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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
September 24, 2009
Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk
C Lamperti, M Zeviani
Muscle & Nerve
|
July 6, 2001
Muscle glycogenoses
S DiMauro, C Lamperti
Gene Therapy
|
July 29, 2017
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome
I Di Meo, S Marchet, C Lamperti, et al.
Microbiologica
|
April 1, 1990
Polarization and capping of lymphocytes in HIV infection
D Torre, A Pugliese, C Lamperti, et al.
European Cytokine Network
|
November 1, 1992
Effects of interleukin-8 on suppression of human lymphocyte polarization and migration by anti-LFA-1 antibody
D Torre, G Ferrario, C Lamperti, et al.
Neurology
|
February 13, 2002
Women with pregnancy-related polymyositis and high serum CK levels in the newborn
S Messina, G Fagiolari, C Lamperti, et al.
Journal of the Neurological Sciences
|
October 16, 2007
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency
S Corti, A Bordoni, D Ronchi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 5, 2008
An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report
L Tremolizzo, A Galbussera, E Tagliabue, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 20, 2012
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation
Enrico Saracchi, J C Difrancesco, L Brighina, et al.
Neurology
|
March 10, 2004
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency
M Gironi, C Lamperti, R Nemni, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 23) with videos related to
Sort By:
Page
of 3
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
September 24, 2009
Encephalomyopathies caused by abnormal nuclear-mitochondrial intergenomic cross-talk
C Lamperti, M Zeviani
Muscle & Nerve
|
July 6, 2001
Muscle glycogenoses
S DiMauro, C Lamperti
Gene Therapy
|
July 29, 2017
AAV9-based gene therapy partially ameliorates the clinical phenotype of a mouse model of Leigh syndrome
I Di Meo, S Marchet, C Lamperti, et al.
Microbiologica
|
April 1, 1990
Polarization and capping of lymphocytes in HIV infection
D Torre, A Pugliese, C Lamperti, et al.
European Cytokine Network
|
November 1, 1992
Effects of interleukin-8 on suppression of human lymphocyte polarization and migration by anti-LFA-1 antibody
D Torre, G Ferrario, C Lamperti, et al.
Neurology
|
February 13, 2002
Women with pregnancy-related polymyositis and high serum CK levels in the newborn
S Messina, G Fagiolari, C Lamperti, et al.
Journal of the Neurological Sciences
|
October 16, 2007
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency
S Corti, A Bordoni, D Ronchi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 5, 2008
An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report
L Tremolizzo, A Galbussera, E Tagliabue, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 20, 2012
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation
Enrico Saracchi, J C Difrancesco, L Brighina, et al.
Neurology
|
March 10, 2004
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency
M Gironi, C Lamperti, R Nemni, et al.
Page
of 3