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Ian C Forster

Showing results (51-60 of 58) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 22, 2023
Retinal Dysfunction in a Mouse Model of HCN1 Genetic EpilepsyDa Zhao, Paulo Pinares-Garcia, Chaseley E McKenzie, et al.
Frontiers in Pharmacology|September 6, 2017
Gabapentin Modulates HCN4 Channel Voltage-DependenceHan-Shen Tae, Kelly M Smith, A Marie Phillips, et al.
Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
Brain : a Journal of Neurology|April 30, 2019
Novel GABRA2 variants in epileptic encephalopathy and intellectual disability with seizuresSnezana Maljevic, Boris Keren, Ye Htet Aung, et al.
Journal of the American Society of Nephrology : JASN|June 7, 2015
Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile HypercalcemiaKarl P Schlingmann, Justyna Ruminska, Martin Kaufmann, et al.
Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
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Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 22, 2023
Retinal Dysfunction in a Mouse Model of HCN1 Genetic EpilepsyDa Zhao, Paulo Pinares-Garcia, Chaseley E McKenzie, et al.
Frontiers in Pharmacology|September 6, 2017
Gabapentin Modulates HCN4 Channel Voltage-DependenceHan-Shen Tae, Kelly M Smith, A Marie Phillips, et al.
Brain : a Journal of Neurology|April 6, 2021
Cation leak underlies neuronal excitability in an HCN1 developmental and epileptic encephalopathyLauren E Bleakley, Chaseley E McKenzie, Ming S Soh, et al.
Brain : a Journal of Neurology|April 30, 2019
Novel GABRA2 variants in epileptic encephalopathy and intellectual disability with seizuresSnezana Maljevic, Boris Keren, Ye Htet Aung, et al.
Journal of the American Society of Nephrology : JASN|June 7, 2015
Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile HypercalcemiaKarl P Schlingmann, Justyna Ruminska, Martin Kaufmann, et al.
Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.
Annals of Neurology|June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell ModelsClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disordersClara Houdayer, A Marie Phillips, Marie Chabbert, et al.
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