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Kaindl

Showing results (401-410 of 543) with videos related to

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Frontiers in Neurology|November 7, 2022
Case report: Expanding the phenotype of <i>ARHGEF17</i> mutations from increased intracranial aneurysm risk to a neurodevelopmental diseaseEthiraj Ravindran, Noor Ullah, Shyamala Mani, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2022
Ictal EEG recording is not mandatory in all candidates for paediatric epilepsy surgery with clear MRI lesions and corresponding seizure semiologyKonstantin L Makridis, Christine Prager, Deniz A Atalay, et al.
Developmental Cognitive Neuroscience|December 25, 2022
Distinct multivariate structural brain profiles are related to variations in short- and long-delay memory consolidation across children and young adultsIryna Schommartz, Philip F Lembcke, Francesco Pupillo, et al.
Journal of Neuropathology and Experimental Neurology|January 6, 2007
Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathiesMuriel Herasse, Karine Parain, Isabelle Marty, et al.
Cell Reports|February 20, 2026
In utero exposure to NMDA receptor autoantibodies disrupts hippocampal circuit maturationMyrtill Majoros, Chuanqiang Zhang, Vahid Rahmati, et al.
Molecular Cell|May 20, 2019
Conformational Complexity and Dynamics in a Muscarinic Receptor Revealed by NMR SpectroscopyJun Xu, Yunfei Hu, Jonas Kaindl, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 15, 2017
Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephalyAnsar A Abbasi, Kathrin Blaesius, Hao Hu, et al.
HGG Advances|October 10, 2024
Togaram1 is expressed in the neural tube and its absence causes neural tube closure defectsYanyan Wang, Nadine Kraemer, Joanna Schneider, et al.
Orphanet Journal of Rare Diseases|May 1, 2016
Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPDSylvie Picker-Minh, Cyril Mignot, Diane Doummar, et al.
Developmental Medicine and Child Neurology|March 13, 2014
Diagnostic approach to microcephaly in childhood: a two-center study and review of the literatureMaja von der Hagen, Mark Pivarcsi, Juliane Liebe, et al.
Pageof 55

Showing results (401-410 of 543) with videos related to

Sort By:
Pageof 55
Frontiers in Neurology|November 7, 2022
Case report: Expanding the phenotype of <i>ARHGEF17</i> mutations from increased intracranial aneurysm risk to a neurodevelopmental diseaseEthiraj Ravindran, Noor Ullah, Shyamala Mani, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2022
Ictal EEG recording is not mandatory in all candidates for paediatric epilepsy surgery with clear MRI lesions and corresponding seizure semiologyKonstantin L Makridis, Christine Prager, Deniz A Atalay, et al.
Developmental Cognitive Neuroscience|December 25, 2022
Distinct multivariate structural brain profiles are related to variations in short- and long-delay memory consolidation across children and young adultsIryna Schommartz, Philip F Lembcke, Francesco Pupillo, et al.
Journal of Neuropathology and Experimental Neurology|January 6, 2007
Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathiesMuriel Herasse, Karine Parain, Isabelle Marty, et al.
Cell Reports|February 20, 2026
In utero exposure to NMDA receptor autoantibodies disrupts hippocampal circuit maturationMyrtill Majoros, Chuanqiang Zhang, Vahid Rahmati, et al.
Molecular Cell|May 20, 2019
Conformational Complexity and Dynamics in a Muscarinic Receptor Revealed by NMR SpectroscopyJun Xu, Yunfei Hu, Jonas Kaindl, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 15, 2017
Identification of a novel homozygous TRAPPC9 gene mutation causing non-syndromic intellectual disability, speech disorder, and secondary microcephalyAnsar A Abbasi, Kathrin Blaesius, Hao Hu, et al.
HGG Advances|October 10, 2024
Togaram1 is expressed in the neural tube and its absence causes neural tube closure defectsYanyan Wang, Nadine Kraemer, Joanna Schneider, et al.
Orphanet Journal of Rare Diseases|May 1, 2016
Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPDSylvie Picker-Minh, Cyril Mignot, Diane Doummar, et al.
Developmental Medicine and Child Neurology|March 13, 2014
Diagnostic approach to microcephaly in childhood: a two-center study and review of the literatureMaja von der Hagen, Mark Pivarcsi, Juliane Liebe, et al.
Pageof 55