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F Invernizzi

Showing results (71-80 of 90) with videos related to

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Plos One|June 10, 2011
A template-dependent dislocation mechanism potentiates K65R reverse transcriptase mutation development in subtype C variants of HIV-1Dimitrios Coutsinos, Cédric F Invernizzi, Daniela Moisi, et al.
Neurology|January 29, 2003
Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiencyN Nardocci, G Zorzi, N Blau, et al.
Clinical and Experimental Rheumatology|November 1, 1995
HCV genotypes in bone marrow and peripheral blood mononuclear cells of patients with mixed cryoglobulinemiaG Zehender, C de Maddalena, G Monti, et al.
QJM : Monthly Journal of the Association of Physicians|February 1, 1995
Cryoglobulinaemias: a multi-centre study of the early clinical and laboratory manifestations of primary and secondary disease. GISC. Italian Group for the Study of CryoglobulinaemiasG Monti, M Galli, F Invernizzi, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutationsB Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.
Annali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|October 1, 1992
Hepatitis B virus-related markers in secondary and in essential mixed cryoglobulinemias: a multicentric study of 596 cases. The Italian Group for the Study of Cryoglobulinemias (GISC)M Galli, G Monti, F Invernizzi, et al.
Lancet (London, England)|April 18, 1992
Hepatitis C virus and mixed cryoglobulinaemiasM Galli, G Monti, A Monteverde, et al.
The Journal of Antimicrobial Chemotherapy|June 11, 2013
The preferential selection of K65R in HIV-1 subtype C is attenuated by nucleotide polymorphisms at thymidine analogue mutation sitesCédric F Invernizzi, Dimitrios Coutsinos, Maureen Oliveira, et al.
Human Mutation|May 26, 1998
Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypesK Wataya, J Akanuma, P Cavadini, et al.
The Journal of Infectious Diseases|March 1, 1995
Hepatitis C virus RNA in the bone marrow of patients with mixed cryoglobulinemia and in subjects with noncryoglobulinemic chronic hepatitis type CM Galli, G Zehender, G Monti, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
Plos One|June 10, 2011
A template-dependent dislocation mechanism potentiates K65R reverse transcriptase mutation development in subtype C variants of HIV-1Dimitrios Coutsinos, Cédric F Invernizzi, Daniela Moisi, et al.
Neurology|January 29, 2003
Neonatal dopa-responsive extrapyramidal syndrome in twins with recessive GTPCH deficiencyN Nardocci, G Zorzi, N Blau, et al.
Clinical and Experimental Rheumatology|November 1, 1995
HCV genotypes in bone marrow and peripheral blood mononuclear cells of patients with mixed cryoglobulinemiaG Zehender, C de Maddalena, G Monti, et al.
QJM : Monthly Journal of the Association of Physicians|February 1, 1995
Cryoglobulinaemias: a multi-centre study of the early clinical and laboratory manifestations of primary and secondary disease. GISC. Italian Group for the Study of CryoglobulinaemiasG Monti, M Galli, F Invernizzi, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutationsB Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.
Annali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|October 1, 1992
Hepatitis B virus-related markers in secondary and in essential mixed cryoglobulinemias: a multicentric study of 596 cases. The Italian Group for the Study of Cryoglobulinemias (GISC)M Galli, G Monti, F Invernizzi, et al.
Lancet (London, England)|April 18, 1992
Hepatitis C virus and mixed cryoglobulinaemiasM Galli, G Monti, A Monteverde, et al.
The Journal of Antimicrobial Chemotherapy|June 11, 2013
The preferential selection of K65R in HIV-1 subtype C is attenuated by nucleotide polymorphisms at thymidine analogue mutation sitesCédric F Invernizzi, Dimitrios Coutsinos, Maureen Oliveira, et al.
Human Mutation|May 26, 1998
Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypesK Wataya, J Akanuma, P Cavadini, et al.
The Journal of Infectious Diseases|March 1, 1995
Hepatitis C virus RNA in the bone marrow of patients with mixed cryoglobulinemia and in subjects with noncryoglobulinemic chronic hepatitis type CM Galli, G Zehender, G Monti, et al.
Pageof 9