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Brain Research
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March 11, 2009
Differential interaction of the Pafah1b alpha subunits with the Reelin transducer Dab1
Guangcheng Zhang, Amir H Assadi, Mila Roceri, et al.
Neuroscience Letters
|
June 3, 2008
Pafah1b2 mutations suppress the development of hydrocephalus in compound Pafah1b1; Reln and Pafah1b1; Dab1 mutant mice
Amir H Assadi, Guangcheng Zhang, Robert McNeil, et al.
The Clinical Neuropsychologist
|
January 31, 2019
Case report of prenatal bilateral cerebellar infarction: implications for social-behavioral functioning
Sara E Whiting, Audrey M Carson, Gary D Clark, et al.
Journal of Child Neurology
|
January 27, 2011
Bilateral in utero cerebellar infarction
Safdar A Ansari, Jill V Hunter, Lisa M Nassif, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 31, 2003
Previously uncharacterized roles of platelet-activating factor acetylhydrolase 1b complex in mouse spermatogenesis
Wei Yan, Amir H Assadi, Anthony Wynshaw-Boris, et al.
American Journal of Medical Genetics. Part A
|
June 4, 2011
Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2
Melissa B Ramocki, Fernando Scaglia, Pawel Stankiewicz, et al.
Plos One
|
March 3, 2007
The Pafah1b complex interacts with the reelin receptor VLDLR
Guangcheng Zhang, Amir H Assadi, Robert S McNeil, et al.
Epilepsia Open
|
August 1, 2024
Long-term efficacy and safety of cannabidiol in patients with tuberous sclerosis complex: 3-year results from the cannabidiol expanded access program
Arie Weinstock, E Martina Bebin, Daniel Checketts, et al.
Pediatrics
|
November 3, 2004
Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas
Stephen M Maricich, Jeffrey L Neul, Timothy E Lotze, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria
David R Murdock, Gary D Clark, Matthew N Bainbridge, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Brain Research
|
March 11, 2009
Differential interaction of the Pafah1b alpha subunits with the Reelin transducer Dab1
Guangcheng Zhang, Amir H Assadi, Mila Roceri, et al.
Neuroscience Letters
|
June 3, 2008
Pafah1b2 mutations suppress the development of hydrocephalus in compound Pafah1b1; Reln and Pafah1b1; Dab1 mutant mice
Amir H Assadi, Guangcheng Zhang, Robert McNeil, et al.
The Clinical Neuropsychologist
|
January 31, 2019
Case report of prenatal bilateral cerebellar infarction: implications for social-behavioral functioning
Sara E Whiting, Audrey M Carson, Gary D Clark, et al.
Journal of Child Neurology
|
January 27, 2011
Bilateral in utero cerebellar infarction
Safdar A Ansari, Jill V Hunter, Lisa M Nassif, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 31, 2003
Previously uncharacterized roles of platelet-activating factor acetylhydrolase 1b complex in mouse spermatogenesis
Wei Yan, Amir H Assadi, Anthony Wynshaw-Boris, et al.
American Journal of Medical Genetics. Part A
|
June 4, 2011
Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2
Melissa B Ramocki, Fernando Scaglia, Pawel Stankiewicz, et al.
Plos One
|
March 3, 2007
The Pafah1b complex interacts with the reelin receptor VLDLR
Guangcheng Zhang, Amir H Assadi, Robert S McNeil, et al.
Epilepsia Open
|
August 1, 2024
Long-term efficacy and safety of cannabidiol in patients with tuberous sclerosis complex: 3-year results from the cannabidiol expanded access program
Arie Weinstock, E Martina Bebin, Daniel Checketts, et al.
Pediatrics
|
November 3, 2004
Neurologic complications associated with influenza A in children during the 2003-2004 influenza season in Houston, Texas
Stephen M Maricich, Jeffrey L Neul, Timothy E Lotze, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria
David R Murdock, Gary D Clark, Matthew N Bainbridge, et al.
Page
of 3