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T Reiter

Showing results (101-110 of 111) with videos related to

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JMIR Research Protocols|October 20, 2017
Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early UsesOluwaseun Jessica Ajayi, Ebony Jeannae Smith, Teeradache Viangteeravat, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|August 14, 2021
Infratentorial MRI Findings in Rasmussen Encephalitis Suggest Primary Cerebellar InvolvementJohannes T Reiter, Bastian David, Selma Enders, et al.
Molecular Autism|February 20, 2015
Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1Noelle D Germain, Pin-Fang Chen, Alex M Plocik, et al.
Epilepsia|February 8, 2014
A survey of seizures and current treatments in 15q duplication syndromeKerry D Conant, Brenda Finucane, Nicole Cleary, et al.
Epilepsia|March 4, 2024
Evidence for interictal blood-brain barrier dysfunction in people with epilepsyJohannes T Reiter, Freya Schulte, Tobias Bauer, et al.
Human Molecular Genetics|October 11, 2017
Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndromeNycole A Copping, Sarah G B Christian, Dylan J Ritter, et al.
Annals of Clinical and Translational Neurology|August 27, 2024
Interictal blood-brain barrier dysfunction in piriform cortex of people with epilepsyFreya Schulte, Johannes T Reiter, Tobias Bauer, et al.
Human Molecular Genetics|January 5, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
Human Molecular Genetics|February 16, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
JCI Insight|September 4, 2020
Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide productionHelen Chen, A Kaitlyn Victor, Jonathon Klein, et al.
Pageof 12

Showing results (101-110 of 111) with videos related to

Sort By:
Pageof 12
JMIR Research Protocols|October 20, 2017
Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early UsesOluwaseun Jessica Ajayi, Ebony Jeannae Smith, Teeradache Viangteeravat, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|August 14, 2021
Infratentorial MRI Findings in Rasmussen Encephalitis Suggest Primary Cerebellar InvolvementJohannes T Reiter, Bastian David, Selma Enders, et al.
Molecular Autism|February 20, 2015
Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1Noelle D Germain, Pin-Fang Chen, Alex M Plocik, et al.
Epilepsia|February 8, 2014
A survey of seizures and current treatments in 15q duplication syndromeKerry D Conant, Brenda Finucane, Nicole Cleary, et al.
Epilepsia|March 4, 2024
Evidence for interictal blood-brain barrier dysfunction in people with epilepsyJohannes T Reiter, Freya Schulte, Tobias Bauer, et al.
Human Molecular Genetics|October 11, 2017
Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndromeNycole A Copping, Sarah G B Christian, Dylan J Ritter, et al.
Annals of Clinical and Translational Neurology|August 27, 2024
Interictal blood-brain barrier dysfunction in piriform cortex of people with epilepsyFreya Schulte, Johannes T Reiter, Tobias Bauer, et al.
Human Molecular Genetics|January 5, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
Human Molecular Genetics|February 16, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
JCI Insight|September 4, 2020
Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide productionHelen Chen, A Kaitlyn Victor, Jonathon Klein, et al.
Pageof 12