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Epilepsia
|
September 19, 2014
Vagus nerve stimulation for drug-resistant epilepsy: a European long-term study up to 24 months in 347 children
Iren Orosz, David McCormick, Nelia Zamponi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 26, 2016
Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency
Efterpi Pavlidou, Vincenzo Salpietro, Rahul Phadke, et al.
Cancer Chemotherapy and Pharmacology
|
November 19, 2010
Preclinical pharmacokinetics, metabolism, and toxicity of azurin-p28 (NSC745104) a peptide inhibitor of p53 ubiquitination
Lee Jia, Gregory S Gorman, Lori U Coward, et al.
Journal of Endourology
|
January 12, 2010
Bovine serum albumin glutaraldehyde for completely sutureless laparoscopic heminephrectomy in a survival porcine model
Michael K Louie, Aldrin Joseph R Gamboa, Adam G Kaplan, et al.
Journal of Medical Genetics
|
May 24, 2018
Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses
Laura Addis, William Sproviero, Sanjeev V Thomas, et al.
Journal of Veterinary Internal Medicine
|
December 26, 2006
Myeloma-related disorders in cats commonly present as extramedullary neoplasms in contrast to myeloma in human patients: 24 cases with clinical follow-up
Paul J Mellor, Sean Haugland, Sue Murphy, et al.
Annals of Clinical and Translational Neurology
|
July 8, 2016
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy
Naim Panjwani, Michael D Wilson, Laura Addis, et al.
Epilepsy & Behavior : E&B
|
November 19, 2015
Risk factors for reading disability in families with rolandic epilepsy
Yaiza Hernández Vega, Anna Smith, Hannah Cockerill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 10, 2023
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
Lauren Jeffries, Emily K Mis, Kirsty McWalter, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Epilepsia
|
September 19, 2014
Vagus nerve stimulation for drug-resistant epilepsy: a European long-term study up to 24 months in 347 children
Iren Orosz, David McCormick, Nelia Zamponi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 26, 2016
Pontocerebellar hypoplasia type 2D and optic nerve atrophy further expand the spectrum associated with selenoprotein biosynthesis deficiency
Efterpi Pavlidou, Vincenzo Salpietro, Rahul Phadke, et al.
Cancer Chemotherapy and Pharmacology
|
November 19, 2010
Preclinical pharmacokinetics, metabolism, and toxicity of azurin-p28 (NSC745104) a peptide inhibitor of p53 ubiquitination
Lee Jia, Gregory S Gorman, Lori U Coward, et al.
Journal of Endourology
|
January 12, 2010
Bovine serum albumin glutaraldehyde for completely sutureless laparoscopic heminephrectomy in a survival porcine model
Michael K Louie, Aldrin Joseph R Gamboa, Adam G Kaplan, et al.
Journal of Medical Genetics
|
May 24, 2018
Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses
Laura Addis, William Sproviero, Sanjeev V Thomas, et al.
Journal of Veterinary Internal Medicine
|
December 26, 2006
Myeloma-related disorders in cats commonly present as extramedullary neoplasms in contrast to myeloma in human patients: 24 cases with clinical follow-up
Paul J Mellor, Sean Haugland, Sue Murphy, et al.
Annals of Clinical and Translational Neurology
|
July 8, 2016
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy
Naim Panjwani, Michael D Wilson, Laura Addis, et al.
Epilepsy & Behavior : E&B
|
November 19, 2015
Risk factors for reading disability in families with rolandic epilepsy
Yaiza Hernández Vega, Anna Smith, Hannah Cockerill, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 10, 2023
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
Lauren Jeffries, Emily K Mis, Kirsty McWalter, et al.
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