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F Invernizzi

Showing results (61-70 of 90) with videos related to

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Journal of Neuroimmunology|March 1, 1997
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathyB Bonetti, F Invernizzi, N Rizzuto, et al.
Journal of Medical Genetics|November 25, 2003
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her sonG Puoti, F Carrara, S Sampaolo, et al.
Journal of Medical Genetics|May 4, 2004
Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genomeA Limongelli, J Schaefer, S Jackson, et al.
La Ricerca in Clinica E in Laboratorio|April 1, 1986
Cryoglobulins and infectious diseasesM Galli, F Invernizzi, M Chemotti, et al.
Journal of Virology|December 17, 2008
Template usage is responsible for the preferential acquisition of the K65R reverse transcriptase mutation in subtype C variants of human immunodeficiency virus type 1Dimitrios Coutsinos, Cédric F Invernizzi, Hongtao Xu, et al.
Neuroreport|January 6, 1999
Retroviral-mediated transfer of the galactocerebrosidase gene in neural progenitor cellsE Torchiana, L Lulli, E Cattaneo, et al.
AIDS (London, England)|April 7, 2007
Arginine methylation of the HIV-1 nucleocapsid protein results in its diminished functionCédric F Invernizzi, Baode Xie, Fernando A Frankel, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatmentR Parini, F Invernizzi, F Menni, et al.
Clinical and Experimental Immunology|August 1, 1986
In vitro synthesis of IgM rheumatoid factor by lymphocytes from patients with essential mixed cryoglobulinemiaP L Meroni, W Barcellini, R A Sinico, et al.
Pageof 9

Showing results (61-70 of 90) with videos related to

Sort By:
Pageof 9
Journal of Neuroimmunology|March 1, 1997
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathyB Bonetti, F Invernizzi, N Rizzuto, et al.
Journal of Medical Genetics|November 25, 2003
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her sonG Puoti, F Carrara, S Sampaolo, et al.
Journal of Medical Genetics|May 4, 2004
Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genomeA Limongelli, J Schaefer, S Jackson, et al.
La Ricerca in Clinica E in Laboratorio|April 1, 1986
Cryoglobulins and infectious diseasesM Galli, F Invernizzi, M Chemotti, et al.
Journal of Virology|December 17, 2008
Template usage is responsible for the preferential acquisition of the K65R reverse transcriptase mutation in subtype C variants of human immunodeficiency virus type 1Dimitrios Coutsinos, Cédric F Invernizzi, Hongtao Xu, et al.
Neuroreport|January 6, 1999
Retroviral-mediated transfer of the galactocerebrosidase gene in neural progenitor cellsE Torchiana, L Lulli, E Cattaneo, et al.
AIDS (London, England)|April 7, 2007
Arginine methylation of the HIV-1 nucleocapsid protein results in its diminished functionCédric F Invernizzi, Baode Xie, Fernando A Frankel, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuriaC Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease|September 3, 1999
Medium-chain triglyceride loading test in carnitine-acylcarnitine translocase deficiency: insights on treatmentR Parini, F Invernizzi, F Menni, et al.
Clinical and Experimental Immunology|August 1, 1986
In vitro synthesis of IgM rheumatoid factor by lymphocytes from patients with essential mixed cryoglobulinemiaP L Meroni, W Barcellini, R A Sinico, et al.
Pageof 9