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Showing results (61-70 of 166) with videos related to

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Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 6, 2009
Ovarian hyper-stimulation syndrome after spontaneous conceptionCristina Lussiana, Benedetta Guani, Gabriella Restagno, et al.
Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.
Transplantation Proceedings|September 17, 2013
A case report of AA amyloidosis associated with familial periodic fever syndrome diagnosed after kidney transplantation: never say neverM Messina, G Daidola, G Restagno, et al.
Clinical Chemistry and Laboratory Medicine|October 30, 2013
Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case reportSilvia Galbiati, Stefania Stenirri, Luca Sbaiz, et al.
Physical Review Letters|December 10, 2013
Effect of surface elasticity on the rheology of nanometric liquidsRichard Villey, Emmanuelle Martinot, Cécile Cottin-Bizonne, et al.
Human Reproduction (Oxford, England)|August 1, 1988
The dygynic origin of a triploid fetus from an IVF pregnancyG Restagno, G Ponzio, A Di Gregorio, et al.
Physical Review Letters|January 23, 2016
Self-Amplification of Solid Friction in Interleaved AssembliesHéctor Alarcón, Thomas Salez, Christophe Poulard, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 23, 2005
The IVS1 +319 t>a of SOD1 gene is not an ALS causing mutationG Restagno, A Gomez, F Lombardo, et al.
Haematologica|July 1, 1992
Carrier detection for prenatal diagnosis of hemophilia A in Italian familiesN Cappello, G Restagno, S Garnerone, et al.
The Journal of Urology|July 12, 2005
Low renin-angiotensin system activity gene polymorphism and dysplasia associated with posterior urethral valvesLicia Peruzzi, Federica Lombardo, Alessandro Amore, et al.
Pageof 17

Showing results (61-70 of 166) with videos related to

Sort By:
Pageof 17
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|June 6, 2009
Ovarian hyper-stimulation syndrome after spontaneous conceptionCristina Lussiana, Benedetta Guani, Gabriella Restagno, et al.
Journal of the Neurological Sciences|September 1, 1992
Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophyL Palmucci, C Doriguzzi, T Mongini, et al.
Transplantation Proceedings|September 17, 2013
A case report of AA amyloidosis associated with familial periodic fever syndrome diagnosed after kidney transplantation: never say neverM Messina, G Daidola, G Restagno, et al.
Clinical Chemistry and Laboratory Medicine|October 30, 2013
Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case reportSilvia Galbiati, Stefania Stenirri, Luca Sbaiz, et al.
Physical Review Letters|December 10, 2013
Effect of surface elasticity on the rheology of nanometric liquidsRichard Villey, Emmanuelle Martinot, Cécile Cottin-Bizonne, et al.
Human Reproduction (Oxford, England)|August 1, 1988
The dygynic origin of a triploid fetus from an IVF pregnancyG Restagno, G Ponzio, A Di Gregorio, et al.
Physical Review Letters|January 23, 2016
Self-Amplification of Solid Friction in Interleaved AssembliesHéctor Alarcón, Thomas Salez, Christophe Poulard, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 23, 2005
The IVS1 +319 t>a of SOD1 gene is not an ALS causing mutationG Restagno, A Gomez, F Lombardo, et al.
Haematologica|July 1, 1992
Carrier detection for prenatal diagnosis of hemophilia A in Italian familiesN Cappello, G Restagno, S Garnerone, et al.
The Journal of Urology|July 12, 2005
Low renin-angiotensin system activity gene polymorphism and dysplasia associated with posterior urethral valvesLicia Peruzzi, Federica Lombardo, Alessandro Amore, et al.
Pageof 17