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Diana Rodriguez

Showing results (121-130 of 193) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Agentic Generative Artificial Intelligence System for Classification of Pathology-Confirmed Primary Progressive Aphasia VariantsChiara Gallingani, Zachary A Miller, Maria Luisa Mandelli, et al.
Prenatal Diagnosis|January 2, 2024
Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow-upAlienor Jaillard, Stéphanie Valence, Saskia Vande Perre, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|November 30, 2021
Clinical utility of family history of depression for prognosis of adolescent depression severity and duration assessed with predictive modelingLisa S Gorham, Neda Sadeghi, Lillian Eisner, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 11, 2017
Deficit in phonological processes: a characteristic of the neuropsychological profile of children with NF1Yves Chaix, Valérie Lauwers-Cancès, Nathalie Faure-Marie, et al.
Brain : a Journal of Neurology|October 4, 2017
Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophyImen Dorboz, Chiara Aiello, Cas Simons, et al.
Brain : a Journal of Neurology|July 24, 2009
Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 casesPierre Labauge, Laetitia Horzinski, Xavier Ayrignac, et al.
Journal of Child Neurology|January 28, 2021
Reading Comprehension Impairment in Children With Neurofibromatosis Type 1 (NF1): The Need of Multimodal Assessment of AttentionMaëlle Biotteau, Elodie Tournay, Eloise Baudou, et al.
Epilepsia|June 9, 2025
Broadening the phenotype associated with pathogenic variants in the FGF12 gene: From developmental and epileptic encephalopathy to drug-responsive epilepsy with favorable cognitive outcomeClément Pierret, Florence Riccardi, Julien Neveu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 11, 2026
Rationalizing thrombophilia screening in children: Insights from a 2019 retrospective study at a tertiary care hospitalManon Leleu, Guillaume Nguyen, Hélène Boutroux, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 25, 2021
Antiphospholipase A2 receptor antibody-positive membranous nephropathy in the kidney donor: Lessons from a serendipitous transplantationAlicia Molina Andújar, Natalia Castrejon de Anta, Diana Rodriguez-Espinosa, et al.
Pageof 20

Showing results (121-130 of 193) with videos related to

Sort By:
Pageof 20
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Agentic Generative Artificial Intelligence System for Classification of Pathology-Confirmed Primary Progressive Aphasia VariantsChiara Gallingani, Zachary A Miller, Maria Luisa Mandelli, et al.
Prenatal Diagnosis|January 2, 2024
Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow-upAlienor Jaillard, Stéphanie Valence, Saskia Vande Perre, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|November 30, 2021
Clinical utility of family history of depression for prognosis of adolescent depression severity and duration assessed with predictive modelingLisa S Gorham, Neda Sadeghi, Lillian Eisner, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 11, 2017
Deficit in phonological processes: a characteristic of the neuropsychological profile of children with NF1Yves Chaix, Valérie Lauwers-Cancès, Nathalie Faure-Marie, et al.
Brain : a Journal of Neurology|October 4, 2017
Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophyImen Dorboz, Chiara Aiello, Cas Simons, et al.
Brain : a Journal of Neurology|July 24, 2009
Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 casesPierre Labauge, Laetitia Horzinski, Xavier Ayrignac, et al.
Journal of Child Neurology|January 28, 2021
Reading Comprehension Impairment in Children With Neurofibromatosis Type 1 (NF1): The Need of Multimodal Assessment of AttentionMaëlle Biotteau, Elodie Tournay, Eloise Baudou, et al.
Epilepsia|June 9, 2025
Broadening the phenotype associated with pathogenic variants in the FGF12 gene: From developmental and epileptic encephalopathy to drug-responsive epilepsy with favorable cognitive outcomeClément Pierret, Florence Riccardi, Julien Neveu, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 11, 2026
Rationalizing thrombophilia screening in children: Insights from a 2019 retrospective study at a tertiary care hospitalManon Leleu, Guillaume Nguyen, Hélène Boutroux, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 25, 2021
Antiphospholipase A2 receptor antibody-positive membranous nephropathy in the kidney donor: Lessons from a serendipitous transplantationAlicia Molina Andújar, Natalia Castrejon de Anta, Diana Rodriguez-Espinosa, et al.
Pageof 20