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Agathe Roubertie

Showing results (1-10 of 139) with videos related to

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Journal of Child Neurology|May 4, 2004
Congenital club foot with survival of motor neuron 1, telomeric (SMN1) gene deletionBernard Echenne, François Rivier, Agathe Roubertie, et al.
Pediatric Neurology|July 4, 2006
Partial epilepsy and 47,XXX karyotype: report of four casesAgathe Roubertie, Véronique Humbertclaude, Julie Leydet, et al.
Cephalalgia : an International Journal of Headache|September 21, 2010
Benign paroxysmal vertigo of childhood: long-term outcomeBenjamin Krams, Bernard Echenne, Julie Leydet, et al.
Epilepsia|June 7, 2003
Interictal paroxysmal epileptic discharges during sleep in childhood: phenotypic variability in a familyAgathe Roubertie, Véronique Humbertclaude, François Rivier, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 10, 2008
Monoamine metabolism study in severe, early-onset epilepsy in childhoodBernard Echenne, Agathe Roubertie, Julie Leydet, et al.
Brain & Development|August 9, 2003
Ataxia with vitamin E deficiency and severe dystonia: report of a caseAgathe Roubertie, Brigitte Biolsi, François Rivier, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 26, 2007
Myotonic dystrophy type I in childhood Long-term evolution in patients surviving the neonatal periodBernard Echenne, Aline Rideau, Agathe Roubertie, et al.
Journal of the American Academy of Dermatology|May 16, 2017
Long-term treatment of cutaneous manifestations of tuberous sclerosis complex with topical 1% sirolimus cream: A prospective study of 25 patientsNausicaa Malissen, Laurence Vergely, Marguerite Simon, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|April 30, 2016
Role of neuroimaging in the diagnosis of hereditary cerebellar ataxias in childhoodGiulia Perucca, Nicolas Leboucq, Agathe Roubertie, et al.
Frontiers in Genetics|November 6, 2015
A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disabilityMajida Charif, Agathe Roubertie, Sara Salime, et al.
Pageof 14

Showing results (1-10 of 139) with videos related to

Sort By:
Pageof 14
Journal of Child Neurology|May 4, 2004
Congenital club foot with survival of motor neuron 1, telomeric (SMN1) gene deletionBernard Echenne, François Rivier, Agathe Roubertie, et al.
Pediatric Neurology|July 4, 2006
Partial epilepsy and 47,XXX karyotype: report of four casesAgathe Roubertie, Véronique Humbertclaude, Julie Leydet, et al.
Cephalalgia : an International Journal of Headache|September 21, 2010
Benign paroxysmal vertigo of childhood: long-term outcomeBenjamin Krams, Bernard Echenne, Julie Leydet, et al.
Epilepsia|June 7, 2003
Interictal paroxysmal epileptic discharges during sleep in childhood: phenotypic variability in a familyAgathe Roubertie, Véronique Humbertclaude, François Rivier, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 10, 2008
Monoamine metabolism study in severe, early-onset epilepsy in childhoodBernard Echenne, Agathe Roubertie, Julie Leydet, et al.
Brain & Development|August 9, 2003
Ataxia with vitamin E deficiency and severe dystonia: report of a caseAgathe Roubertie, Brigitte Biolsi, François Rivier, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 26, 2007
Myotonic dystrophy type I in childhood Long-term evolution in patients surviving the neonatal periodBernard Echenne, Aline Rideau, Agathe Roubertie, et al.
Journal of the American Academy of Dermatology|May 16, 2017
Long-term treatment of cutaneous manifestations of tuberous sclerosis complex with topical 1% sirolimus cream: A prospective study of 25 patientsNausicaa Malissen, Laurence Vergely, Marguerite Simon, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|April 30, 2016
Role of neuroimaging in the diagnosis of hereditary cerebellar ataxias in childhoodGiulia Perucca, Nicolas Leboucq, Agathe Roubertie, et al.
Frontiers in Genetics|November 6, 2015
A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disabilityMajida Charif, Agathe Roubertie, Sara Salime, et al.
Pageof 14