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S Servidei

Showing results (61-70 of 146) with videos related to

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Ultrastructural Pathology|September 1, 1992
Acute myopathy associated with chronic licorice ingestion: reversible loss of myoadenylate deaminase activityP Caradonna, N Gentiloni, S Servidei, et al.
European Journal of Neurology|January 30, 2016
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experienceM Luigetti, D Sauchelli, G Primiano, et al.
European Journal of Neurology|July 20, 2016
Mitochondrial neuropathy: considerations on pathogenesisM Luigetti, D Sauchelli, G Primiano, et al.
La Clinica Terapeutica|June 15, 2017
Recurrent miller fisher: a new case report and a literature reviewF Barbato, A Di Paolantonio, M Distefano, et al.
Acta Neurologica Scandinavica|June 1, 1992
Benign monomelic amyotrophy of lower limb: report of three casesA Uncini, S Servidei, C Delli Pizzi, et al.
International Journal of Immunopathology and Pharmacology|October 6, 2004
Association of myasthenia gravis and antisynthetase syndrome: a case reportM Diaco, F Ancarini, M Montalto, et al.
Italian Journal of Neurological Sciences|May 1, 1981
Clinical features of amyotrophic amyotrophic lateral sclerosisP David, M Lo Monaco, G Palieri, et al.
Archives of Neurology|October 1, 1990
X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemiaC L Warner, S Servidei, D J Lange, et al.
Neurogenetics|February 7, 2001
The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcriptionM Mirabella, S Servidei, A Broccolini, et al.
American Journal of Medical Genetics|September 20, 2000
Single-fiber PCR in MELAS(3243) patients: correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotypeG Silvestri, M Rana, F Odoardi, et al.
Pageof 15

Showing results (61-70 of 146) with videos related to

Sort By:
Pageof 15
Ultrastructural Pathology|September 1, 1992
Acute myopathy associated with chronic licorice ingestion: reversible loss of myoadenylate deaminase activityP Caradonna, N Gentiloni, S Servidei, et al.
European Journal of Neurology|January 30, 2016
Peripheral neuropathy is a common manifestation of mitochondrial diseases: a single-centre experienceM Luigetti, D Sauchelli, G Primiano, et al.
European Journal of Neurology|July 20, 2016
Mitochondrial neuropathy: considerations on pathogenesisM Luigetti, D Sauchelli, G Primiano, et al.
La Clinica Terapeutica|June 15, 2017
Recurrent miller fisher: a new case report and a literature reviewF Barbato, A Di Paolantonio, M Distefano, et al.
Acta Neurologica Scandinavica|June 1, 1992
Benign monomelic amyotrophy of lower limb: report of three casesA Uncini, S Servidei, C Delli Pizzi, et al.
International Journal of Immunopathology and Pharmacology|October 6, 2004
Association of myasthenia gravis and antisynthetase syndrome: a case reportM Diaco, F Ancarini, M Montalto, et al.
Italian Journal of Neurological Sciences|May 1, 1981
Clinical features of amyotrophic amyotrophic lateral sclerosisP David, M Lo Monaco, G Palieri, et al.
Archives of Neurology|October 1, 1990
X-linked spinal muscular atrophy (Kennedy's syndrome). A kindred with hypobetalipoproteinemiaC L Warner, S Servidei, D J Lange, et al.
Neurogenetics|February 7, 2001
The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcriptionM Mirabella, S Servidei, A Broccolini, et al.
American Journal of Medical Genetics|September 20, 2000
Single-fiber PCR in MELAS(3243) patients: correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotypeG Silvestri, M Rana, F Odoardi, et al.
Pageof 15