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Sara Seneca

Showing results (11-20 of 88) with videos related to

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Ophthalmic Genetics|November 12, 2010
Ptosis as an associated finding in maternally inherited diabetes and deafnessKirsten Robberecht, Christian Decock, Annemie Stevens, et al.
Biomed Research International|March 1, 2016
Sertoli Cell-Only Syndrome: Behind the Genetic ScenesKatrien Stouffs, Alexander Gheldof, Herman Tournaye, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 8, 2012
DGUOK-related mitochondrial DNA depletion syndrome in a child with an early diagnosis of glycogen storage diseaseCiğdem S Kasapkara, Leyla Tümer, Aynur Küçükçongar, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Bioinformatics (Oxford, England)|December 1, 2022
EDIR: exome database of interspersed repeatsLaura D T Vo Ngoc, Randy Osei, Katrin Dohr, et al.
Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 3, 2008
Unusual findings in Leigh syndrome caused by T8993C mutationUluç Yiş, Sara Seneca, Eray Dirik, et al.
Human Mutation|June 21, 2007
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) regionWilly Lissens, Alessia Arena, Sara Seneca, et al.
Forensic Science International. Genetics|October 31, 2025
The first population scale compendium of complete mitochondrial genomes from Flanders, BelgiumNoah Gaens, Erika Souche, Toomas Kivisild, et al.
Journal of Assisted Reproduction and Genetics|May 19, 2015
Ovarian hyperstimulation syndrome after gonadotropin-releasing hormone agonist triggering and "freeze-all": in-depth analysis of genetic predispositionSamuel Santos-Ribeiro, Nikolaos P Polyzos, Katrien Stouffs, et al.
Pageof 9

Showing results (11-20 of 88) with videos related to

Sort By:
Pageof 9
Ophthalmic Genetics|November 12, 2010
Ptosis as an associated finding in maternally inherited diabetes and deafnessKirsten Robberecht, Christian Decock, Annemie Stevens, et al.
Biomed Research International|March 1, 2016
Sertoli Cell-Only Syndrome: Behind the Genetic ScenesKatrien Stouffs, Alexander Gheldof, Herman Tournaye, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 8, 2012
DGUOK-related mitochondrial DNA depletion syndrome in a child with an early diagnosis of glycogen storage diseaseCiğdem S Kasapkara, Leyla Tümer, Aynur Küçükçongar, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Bioinformatics (Oxford, England)|December 1, 2022
EDIR: exome database of interspersed repeatsLaura D T Vo Ngoc, Randy Osei, Katrin Dohr, et al.
Acta Neurologica Belgica|December 13, 2007
The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disordersAnn Meulemans, Erik Gerlo, Sara Seneca, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 3, 2008
Unusual findings in Leigh syndrome caused by T8993C mutationUluç Yiş, Sara Seneca, Eray Dirik, et al.
Human Mutation|June 21, 2007
A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) regionWilly Lissens, Alessia Arena, Sara Seneca, et al.
Forensic Science International. Genetics|October 31, 2025
The first population scale compendium of complete mitochondrial genomes from Flanders, BelgiumNoah Gaens, Erika Souche, Toomas Kivisild, et al.
Journal of Assisted Reproduction and Genetics|May 19, 2015
Ovarian hyperstimulation syndrome after gonadotropin-releasing hormone agonist triggering and "freeze-all": in-depth analysis of genetic predispositionSamuel Santos-Ribeiro, Nikolaos P Polyzos, Katrien Stouffs, et al.
Pageof 9