|Human C9ORF72 hexanucleotide expansion reproduces RNA foci and dipeptide repeat proteins but not neurodegeneration in BAC transgenic mice|
OM Peters, GT Cabrera, H Tran, TF Gendron, JE McKeon, J Metterville, ...
Neuron 88 (5), 902-909, 2015
|Partial loss of TDP-43 function causes phenotypes of amyotrophic lateral sclerosis|
C Yang, H Wang, T Qiao, B Yang, L Aliaga, L Qiu, W Tan, J Salameh, ...
Proceedings of the National Academy of Sciences 111 (12), E1121-E1129, 2014
|A randomized trial of mexiletine in ALS: safety and effects on muscle cramps and progression|
MD Weiss, EA Macklin, Z Simmons, AS Knox, DJ Greenblatt, N Atassi, ...
Neurology 86 (16), 1474-1481, 2016
|ALS‐linked protein disulfide isomerase variants cause motor dysfunction|
U Woehlbier, A Colombo, MJ Saaranen, V Pérez, J Ojeda, FJ Bustos, ...
The EMBO journal 35 (8), 845-865, 2016
|Adeno‐associated virus–delivered artificial microRNA extends survival and delays paralysis in an amyotrophic lateral sclerosis mouse model|
L Stoica, SH Todeasa, GT Cabrera, JS Salameh, MK ElMallah, C Mueller, ...
Annals of neurology 79 (4), 687-700, 2016
|Amyotrophic lateral sclerosis|
JS Salameh, RH Brown Jr, JD Berry
Seminars in neurology 35 (04), 469-476, 2015
|Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing|
TI Jones, C Yan, PC Sapp, D McKenna-Yasek, PB Kang, C Quinn, ...
Clinical epigenetics 6 (1), 1-16, 2014
|Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging|
F Tian, W Yang, DA Mordes, JY Wang, JS Salameh, J Mok, J Chew, ...
Nature communications 7 (1), 1-15, 2016
|Necrotizing myopathies: an update|
C Quinn, JS Salameh, T Smith, N Souayah
Journal of clinical neuromuscular disease 16 (3), 131-140, 2015
|Medical research productivity in the Arab countries: 2007-2016 bibliometric analysis|
R El Rassi, LI Meho, A Nahlawi, JS Salameh, A Bazarbachi, EA Akl
Journal of global health 8 (2), 2018
|Amyotrophic lateral sclerosis: analysis of ALS cases in a predominantly admixed population of Ecuador|
M Bucheli, A Andino, M Montalvo, J Cruz, N Atassi, J Berry, J Salameh
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 15 (1-2), 106-113, 2014
|Loss of Sarm1 does not suppress motor neuron degeneration in the SOD1G93A mouse model of amyotrophic lateral sclerosis|
OM Peters, EA Lewis, JM Osterloh, A Weiss, JS Salameh, J Metterville, ...
Human molecular genetics 27 (21), 3761-3771, 2018
E Malek, J Salameh
Seminars in neurology 39 (05), 589-595, 2019
|An open label study of a novel immunosuppression intervention for the treatment of amyotrophic lateral sclerosis|
CN Fournier, D Schoenfeld, JD Berry, ME Cudkowicz, J Chan, C Quinn, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 19 (3-4), 242-249, 2018
|Phosphoglycerate mutase deficiency with tubular aggregates in a patient from Panama|
J Salameh, N Goyal, R Choudry, S Camelo‐Piragua, PST Chong
Muscle & nerve 47 (1), 138-140, 2013
|SOD1 (A4V)‐mediated ALS presenting with lower motor neuron facial diplegia and unilateral vocal cord paralysis|
JS Salameh, N Atassi, WS David
Muscle & Nerve: Official Journal of the American Association of …, 2009
|A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1|
YB Liu, A Tewari, J Salameh, E Arystarkhova, TG Hampton, A Brashear, ...
Elife 4, e11102, 2015
|Impaired neurodevelopment by the low complexity domain of CPEB4 reveals a convergent pathway with neurodegeneration|
J Shin, JS Salameh, JD Richter
Scientific reports 6 (1), 1-14, 2016
|A 62-year-old woman with cerebral artery air embolism during commercial air travel|
The neurologist 16 (2), 136-137, 2010
|Novel SPG3A and SPG4 mutations in two patients with Silver syndrome|
JS Salameh, AM Shenoy, WS David
Journal of clinical neuromuscular disease 11 (1), 57-59, 2009