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Alcy Torres

Showing results (31-40 of 39) with videos related to

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Epilepsia|January 5, 2023
Temporal trends in the cost and use of first-line treatments for infantile epileptic spasms syndromeIván Sánchez Fernández, Marta Amengual-Gual, Cristina Barcia Aguilar, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 11, 2013
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delayYu An, Sami S Amr, Alcy Torres, et al.
Epilepsy & Behavior : E&B|May 25, 2010
Adaptive phase I study of OROS methylphenidate treatment of attention deficit hyperactivity disorder with epilepsyJoseph Gonzalez-Heydrich, Jane Whitney, Deborah Waber, et al.
Cold Spring Harbor Molecular Case Studies|September 15, 2016
A novel de novo mutation in ATP1A3 and childhood-onset schizophreniaNiklas Smedemark-Margulies, Catherine A Brownstein, Sigella Vargas, et al.
Journal of Neurotrauma|February 13, 2026
Younger Age of First Exposure to American Football Is Associated with Worse Informant-Reported Clinical Outcomes in Older Age Brain DonorsSophia B Nosek, Stephanie Gonzalez Gil, Bobak Abdolmohammadi, et al.
Molecular Genetics and Metabolism Reports|June 21, 2018
<i>De novo ATP1A3</i> and compound heterozygous <i>NLRP3</i> mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndromeAlcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
Neurology|November 11, 2018
Safety, tolerability, and efficacy of fluoxetine as an antiviral for acute flaccid myelitisKevin Messacar, Stefan Sillau, Sarah E Hopkins, et al.
Archives of General Psychiatry|October 10, 2012
Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesityCarl Ernst, Christian R Marshall, Yiping Shen, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Epilepsia|January 5, 2023
Temporal trends in the cost and use of first-line treatments for infantile epileptic spasms syndromeIván Sánchez Fernández, Marta Amengual-Gual, Cristina Barcia Aguilar, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 11, 2013
SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delayYu An, Sami S Amr, Alcy Torres, et al.
Epilepsy & Behavior : E&B|May 25, 2010
Adaptive phase I study of OROS methylphenidate treatment of attention deficit hyperactivity disorder with epilepsyJoseph Gonzalez-Heydrich, Jane Whitney, Deborah Waber, et al.
Cold Spring Harbor Molecular Case Studies|September 15, 2016
A novel de novo mutation in ATP1A3 and childhood-onset schizophreniaNiklas Smedemark-Margulies, Catherine A Brownstein, Sigella Vargas, et al.
Journal of Neurotrauma|February 13, 2026
Younger Age of First Exposure to American Football Is Associated with Worse Informant-Reported Clinical Outcomes in Older Age Brain DonorsSophia B Nosek, Stephanie Gonzalez Gil, Bobak Abdolmohammadi, et al.
Molecular Genetics and Metabolism Reports|June 21, 2018
<i>De novo ATP1A3</i> and compound heterozygous <i>NLRP3</i> mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndromeAlcy Torres, Catherine A Brownstein, Sahil K Tembulkar, et al.
Neurology|November 11, 2018
Safety, tolerability, and efficacy of fluoxetine as an antiviral for acute flaccid myelitisKevin Messacar, Stefan Sillau, Sarah E Hopkins, et al.
Archives of General Psychiatry|October 10, 2012
Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesityCarl Ernst, Christian R Marshall, Yiping Shen, et al.
Nature Genetics|June 29, 2023
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresisAlan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, et al.
Pageof 4