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B Saitta

Showing results (31-40 of 262) with videos related to

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Cardiology in the Young|September 12, 2017
Atrial septal defect morphology and stenting in hypoplastic left heart syndrome after hybrid palliationLilia Oreto, Giuseppe Mandraffino, Lucia Manuri, et al.
European Neurology|January 1, 1993
Dopamine receptor SPET imaging in Parkinson's disease: a [123I]-IBZM and [99mTc]-HM-PAO studyG Pizzolato, F Chierichetti, A Rossato, et al.
Cardiology in the Young|March 11, 2017
Early hybrid approach and enteral feeding algorithm could reduce the incidence of necrotising enterocolitis in neonates with ductus-dependent systemic circulationLucia Manuri, Stefano Morelli, Salvatore Agati, et al.
Proceedings of the European Dialysis and Transplant Association - European Renal Association. European Dialysis and Transplant Association - European Renal Association. Congress|January 1, 1985
Radionuclear determination of glomerular filtration rate and renal plasma flow to detect early decrease of renal function in insulin dependent diabetesC Cascone, G Beltramello, N Borsato, et al.
The Journal of Nuclear Medicine and Allied Sciences|October 1, 1989
The quality control of SPET systems: results of an inter-laboratory comparison study in ItalyG Pedroli, A Crespi, A De Agostini, et al.
Neuromuscular Disorders : NMD|July 10, 1999
A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagenG Pepe, E Bertini, B Giusti, et al.
Genomics|September 1, 1991
Human clathrin heavy chain (CLTC): partial molecular cloning, expression, and mapping of the gene to human chromosome 17q11-qterG R Dodge, I Kovalszky, O W McBride, et al.
The Journal of Clinical Investigation|November 7, 2001
Role of protein kinase C-delta in the regulation of collagen gene expression in scleroderma fibroblastsS A Jimenez, S Gaidarova, B Saitta, et al.
Human Genetics|January 1, 1985
alpha alpha alpha anti-4.2 Haplotype and heterozygous beta null thalassemia in a Sicilian familyS Acuto, G Butticé, B Saitta, et al.
Biochemical and Biophysical Research Communications|May 18, 1999
A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha1(VI) collagen chain in an italian family affected by bethlem myopathyG Pepe, B Giusti, E Bertini, et al.
Pageof 27

Showing results (31-40 of 262) with videos related to

Sort By:
Pageof 27
Cardiology in the Young|September 12, 2017
Atrial septal defect morphology and stenting in hypoplastic left heart syndrome after hybrid palliationLilia Oreto, Giuseppe Mandraffino, Lucia Manuri, et al.
European Neurology|January 1, 1993
Dopamine receptor SPET imaging in Parkinson's disease: a [123I]-IBZM and [99mTc]-HM-PAO studyG Pizzolato, F Chierichetti, A Rossato, et al.
Cardiology in the Young|March 11, 2017
Early hybrid approach and enteral feeding algorithm could reduce the incidence of necrotising enterocolitis in neonates with ductus-dependent systemic circulationLucia Manuri, Stefano Morelli, Salvatore Agati, et al.
Proceedings of the European Dialysis and Transplant Association - European Renal Association. European Dialysis and Transplant Association - European Renal Association. Congress|January 1, 1985
Radionuclear determination of glomerular filtration rate and renal plasma flow to detect early decrease of renal function in insulin dependent diabetesC Cascone, G Beltramello, N Borsato, et al.
The Journal of Nuclear Medicine and Allied Sciences|October 1, 1989
The quality control of SPET systems: results of an inter-laboratory comparison study in ItalyG Pedroli, A Crespi, A De Agostini, et al.
Neuromuscular Disorders : NMD|July 10, 1999
A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagenG Pepe, E Bertini, B Giusti, et al.
Genomics|September 1, 1991
Human clathrin heavy chain (CLTC): partial molecular cloning, expression, and mapping of the gene to human chromosome 17q11-qterG R Dodge, I Kovalszky, O W McBride, et al.
The Journal of Clinical Investigation|November 7, 2001
Role of protein kinase C-delta in the regulation of collagen gene expression in scleroderma fibroblastsS A Jimenez, S Gaidarova, B Saitta, et al.
Human Genetics|January 1, 1985
alpha alpha alpha anti-4.2 Haplotype and heterozygous beta null thalassemia in a Sicilian familyS Acuto, G Butticé, B Saitta, et al.
Biochemical and Biophysical Research Communications|May 18, 1999
A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha1(VI) collagen chain in an italian family affected by bethlem myopathyG Pepe, B Giusti, E Bertini, et al.
Pageof 27