关注
Nahla M. Alshaikh
Nahla M. Alshaikh
King Saud bin Abdulaziz University for Health Sciences
在 ngha.med.sa 的电子邮件经过验证
标题
引用次数
引用次数
年份
MRI in sarcoglycanopathies: a large international cohort study
G Tasca, M Monforte, J Díaz-Manera, G Brisca, C Semplicini, A D’Amico, ...
Journal of Neurology, Neurosurgery & Psychiatry 89 (1), 72-77, 2018
712018
Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability
AM Bertoli-Avella, JM Garcia-Aznar, O Brandau, F Al-Hakami, Z Yüksel, ...
European Journal of Human Genetics 26 (4), 592-598, 2018
262018
Perception of pain during electromyography in children: A prospective study
NM Alshaikh, JP Martinez, MC Pitt
Muscle & Nerve 54 (3), 422-426, 2016
252016
Vitamin D in corticosteroid-naïve and corticosteroid-treated Duchenne muscular dystrophy: what dose achieves optimal 25 (OH) vitamin D levels?
N Alshaikh, A Brunklaus, T Davis, SA Robb, R Quinlivan, P Munot, ...
Archives of Disease in Childhood 101 (10), 957-961, 2016
172016
Consensus statement on the management of duchenne muscular dystrophy in Saudi Arabia during the coronavirus disease 2019 pandemic
AK Bamaga, F Alghamdi, N Alshaikh, W Altwaijri, FA Bashiri, K Hundallah, ...
Frontiers in pediatrics 9, 629549, 2021
142021
Type III spinal muscular atrophy mimicking muscular dystrophies
AS Alsaman, NM AlShaikh
Pediatric Neurology 48 (5), 363-366, 2013
122013
Hepatic encephalopathy coexists with acquired chronic hepatocerebral degeneration
FZ Huang, X Hou, TQ Zhou, S Chen
Neurosciences Journal 20 (3), 277-279, 2015
112015
A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19
F Alghamdi, N Alshaikh, AK Bamaga, FA Bashiri, K Hundullah, A Alshehri, ...
Neurosciences Journal 25 (3), 230-237, 2020
42020
Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia
AS AlSaman, F Al Ghamdi, AK Bamaga, N AlShaikh, M Al Muqbil, ...
Frontiers in Pediatrics 10, 1020059, 2022
32022
Bridging the Gap: Parents’ Knowledge of Childhood Developmental Milestones and the Early Identification of Children With Developmental Delay
HM Alghamdi, BA Altirkistani, RA Baatya, YO Marghalani, NM Alshaikh
Cureus 15 (11), 2023
12023
Clinical and molecular characteristics of tectonic (TCTN1) gene-related Joubert syndrome in a Saudi boy
BH Shirah, NM Alshaikh, A Shawli, MI Naseer
Brain and Development 44 (4), 299-302, 2022
2022
Erratum: A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19.
F Alghamdi, N Alshaikh, AK Bamaga, FA Bashiri, K Hundallah, A Alshehri, ...
Neurosciences (Riyadh, Saudi Arabia) 25 (5), 440-440, 2020
2020
Validation of gene causality for neurological disorders by WES/WGS analyses in a diagnostic setting
AM Avella, Z Yueksel, H Yavuz, C Baldi, A Marais, JM Garcia-Aznar, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 524-526, 2019
2019
BALANCING PLACEBO AND NOCEBO EFFECTS DURING ELECTROMYOGRAPHY IN CHILDREN REPLY
NM Alshaikh, JP Martinez, MC Pitt
MUSCLE & NERVE 54 (4), 812-812, 2016
2016
Editor's Choice Articles
TM Jenkins, JJP Alix, RH Kandler, PJ Shaw, CJ McDermott, NM Alshaikh, ...
Perception, 2016
2016
Vitamin D in corticosteroid treated Duchenne muscular dystrophy: What dose achieves serum 25OH vitamin D sufficiency?
N Alshaikh, A Brunklaus, T Davis, S Robb, R Quinlivan, P Munot, ...
Neuromuscular Disorders 25, S302, 2015
2015
Clinical outcomes in a large cohort of boys and adolescents with Duchenne muscular dystrophy
N Alshaikh, A Brunklaus, S Robb, R Quinlivan, P Munot, A Sarkozy, ...
Neuromuscular Disorders 25, S302-S303, 2015
2015
系统目前无法执行此操作,请稍后再试。
文章 1–17