ติดตาม
Dimah Saade
Dimah Saade
ยืนยันอีเมลแล้วที่ nih.gov
ชื่อ
อ้างโดย
อ้างโดย
ปี
PIEZO2 mediates injury-induced tactile pain in mice and humans
M Szczot, J Liljencrantz, N Ghitani, A Barik, R Lam, JH Thompson, ...
Science translational medicine 10 (462), eaat9892, 2018
2642018
PIEZO2 in sensory neurons and urothelial cells coordinates urination
KL Marshall, D Saade, N Ghitani, AM Coombs, M Szczot, J Keller, T Ogata, ...
Nature 588 (7837), 290-295, 2020
1632020
An ultrafast system for signaling mechanical pain in human skin
SS Nagi, AG Marshall, A Makdani, E Jarocka, J Liljencrantz, ...
Science advances 5 (7), eaaw1297, 2019
1302019
Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis
P Mohassel, S Donkervoort, MA Lone, M Nalls, K Gable, SD Gupta, ...
Nature medicine 27 (7), 1197-1204, 2021
1282021
Pure cannabidiol in the treatment of malignant migrating partial seizures in infancy: a case report
D Saade, C Joshi
Pediatric neurology 52 (5), 544-547, 2015
662015
Expanding the comprehensive national neonatal screening programme in the United Arab Emirates from 1995 to 2011
H Al Hosani, M Salah, HM Osman, HM Farag, L El-Assiouty, D Saade, ...
East Mediterr Health J 20 (1), 17-23, 2014
652014
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency
AP Rebelo, D Saade, CV Pereira, A Farooq, TC Huff, L Abreu, CT Moraes, ...
Brain 141 (3), 662-672, 2018
612018
The national congenital anomalies register in the United Arab Emirates
H Al Hosani, M Salah, H Abu-Zeid, HM Farag, D Saade
East Mediterr Health J 11 (4), 690-9, 2005
612005
Safety and efficacy of gene replacement therapy for X-linked myotubular myopathy (ASPIRO): a multinational, open-label, dose-escalation trial
PB Shieh, NL Kuntz, JJ Dowling, W Müller-Felber, CG Bönnemann, ...
The Lancet Neurology 22 (12), 1125-1139, 2023
602023
GMPPB‐Associated Dystroglycanopathy: Emerging Common Variants with Phenotype Correlation
BS Jensen, T Willer, DN Saade, MO Cox, T Mozaffar, M Scavina, ...
Human mutation 36 (12), 1159-1163, 2015
532015
PIEZO2 in somatosensory neurons controls gastrointestinal transit
MR Servin-Vences, RM Lam, A Koolen, Y Wang, DN Saade, M Loud, ...
Cell 186 (16), 3386-3399. e15, 2023
492023
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
S Donkervoort, R Sabouny, P Yun, L Gauquelin, KR Chao, Y Hu, ...
Acta neuropathologica 138, 1013-1031, 2019
392019
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
MC Estañ, E Fernández-Núñez, MS Zaki, MI Esteban, S Donkervoort, ...
Nature communications 10 (1), 797, 2019
372019
United Arab Emirates National Newborn Screening Programme: an evaluation 1998-2000.
H Al-Hosani, M Salah, D Saade, H Osman, J Al-Zahid
Eastern Mediterranean health journal= La revue de sante de la Mediterranee …, 2003
372003
Dominant collagen XII mutations cause a distal myopathy
P Mohassel, T Liewluck, Y Hu, D Ezzo, T Ogata, D Saade, S Neuhaus, ...
Annals of clinical and translational neurology 6 (10), 1980-1988, 2019
362019
Innocuous pressure sensation requires A-type afferents but not functional ΡΙΕΖΟ2 channels in humans
LK Case, J Liljencrantz, N Madian, A Necaise, J Tubbs, M McCall, ...
Nature communications 12 (1), 657, 2021
352021
Giant axonal neuropathy: cross-sectional analysis of a large natural history cohort
DX Bharucha-Goebel, G Norato, D Saade, E Paredes, V Biancavilla, ...
Brain 144 (10), 3239-3250, 2021
252021
Prevalence of iodine deficiency disorders in the United Arab Emirates measured by raised TSH levels.
H Al-Hosani, H Osman, A Wareth, D Saade, M Salah
Eastern Mediterranean Health Journal= La Revue de Sante de la Mediterranee …, 2003
242003
PIEZO2 and perineal mechanosensation are essential for sexual function
RM Lam, LJ von Buchholtz, M Falgairolle, J Osborne, E Frangos, ...
Science 381 (6660), 906-910, 2023
232023
Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy
JA Morales-Rosado, TL Schwab, SK Macklin-Mantia, AR Foley, ...
The American Journal of Human Genetics 110 (6), 989-997, 2023
232023
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