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Roser Pons

Showing results (41-50 of 90) with videos related to

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Cancer Research|June 27, 2019
Antitumor Effects of Anti-Semaphorin 4D Antibody Unravel a Novel Proinvasive Mechanism of Vascular-Targeting AgentsIratxe Zuazo-Gaztelu, Marta Pàez-Ribes, Patricia Carrasco, et al.
Journal of Neurology|June 5, 2016
A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findingsAlexandros A Polymeris, Alessandra Tessa, Katherine Anagnostopoulou, et al.
The Journal of Pediatrics|January 15, 2004
Mitochondrial DNA abnormalities and autistic spectrum disordersRoser Pons, Antoni L Andreu, Nicoletta Checcarelli, et al.
Medical Sciences (Basel, Switzerland)|April 24, 2026
Cognitive and Psychosocial Burden of Childhood Cancer Survivors in Greece: A Case-Control StudyKalliopi Mavrea, Katerina Katsibardi, Kleoniki Roka, et al.
Acta Dermato-Venereologica|September 13, 2019
Novel PLEC Variant Causes Mild Skin Fragility, Pyloric Atresia, Muscular Dystrophy and Urological ManifestationsManthoula Valari, Martha Theodoraki, Ierotheos Loukas, et al.
International Journal of Molecular Sciences|June 19, 2024
<i>SCN1A</i> Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable PresentationsDanai Veltra, Virginia Theodorou, Marina Katsalouli, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|April 26, 2022
Natalizumab therapy in patients with pediatric-onset multiple sclerosis in Greece: clinical and immunological insights of time-long administration and future directions-a single-center retrospective observational studyMaria Gontika, Charalampos Skarlis, Nikolaos Markoglou, et al.
Muscle & Nerve|June 10, 2024
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifierNikolaos M Marinakis, Maria Svingou, Giorgos-Konstantinos Papadimas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2010
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutationRoser Pons, Mercedes Serrano, Aida Ormazabal, et al.
Journal of Clinical Medicine|November 11, 2022
Cardiovascular Magnetic Resonance Imaging Patterns in Rare Cardiovascular DiseasesGeorge Markousis-Mavrogenis, Aikaterini Giannakopoulou, Antonios Belegrinos, et al.
Pageof 9

Showing results (41-50 of 90) with videos related to

Sort By:
Pageof 9
Cancer Research|June 27, 2019
Antitumor Effects of Anti-Semaphorin 4D Antibody Unravel a Novel Proinvasive Mechanism of Vascular-Targeting AgentsIratxe Zuazo-Gaztelu, Marta Pàez-Ribes, Patricia Carrasco, et al.
Journal of Neurology|June 5, 2016
A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findingsAlexandros A Polymeris, Alessandra Tessa, Katherine Anagnostopoulou, et al.
The Journal of Pediatrics|January 15, 2004
Mitochondrial DNA abnormalities and autistic spectrum disordersRoser Pons, Antoni L Andreu, Nicoletta Checcarelli, et al.
Medical Sciences (Basel, Switzerland)|April 24, 2026
Cognitive and Psychosocial Burden of Childhood Cancer Survivors in Greece: A Case-Control StudyKalliopi Mavrea, Katerina Katsibardi, Kleoniki Roka, et al.
Acta Dermato-Venereologica|September 13, 2019
Novel PLEC Variant Causes Mild Skin Fragility, Pyloric Atresia, Muscular Dystrophy and Urological ManifestationsManthoula Valari, Martha Theodoraki, Ierotheos Loukas, et al.
International Journal of Molecular Sciences|June 19, 2024
<i>SCN1A</i> Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable PresentationsDanai Veltra, Virginia Theodorou, Marina Katsalouli, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|April 26, 2022
Natalizumab therapy in patients with pediatric-onset multiple sclerosis in Greece: clinical and immunological insights of time-long administration and future directions-a single-center retrospective observational studyMaria Gontika, Charalampos Skarlis, Nikolaos Markoglou, et al.
Muscle & Nerve|June 10, 2024
Myotonia congenita in a Greek cohort: Genotype spectrum and impact of the CLCN1:c.501C > G variant as a genetic modifierNikolaos M Marinakis, Maria Svingou, Giorgos-Konstantinos Papadimas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2010
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutationRoser Pons, Mercedes Serrano, Aida Ormazabal, et al.
Journal of Clinical Medicine|November 11, 2022
Cardiovascular Magnetic Resonance Imaging Patterns in Rare Cardiovascular DiseasesGeorge Markousis-Mavrogenis, Aikaterini Giannakopoulou, Antonios Belegrinos, et al.
Pageof 9