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Rima Nabbout

Showing results (281-290 of 310) with videos related to

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Epilepsia|April 3, 2016
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in FranceMathilde Chipaux, William Szurhaj, Laurent Vercueil, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 27, 2018
Renal angiomyolipoma in patients with tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increase disease AwarenessJ Chris Kingswood, Elena Belousova, Mirjana P Benedik, et al.
Epilepsia|January 27, 2024
Which terms should be used to describe medications used in the treatment of seizure disorders? An ILAE position paperEmilio Perucca, Jacqueline A French, Ghaieb Aljandeel, et al.
Frontiers in Neurology|April 9, 2021
TuberOus SClerosis registry to increAse disease awareness (TOSCA) Post-Authorisation Safety Study of Everolimus in Patients With Tuberous Sclerosis ComplexJ Chris Kingswood, Elena Belousova, Mirjana P Benedik, et al.
Frontiers in Neurology|September 28, 2020
Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA StudyAnna C Jansen, Stephanie Vanclooster, Petrus J de Vries, et al.
Orphanet Journal of Rare Diseases|March 12, 2025
Gynecological issues in children and adolescents seen at rare-disease referral centers: an observational retrospective cohort studyIphigénie Cavadias, Magali Viaud, Marie Falampin, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Genetics of epilepsy: epilepsy research foundation workshop reportSanjay Sisodiya, J Helen Cross, Ingmar Blümcke, et al.
American Journal of Human Genetics|August 23, 2016
Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset EncephalopathyEstelle Colin, Jens Daniel, Alban Ziegler, et al.
European Journal of Human Genetics : EJHG|May 16, 2022
Recommendations for whole genome sequencing in diagnostics for rare diseasesErika Souche, Sergi Beltran, Erwin Brosens, et al.
Epilepsia|December 6, 2024
Vigabatrin-associated brain magnetic resonance imaging abnormalities and clinical symptoms in infants with tuberous sclerosis complexCarmen Stevering, Maarten Lequin, Kinga Szczepaniak, et al.
Pageof 31

Showing results (281-290 of 310) with videos related to

Sort By:
Pageof 31
Epilepsia|April 3, 2016
Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in FranceMathilde Chipaux, William Szurhaj, Laurent Vercueil, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 27, 2018
Renal angiomyolipoma in patients with tuberous sclerosis complex: findings from the TuberOus SClerosis registry to increase disease AwarenessJ Chris Kingswood, Elena Belousova, Mirjana P Benedik, et al.
Epilepsia|January 27, 2024
Which terms should be used to describe medications used in the treatment of seizure disorders? An ILAE position paperEmilio Perucca, Jacqueline A French, Ghaieb Aljandeel, et al.
Frontiers in Neurology|April 9, 2021
TuberOus SClerosis registry to increAse disease awareness (TOSCA) Post-Authorisation Safety Study of Everolimus in Patients With Tuberous Sclerosis ComplexJ Chris Kingswood, Elena Belousova, Mirjana P Benedik, et al.
Frontiers in Neurology|September 28, 2020
Burden of Illness and Quality of Life in Tuberous Sclerosis Complex: Findings From the TOSCA StudyAnna C Jansen, Stephanie Vanclooster, Petrus J de Vries, et al.
Orphanet Journal of Rare Diseases|March 12, 2025
Gynecological issues in children and adolescents seen at rare-disease referral centers: an observational retrospective cohort studyIphigénie Cavadias, Magali Viaud, Marie Falampin, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Genetics of epilepsy: epilepsy research foundation workshop reportSanjay Sisodiya, J Helen Cross, Ingmar Blümcke, et al.
American Journal of Human Genetics|August 23, 2016
Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset EncephalopathyEstelle Colin, Jens Daniel, Alban Ziegler, et al.
European Journal of Human Genetics : EJHG|May 16, 2022
Recommendations for whole genome sequencing in diagnostics for rare diseasesErika Souche, Sergi Beltran, Erwin Brosens, et al.
Epilepsia|December 6, 2024
Vigabatrin-associated brain magnetic resonance imaging abnormalities and clinical symptoms in infants with tuberous sclerosis complexCarmen Stevering, Maarten Lequin, Kinga Szczepaniak, et al.
Pageof 31