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Showing results (101-110 of 166) with videos related to

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Haematologica|March 11, 2008
Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemiaSilvia Galbiati, Barbara Foglieni, Maurizio Travi, et al.
Neurobiology of Aging|January 21, 2014
De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis caseAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
JAMA Neurology|July 16, 2014
Genome-wide analysis of the heritability of amyotrophic lateral sclerosisMargaux F Keller, Luigi Ferrucci, Andrew B Singleton, et al.
Neurobiology of Aging|July 6, 2010
A de novo missense mutation of the FUS gene in a "true" sporadic ALS caseAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.
The Journal of Pediatrics|May 19, 2009
The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemiaOrnella Guardamagna, Gabriella Restagno, Elio Rolfo, et al.
Genetic Testing|August 23, 2000
A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technologyG Restagno, A M Gomez, L Sbaiz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney diseaseA E Turco, S Rossetti, E Bresin, et al.
Critical Care (London, England)|June 5, 2015
Gut and sublingual microvascular effect of esmolol during septic shock in a porcine modelMatthias Jacquet-Lagrèze, Bernard Allaouchiche, Damien Restagno, et al.
Human Mutation|September 27, 2002
Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing lossAlessandro Ferraris, Eric Rappaport, Rosa Santacroce, et al.
Human Genetics|May 21, 2005
Fetal DNA detection in maternal plasma throughout gestationSilvia Galbiati, Maddalena Smid, Dania Gambini, et al.
Pageof 17

Showing results (101-110 of 166) with videos related to

Sort By:
Pageof 17
Haematologica|March 11, 2008
Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemiaSilvia Galbiati, Barbara Foglieni, Maurizio Travi, et al.
Neurobiology of Aging|January 21, 2014
De novo nonsense mutation of the FUS gene in an apparently familial amyotrophic lateral sclerosis caseAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
JAMA Neurology|July 16, 2014
Genome-wide analysis of the heritability of amyotrophic lateral sclerosisMargaux F Keller, Luigi Ferrucci, Andrew B Singleton, et al.
Neurobiology of Aging|July 6, 2010
A de novo missense mutation of the FUS gene in a "true" sporadic ALS caseAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.
The Journal of Pediatrics|May 19, 2009
The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemiaOrnella Guardamagna, Gabriella Restagno, Elio Rolfo, et al.
Genetic Testing|August 23, 2000
A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technologyG Restagno, A M Gomez, L Sbaiz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney diseaseA E Turco, S Rossetti, E Bresin, et al.
Critical Care (London, England)|June 5, 2015
Gut and sublingual microvascular effect of esmolol during septic shock in a porcine modelMatthias Jacquet-Lagrèze, Bernard Allaouchiche, Damien Restagno, et al.
Human Mutation|September 27, 2002
Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing lossAlessandro Ferraris, Eric Rappaport, Rosa Santacroce, et al.
Human Genetics|May 21, 2005
Fetal DNA detection in maternal plasma throughout gestationSilvia Galbiati, Maddalena Smid, Dania Gambini, et al.
Pageof 17