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Maria T Acosta

Showing results (61-70 of 79) with videos related to

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Innovations in Clinical Neuroscience|March 18, 2024
Ensuring Stakeholder Feedback in the Design and Conduct of Clinical Trials for Rare Diseases: ISCTM Position Paper of the Orphan Disease Working GroupGahan J Pandina, Joan Busner, Lucas Kempf, et al.
Acta Neuropathologica|November 16, 2011
Neurofibromatosis 2011: a report of the Children's Tumor Foundation annual meetingMichel Kalamarides, Maria T Acosta, Dusica Babovic-Vuksanovic, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|April 5, 2024
Methods for Neuroscience Drug Development: Guidance on Standardization of the Process for Defining Clinical Outcome Strategies in Clinical TrialsSilvia Zaragoza Domingo, Jordi Alonso, Montse Ferrer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2025
Genome Sequencing Uncovers Additional Findings in Phelan-McDermid SyndromeRachel Gore Moses, Morgan Similuk, Alexandra Hehn, et al.
Molecular Genetics and Metabolism|January 29, 2023
Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patientsElena-Raluca Nicoli, Mylene Huebecker, Sangwoo T Han, et al.
Orphanet Journal of Rare Diseases|October 18, 2025
Methodological challenges in outcomes research for early-trials for implementation of new therapies in neuropediatric rare diseasesMaria T Acosta, Silvia Zaragoza Domingo, Celso Arango, et al.
NPJ Genomic Medicine|February 10, 2023
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairmentMarie Morimoto, Vikas Bhambhani, Nour Gazzaz, et al.
Journal of Attention Disorders|December 17, 2019
Cognition, ADHD Symptoms, and Functional Impairment in Children and Adolescents With Neurofibromatosis Type 1Jonathan M Payne, Kristina M Haebich, Rachel MacKenzie, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Back to the future: proceedings from the 2010 NF ConferenceSusan M Huson, Maria T Acosta, Allan J Belzberg, et al.
American Journal of Medical Genetics. Part A|December 4, 2024
Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network StudyQueenie K-G Tan, Allyn McConkie-Rosell, Rachel Mahoney, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Innovations in Clinical Neuroscience|March 18, 2024
Ensuring Stakeholder Feedback in the Design and Conduct of Clinical Trials for Rare Diseases: ISCTM Position Paper of the Orphan Disease Working GroupGahan J Pandina, Joan Busner, Lucas Kempf, et al.
Acta Neuropathologica|November 16, 2011
Neurofibromatosis 2011: a report of the Children's Tumor Foundation annual meetingMichel Kalamarides, Maria T Acosta, Dusica Babovic-Vuksanovic, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|April 5, 2024
Methods for Neuroscience Drug Development: Guidance on Standardization of the Process for Defining Clinical Outcome Strategies in Clinical TrialsSilvia Zaragoza Domingo, Jordi Alonso, Montse Ferrer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 16, 2025
Genome Sequencing Uncovers Additional Findings in Phelan-McDermid SyndromeRachel Gore Moses, Morgan Similuk, Alexandra Hehn, et al.
Molecular Genetics and Metabolism|January 29, 2023
Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patientsElena-Raluca Nicoli, Mylene Huebecker, Sangwoo T Han, et al.
Orphanet Journal of Rare Diseases|October 18, 2025
Methodological challenges in outcomes research for early-trials for implementation of new therapies in neuropediatric rare diseasesMaria T Acosta, Silvia Zaragoza Domingo, Celso Arango, et al.
NPJ Genomic Medicine|February 10, 2023
Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairmentMarie Morimoto, Vikas Bhambhani, Nour Gazzaz, et al.
Journal of Attention Disorders|December 17, 2019
Cognition, ADHD Symptoms, and Functional Impairment in Children and Adolescents With Neurofibromatosis Type 1Jonathan M Payne, Kristina M Haebich, Rachel MacKenzie, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Back to the future: proceedings from the 2010 NF ConferenceSusan M Huson, Maria T Acosta, Allan J Belzberg, et al.
American Journal of Medical Genetics. Part A|December 4, 2024
Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network StudyQueenie K-G Tan, Allyn McConkie-Rosell, Rachel Mahoney, et al.
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