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Roser Pons

Showing results (31-40 of 90) with videos related to

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Pediatric Neurology|January 3, 2017
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome: Additional Clinical FeaturesEvanthia A Makrygianni, George K Papadimas, George Vartzelis, et al.
Pediatric Research|March 4, 2003
Neonatal blood carnitine concentrations: normative data by electrospray tandem mass spectometryDonald H Chace, Roser Pons, Claudia A Chiriboga, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
Levodopa-induced dyskinesias in tyrosine hydroxylase deficiencyRoser Pons, Dimitris Syrengelas, Sotiris Youroukos, et al.
Journal of the Neurological Sciences|October 12, 2018
Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPAMaria Tsipi, Myrto Poulou, Irene Fylaktou, et al.
Journal of the Neurological Sciences|July 6, 2014
Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern EuropeMarta Vila-Pueyo, Roser Pons, Miquel Raspall-Chaure, et al.
Muscle & Nerve|May 15, 2016
Single amino acid loss in the dystrophin protein associated with a mild clinical phenotypeRoser Pons, Kyriaki Kekou, Artemis Gkika, et al.
Experimental and Therapeutic Medicine|August 18, 2022
Pathophysiology of cognitive dysfunction and the role of combined brain/heart magnetic resonance imaging (Review)George Markousis-Mavrogenis, Flora Bacopoulou, Genovefa Kolovou, et al.
Acta Dermato-Venereologica|June 5, 2023
Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek ChildrenLamprini Nasi, Alexios Alexopoulos, Eleftheria Kokkinou, et al.
European Journal of Clinical Investigation|October 14, 2017
Oedema-fibrosis in Duchenne Muscular Dystrophy: Role of cardiovascular magnetic resonance imagingSophie Mavrogeni, Antigoni Papavasiliou, Katerina Giannakopoulou, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|March 6, 2020
<i>HLA-DRB1</i> allele impact on pediatric multiple sclerosis in a Hellenic cohortMaria Gontika, Charalampos Skarlis, Artemios Artemiadis, et al.
Pageof 9

Showing results (31-40 of 90) with videos related to

Sort By:
Pageof 9
Pediatric Neurology|January 3, 2017
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome: Additional Clinical FeaturesEvanthia A Makrygianni, George K Papadimas, George Vartzelis, et al.
Pediatric Research|March 4, 2003
Neonatal blood carnitine concentrations: normative data by electrospray tandem mass spectometryDonald H Chace, Roser Pons, Claudia A Chiriboga, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
Levodopa-induced dyskinesias in tyrosine hydroxylase deficiencyRoser Pons, Dimitris Syrengelas, Sotiris Youroukos, et al.
Journal of the Neurological Sciences|October 12, 2018
Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPAMaria Tsipi, Myrto Poulou, Irene Fylaktou, et al.
Journal of the Neurological Sciences|July 6, 2014
Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern EuropeMarta Vila-Pueyo, Roser Pons, Miquel Raspall-Chaure, et al.
Muscle & Nerve|May 15, 2016
Single amino acid loss in the dystrophin protein associated with a mild clinical phenotypeRoser Pons, Kyriaki Kekou, Artemis Gkika, et al.
Experimental and Therapeutic Medicine|August 18, 2022
Pathophysiology of cognitive dysfunction and the role of combined brain/heart magnetic resonance imaging (Review)George Markousis-Mavrogenis, Flora Bacopoulou, Genovefa Kolovou, et al.
Acta Dermato-Venereologica|June 5, 2023
Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek ChildrenLamprini Nasi, Alexios Alexopoulos, Eleftheria Kokkinou, et al.
European Journal of Clinical Investigation|October 14, 2017
Oedema-fibrosis in Duchenne Muscular Dystrophy: Role of cardiovascular magnetic resonance imagingSophie Mavrogeni, Antigoni Papavasiliou, Katerina Giannakopoulou, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|March 6, 2020
<i>HLA-DRB1</i> allele impact on pediatric multiple sclerosis in a Hellenic cohortMaria Gontika, Charalampos Skarlis, Artemios Artemiadis, et al.
Pageof 9