دنبال کردن
Sophie Hill
Sophie Hill
Postdoctoral Fellow, Children's Hospital of Philadelphia
ایمیل تأیید شده در chop.edu
عنوان
نقل شده توسط
نقل شده توسط
سال
How to GRADE the quality of the evidence
R Ryan, S Hill
Cochrane consumers and communication group 3, 2016
4982016
Sodium channelopathies in neurodevelopmental disorders
MH Meisler, SF Hill, W Yu
Nature Reviews Neuroscience 22 (3), 152-166, 2021
1382021
Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome
GM Lenk, P Jafar‐Nejad, SF Hill, LD Huffman, CE Smolen, JL Wagnon, ...
Annals of neurology 87 (3), 339-346, 2020
1292020
The role of patient satisfaction surveys in a national approach to hospital quality management
M Draper, S Hill
AGPS, 1995
921995
Antisense oligonucleotide therapy for neurodevelopmental disorders
SF Hill, MH Meisler
Developmental neuroscience 43 (3-4), 247-252, 2021
832021
How to GRADE the quality of the evidence. Cochrane Consumers and Communication Group. 2016
R Ryan, S Hill
602019
How to GRADE the quality of the evidence. Cochrane Consumers and Communication Group, Version 3.0. 2016
R Ryan, S Hill
372019
CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development
H Yao, SF Hill, JM Skidmore, ED Sperry, DL Swiderski, GJ Sanchez, ...
JCI insight 3 (4), e97440, 2018
352018
CHD7 promotes neural progenitor differentiation in embryonic stem cells via altered chromatin accessibility and nascent gene expression
H Yao, DF Hannum, Y Zhai, SF Hill, RDO Albanus, W Lou, JM Skidmore, ...
Scientific reports 10 (1), 17445, 2020
322020
How to GRADE the quality of the evidence. 2016
R Ryan, S Hill
cccrg. cochrane. org/author‐resources, 2020
292020
How to GRADE the quality of the evidence. Cochrane Consumers and Communication Group. Version 3.0
R Ryan, S Hill
cccrg. cochrane. org/author-resources, 2016
252016
Gabra2 is a genetic modifier of Scn8a encephalopathy in the mouse
W Yu, SF Hill, JG Xenakis, F Pardo‐Manuel de Villena, JL Wagnon, ...
Epilepsia 61 (12), 2847-2856, 2020
192020
Genetic interaction between Scn8a and potassium channel genes Kcna1 and Kcnq2
SF Hill, JM Ziobro, P Jafar‐Nejad, F Rigo, MH Meisler
Epilepsia 63 (10), e125-e131, 2022
132022
How to GRADE the quality of the evidence. Version 3.0. December 2016
R Ryan, S Hill
Cochrane Consumers and Communication Group, available at cccrg. cochrane …, 2016
122016
Cochrane Consumers and Communication Group. How to GRADE the quality of the evidence
R Ryan, S Hill
112018
Spontaneous seizures and elevated seizure susceptibility in response to somatic mutation of sodium channel Scn8a in the mouse
W Yu, CE Smolen, SF Hill, MH Meisler
Human Molecular Genetics 30 (10), 902-907, 2021
72021
Reduction of Kcnt1 is therapeutic in mouse models of SCN1A and SCN8A epilepsy
SF Hill, P Jafar-Nejad, F Rigo, MH Meisler
Frontiers in Neuroscience 17, 1282201, 2023
52023
Long‐Term Downregulation of the Sodium Channel Gene Scn8a Is Therapeutic in Mouse Models of SCN8A Epilepsy
SF Hill*, W Yu*, J Ziobro, S Chalasani, F Reger, MH Meisler
Annals of Neurology 95 (4), 754-759, 2024
42024
Going virtual: Successes and shortcomings of a synchronous STEM outreach event
P Prizlow, M Quirk, KJ Schache, S Bhakkad, EC Laub, EL Xu, S Hill
Journal of Chemical Education 99 (5), 1990-1997, 2022
42022
Allele‐Specific Editing of a Dominant SCN8A Epilepsy Variant Protects against Seizures and Lethality in a Murine Model
W Yu, SF Hill, Y Huang, L Zhu, Y Demetriou, J Ziobro, F Reger, X Jia, ...
Annals of Neurology 96 (5), 958-969, 2024
12024
سیستم در حال حاضر قادر به انجام عملکرد نیست. بعداً دوباره امتحان کنید.
مقاله‌ها 1–20