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G Novelli

Showing results (51-60 of 330) with videos related to

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Contributions to Nephrology|June 4, 2010
Early management of endotoxemia using the endotoxin activity assay and polymyxin B-based hemoperfusionG Novelli, G Ferretti, F Ruberto, et al.
Molecular and Cellular Probes|January 18, 2005
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian populationL Vallo, E Bonifazi, P Borgiani, et al.
Minerva Stomatologica|April 8, 2014
Vacuum assisted closure therapy in the management of cervico-facial necrotizing fasciitis: a case report and review of the literatureG Novelli, S Catanzaro, G Canzi, et al.
Human Heredity|January 1, 1986
Increased erythrocyte adenosine deaminase activity without haemolytic anaemiaG Novelli, V Stocchi, A Giannotti, et al.
Neuromuscular Disorders : NMD|March 1, 1995
Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeatsG Novelli, M Gennarelli, E Menegazzo, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 4, 1998
A single polymerase chain reaction-based protocol for detecting normal and expanded alleles in myotonic dystrophyM Gennarelli, M Pavoni, P Amicucci, et al.
Minerva Anestesiologica|January 13, 2006
Patient-controlled analgesia with tramadol versus tramadol plus ketorolacA Lepri, S Sia, S Catinelli, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Yq deletions and AZF locus: molecular analysis in two fetuses with non familial homogeneous Yq rearrangementsL Camurri, G Novelli, M Gennarelli, et al.
American Journal of Medical Genetics|January 1, 1985
Red blood cell adenine nucleotides abnormalities in Down syndromeV Stocchi, M Magnani, L Cucchiarini, et al.
Clinical Physiology and Biochemistry|January 1, 1987
Red blood cell glucose metabolism in Down's syndromeM Magnani, V Stocchi, G Novelli, et al.
Pageof 33

Showing results (51-60 of 330) with videos related to

Sort By:
Pageof 33
Contributions to Nephrology|June 4, 2010
Early management of endotoxemia using the endotoxin activity assay and polymyxin B-based hemoperfusionG Novelli, G Ferretti, F Ruberto, et al.
Molecular and Cellular Probes|January 18, 2005
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian populationL Vallo, E Bonifazi, P Borgiani, et al.
Minerva Stomatologica|April 8, 2014
Vacuum assisted closure therapy in the management of cervico-facial necrotizing fasciitis: a case report and review of the literatureG Novelli, S Catanzaro, G Canzi, et al.
Human Heredity|January 1, 1986
Increased erythrocyte adenosine deaminase activity without haemolytic anaemiaG Novelli, V Stocchi, A Giannotti, et al.
Neuromuscular Disorders : NMD|March 1, 1995
Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeatsG Novelli, M Gennarelli, E Menegazzo, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|December 4, 1998
A single polymerase chain reaction-based protocol for detecting normal and expanded alleles in myotonic dystrophyM Gennarelli, M Pavoni, P Amicucci, et al.
Minerva Anestesiologica|January 13, 2006
Patient-controlled analgesia with tramadol versus tramadol plus ketorolacA Lepri, S Sia, S Catinelli, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Yq deletions and AZF locus: molecular analysis in two fetuses with non familial homogeneous Yq rearrangementsL Camurri, G Novelli, M Gennarelli, et al.
American Journal of Medical Genetics|January 1, 1985
Red blood cell adenine nucleotides abnormalities in Down syndromeV Stocchi, M Magnani, L Cucchiarini, et al.
Clinical Physiology and Biochemistry|January 1, 1987
Red blood cell glucose metabolism in Down's syndromeM Magnani, V Stocchi, G Novelli, et al.
Pageof 33