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A Ververi

Showing results (1-10 of 8) with videos related to

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Current Neuropharmacology|December 2, 2009
The serotonergic system: its role in pathogenesis and early developmental treatment of autismD I Zafeiriou, A Ververi, E Vargiami
Clinical Genetics|July 11, 2017
Phenotypic spectrum associated with de novo mutations in QRICH1 geneA Ververi, M Splitt, J C S Dean, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 17, 2025
Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta-analysisA Sotiriadis, E Demertzidou, A Ververi, et al.
Molecular Genetics and Metabolism|March 14, 2009
Tyrosine hydroxylase deficiency with severe clinical courseD I Zafeiriou, M A Willemsen, M M Verbeek, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 8, 2008
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutationD I Zafeiriou, F Lehmann-Horn, E Vargiami, et al.
Brain & Development|November 6, 2007
L-2-Hydroxyglutaric aciduria presenting with severe autistic featuresD I Zafeiriou, A Ververi, G S Salomons, et al.
Neuropediatrics|November 11, 2008
MR spectroscopy and serial magnetic resonance imaging in a patient with mitochondrial cystic leukoencephalopathy due to complex I deficiency and NDUFV1 mutations and mild clinical courseD I Zafeiriou, R J T Rodenburg, H Scheffer, et al.
American Journal of Medical Genetics. Part A|June 24, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical RecommendationsE Woods, N Holmes, A S Denommé-Pichon, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Neuropharmacology|December 2, 2009
The serotonergic system: its role in pathogenesis and early developmental treatment of autismD I Zafeiriou, A Ververi, E Vargiami
Clinical Genetics|July 11, 2017
Phenotypic spectrum associated with de novo mutations in QRICH1 geneA Ververi, M Splitt, J C S Dean, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 17, 2025
Incremental yield of exome sequencing over standard prenatal testing in structurally normal fetuses: systematic review and meta-analysisA Sotiriadis, E Demertzidou, A Ververi, et al.
Molecular Genetics and Metabolism|March 14, 2009
Tyrosine hydroxylase deficiency with severe clinical courseD I Zafeiriou, M A Willemsen, M M Verbeek, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 8, 2008
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutationD I Zafeiriou, F Lehmann-Horn, E Vargiami, et al.
Brain & Development|November 6, 2007
L-2-Hydroxyglutaric aciduria presenting with severe autistic featuresD I Zafeiriou, A Ververi, G S Salomons, et al.
Neuropediatrics|November 11, 2008
MR spectroscopy and serial magnetic resonance imaging in a patient with mitochondrial cystic leukoencephalopathy due to complex I deficiency and NDUFV1 mutations and mild clinical courseD I Zafeiriou, R J T Rodenburg, H Scheffer, et al.
American Journal of Medical Genetics. Part A|June 24, 2025
An International ASXL3 Natural History Study: Deep Phenotypic Analyses Including Detailed Reports of a Milder Phenotype, Novel Associations, and Clinical RecommendationsE Woods, N Holmes, A S Denommé-Pichon, et al.
Pageof 1