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Diana Barca

Showing results (1-10 of 15) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|July 20, 2017
Practical clues for diagnosing WWOX encephalopathyOana Tarta-Arsene, Diana Barca, Dana Craiu, et al.
Maedica|October 7, 2011
Cohen syndrome - a rare genetic cause of hypotonia in childrenMagdalena Budisteanu, Diana Barca, Sorina Mihaela Chirieac, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 13, 2020
Testing blood and CSF in people with epilepsy: a practical guideFiona Sutton, Diana Barca, Ilia Komoltsev, et al.
Maedica|February 24, 2015
Intellectual disability and epilepsy in down syndromeDiana Barca, Oana Tarta-Arsene, Alice Dica, et al.
Journal of Biomedical Materials Research. Part B, Applied Biomaterials|August 7, 2010
Effect of silica coating combined to a MDP-based primer on the resin bond to Y-TZP ceramicLiliana Gressler May, Sheila Pestana Passos, Diana Barca Capelli, et al.
Maedica|May 3, 2014
Diagnostic approach of angelman syndromeDenis George Duca, Dana Craiu, Monica Boer, et al.
Molecular Genetics & Genomic Medicine|December 15, 2018
Clinical implementation of gene panel testing for lysosomal storage diseasesAlexander Gheldof, Sara Seneca, Katrien Stouffs, et al.
Experimental and Therapeutic Medicine|January 3, 2022
Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from RomaniaMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.
The Lancet. Diabetes & Endocrinology|August 5, 2019
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trialStefan Groeneweg, Robin P Peeters, Carla Moran, et al.
Annals of Neurology|October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypesMaureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Epileptic Disorders : International Epilepsy Journal with Videotape|July 20, 2017
Practical clues for diagnosing WWOX encephalopathyOana Tarta-Arsene, Diana Barca, Dana Craiu, et al.
Maedica|October 7, 2011
Cohen syndrome - a rare genetic cause of hypotonia in childrenMagdalena Budisteanu, Diana Barca, Sorina Mihaela Chirieac, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 13, 2020
Testing blood and CSF in people with epilepsy: a practical guideFiona Sutton, Diana Barca, Ilia Komoltsev, et al.
Maedica|February 24, 2015
Intellectual disability and epilepsy in down syndromeDiana Barca, Oana Tarta-Arsene, Alice Dica, et al.
Journal of Biomedical Materials Research. Part B, Applied Biomaterials|August 7, 2010
Effect of silica coating combined to a MDP-based primer on the resin bond to Y-TZP ceramicLiliana Gressler May, Sheila Pestana Passos, Diana Barca Capelli, et al.
Maedica|May 3, 2014
Diagnostic approach of angelman syndromeDenis George Duca, Dana Craiu, Monica Boer, et al.
Molecular Genetics & Genomic Medicine|December 15, 2018
Clinical implementation of gene panel testing for lysosomal storage diseasesAlexander Gheldof, Sara Seneca, Katrien Stouffs, et al.
Experimental and Therapeutic Medicine|January 3, 2022
Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from RomaniaMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.
The Lancet. Diabetes & Endocrinology|August 5, 2019
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trialStefan Groeneweg, Robin P Peeters, Carla Moran, et al.
Annals of Neurology|October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypesMaureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.
Pageof 2