi, C Arduino, et al.
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