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Catrinel Iliescu

Showing results (11-20 of 17) with videos related to

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Genes|August 6, 2021
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 PatientsMagdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata, et al.
Genes|August 28, 2025
<i>FMR1</i> Methylation Pattern and Repeat Expansion Screening in a Cohort of Boys with Autism Spectrum Disorders: Correlation of Genetic Findings with Clinical PresentationsMaria Dobre, Gisela Gaina, Alina Erbescu, et al.
Diseases (Basel, Switzerland)|July 25, 2025
Age-Onset-Related Particularities of Pediatric MS-Understanding the Spectrum: A Tertiary Center ExperienceAlice Denisa Dică, Dana Craiu, Florentina Ionela Linca, et al.
Epilepsia|September 2, 2021
Exploring the prevalence and profile of epilepsy across Europe using a standard retrospective chart review: Challenges and opportunitiesChristine Linehan, Ailbhe Benson, Alex Gunko, et al.
Neuropediatrics|October 20, 2015
A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing PanencephalitisMartin Häusler, Ayse Aksoy, Michael Alber, et al.
European Journal of Human Genetics : EJHG|June 30, 2016
Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsyGabrielle Rudolf, Gaetan Lesca, Mana M Mehrjouy, et al.
Epilepsia|July 2, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variantsClaudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Genes|August 6, 2021
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 PatientsMagdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata, et al.
Genes|August 28, 2025
<i>FMR1</i> Methylation Pattern and Repeat Expansion Screening in a Cohort of Boys with Autism Spectrum Disorders: Correlation of Genetic Findings with Clinical PresentationsMaria Dobre, Gisela Gaina, Alina Erbescu, et al.
Diseases (Basel, Switzerland)|July 25, 2025
Age-Onset-Related Particularities of Pediatric MS-Understanding the Spectrum: A Tertiary Center ExperienceAlice Denisa Dică, Dana Craiu, Florentina Ionela Linca, et al.
Epilepsia|September 2, 2021
Exploring the prevalence and profile of epilepsy across Europe using a standard retrospective chart review: Challenges and opportunitiesChristine Linehan, Ailbhe Benson, Alex Gunko, et al.
Neuropediatrics|October 20, 2015
A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing PanencephalitisMartin Häusler, Ayse Aksoy, Michael Alber, et al.
European Journal of Human Genetics : EJHG|June 30, 2016
Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsyGabrielle Rudolf, Gaetan Lesca, Mana M Mehrjouy, et al.
Epilepsia|July 2, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variantsClaudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga, et al.
Pageof 2