Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
A misleading presentation of juvenile Tay Sachs disease.
Rev Neurol (Paris). 2020 Mar;176(3):213-214. doi: 10.1016/j.neurol.2019.06.011. Epub 2019 Sep 19.
Rev Neurol (Paris). 2020.
PMID: 31543363
No abstract available.
Pathologic Confirmation of Lafora Disease.
Rhouda H, Malihy A, Zouiri G, Kriouile Y.
Rhouda H, et al. Among authors: zouiri g.
Pediatr Neurol. 2020 Jul;108:128. doi: 10.1016/j.pediatrneurol.2020.02.004. Epub 2020 Feb 28.
Pediatr Neurol. 2020.
PMID: 32279901
No abstract available.
Item in Clipboard
Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder.
Rochdi K, Cerino M, Da Silva N, Delague V, Bouzidi A, Nahili H, Zouiri G, Kriouile Y, Gorokhova S, Bartoli M, Saïle R, Barakat A, Krahn M.
Rochdi K, et al. Among authors: zouiri g.
Clin Chim Acta. 2022 Jan 1;524:51-58. doi: 10.1016/j.cca.2021.11.020. Epub 2021 Nov 28.
Clin Chim Acta. 2022.
PMID: 34852264
Item in Clipboard
[Guillain-Barré syndrome with preserved reflexes].
Zouiri G, Abilkassem R, Zerhouni A, Dini N, Agadr A.
Zouiri G, et al.
Arch Pediatr. 2016 May;23(5):501-3. doi: 10.1016/j.arcped.2016.02.019. Epub 2016 Mar 24.
Arch Pediatr. 2016.
PMID: 27021810
French.
Item in Clipboard
c.754T>A homozygous mutation described for the first time in three Moroccan patients with Gaucher disease.
Zouiri G, Rhouda H, Kriouile Y.
Zouiri G, et al.
Arch Pediatr. 2024 May;31(4):277-278. doi: 10.1016/j.arcped.2023.11.002. Epub 2024 Mar 13.
Arch Pediatr. 2024.
PMID: 38485567
Item in Clipboard
Cite
Cite