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Massimo Pandolfo

Showing results (31-40 of 177) with videos related to

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Molecular Medicine (Cambridge, Mass.)|January 18, 2007
Real-time PCR and linkage studies to identify carriers presenting HPRT deleted geneCristina Lapucci, Diego Pomarè Montin, Massimo Pandolfo, et al.
The Cochrane Database of Systematic Reviews|April 20, 2012
Antioxidants and other pharmacological treatments for Friedreich ataxiaMary Kearney, Richard W Orrell, Michael Fahey, et al.
Movement Disorders Clinical Practice|January 11, 2021
Hand Dexterity and Pyramidal Dysfunction in Friedreich Ataxia, A Finger Tapping StudyGilles Naeije, Antonin Rovai, Massimo Pandolfo, et al.
The Cochrane Database of Systematic Reviews|October 13, 2009
Antioxidants and other pharmacological treatments for Friedreich ataxiaMary Kearney, Richard W Orrell, Michael Fahey, et al.
Neurology. Genetics|April 23, 2021
<i>Neurology: Genetics</i> Year in ReviewStefan Pulst, Massimo Pandolfo, Raymond Roos, et al.
European Neurology|August 1, 2008
The neurological presentation of ceruloplasmin gene mutationsAlisdair McNeill, Massimo Pandolfo, Jens Kuhn, et al.
European Heart Journal. Cardiovascular Imaging|December 1, 2011
Normal left ventricular ejection fraction and mass but subclinical myocardial dysfunction in patients with Friedreich's ataxiaChantal Dedobbeleer, Myriam Rai, Erwan Donal, et al.
Headache|March 29, 2014
Transient CNS deficits and migrainous auras in individuals without a history of headacheGilles Naeije, Nicolas Gaspard, Benjamin Legros, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|June 29, 2004
Recurrent transient ischemic attacks in a patient with intrapulmonary arteriovenous shunting detected after closure of a patent foramen ovalePhilippe Unger, Eric Stoupel, Shahab Shadfar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2004
Striking intrafamilial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the FRDA1 geneAmanpreet Badhwar, An Jansen, Frederick Andermann, et al.
Pageof 18

Showing results (31-40 of 177) with videos related to

Sort By:
Pageof 18
Molecular Medicine (Cambridge, Mass.)|January 18, 2007
Real-time PCR and linkage studies to identify carriers presenting HPRT deleted geneCristina Lapucci, Diego Pomarè Montin, Massimo Pandolfo, et al.
The Cochrane Database of Systematic Reviews|April 20, 2012
Antioxidants and other pharmacological treatments for Friedreich ataxiaMary Kearney, Richard W Orrell, Michael Fahey, et al.
Movement Disorders Clinical Practice|January 11, 2021
Hand Dexterity and Pyramidal Dysfunction in Friedreich Ataxia, A Finger Tapping StudyGilles Naeije, Antonin Rovai, Massimo Pandolfo, et al.
The Cochrane Database of Systematic Reviews|October 13, 2009
Antioxidants and other pharmacological treatments for Friedreich ataxiaMary Kearney, Richard W Orrell, Michael Fahey, et al.
Neurology. Genetics|April 23, 2021
<i>Neurology: Genetics</i> Year in ReviewStefan Pulst, Massimo Pandolfo, Raymond Roos, et al.
European Neurology|August 1, 2008
The neurological presentation of ceruloplasmin gene mutationsAlisdair McNeill, Massimo Pandolfo, Jens Kuhn, et al.
European Heart Journal. Cardiovascular Imaging|December 1, 2011
Normal left ventricular ejection fraction and mass but subclinical myocardial dysfunction in patients with Friedreich's ataxiaChantal Dedobbeleer, Myriam Rai, Erwan Donal, et al.
Headache|March 29, 2014
Transient CNS deficits and migrainous auras in individuals without a history of headacheGilles Naeije, Nicolas Gaspard, Benjamin Legros, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|June 29, 2004
Recurrent transient ischemic attacks in a patient with intrapulmonary arteriovenous shunting detected after closure of a patent foramen ovalePhilippe Unger, Eric Stoupel, Shahab Shadfar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2004
Striking intrafamilial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the FRDA1 geneAmanpreet Badhwar, An Jansen, Frederick Andermann, et al.
Pageof 18