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
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Reticulon 2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity.
Brain. 2024 Mar 25:awae091. doi: 10.1093/brain/awae091. Online ahead of print.
Brain. 2024.
PMID: 38527963
MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy.
Pujol C, Lebigot E, Gaignard P, Galai S, Kraoua I, Bault JP, Dard R, Youssef-Turki IB, Omar S, Boutron A, Wai T, Slama A.
Pujol C, et al. Among authors: youssef turki ib.
Brain. 2023 Mar 1;146(3):858-864. doi: 10.1093/brain/awac444.
Brain. 2023.
PMID: 36417180
Free PMC article.
Item in Clipboard
Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.
Kraoua I, Bouyacoub Y, Drissi C, Chargui M, Rebai I, Chebil A, Klaa H, Benrhouma H, Hassen A, Gouider-Khouja N, Abdelhak S, Boespflug-Tanguy O, Youssef-Turki IB, Dorboz I.
Kraoua I, et al. Among authors: youssef turki ib.
Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30.
Neuropediatrics. 2021.
PMID: 34192786
Review.
Item in Clipboard
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology.
Lahbib S, Leblond CS, Hamza M, Regnault B, Lemée L, Mathieu A, Jaouadi H, Mkaouar R, Youssef-Turki IB, Belhadj A, Kraoua I, Bourgeron T, Abdelhak S.
Lahbib S, et al. Among authors: youssef turki ib.
J Appl Genet. 2019 Feb;60(1):49-56. doi: 10.1007/s13353-018-0472-3. Epub 2018 Oct 4.
J Appl Genet. 2019.
PMID: 30284680
Item in Clipboard
Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review.
Younes TB, Benrhouma H, Klaa H, Rouissi A, Chaabouni M, Kraoua I, Youssef-Turki IB.
Younes TB, et al. Among authors: youssef turki ib.
Neuropediatrics. 2018 Oct;49(5):339-341. doi: 10.1055/s-0038-1667024. Epub 2018 Jul 16.
Neuropediatrics. 2018.
PMID: 30011403
Review.
Item in Clipboard
A Case of Progressive Chorea Resulting From GLUT1 Deficiency.
Kraoua I, Benrhouma H, Vuillaumier-Barrot S, Klaa H, Youssef-Turki IB.
Kraoua I, et al. Among authors: youssef turki ib.
Mov Disord Clin Pract. 2015 Aug 18;2(4):424-425. doi: 10.1002/mdc3.12191. eCollection 2015 Dec.
Mov Disord Clin Pract. 2015.
PMID: 30363555
Free PMC article.
No abstract available.
Item in Clipboard
[An overview of neurometabolic diseases in Tunisia. a 3-year prospective study].
Kraoua I, Benrhouma H, Rouissi A, Youssef-Turki IB, Zouari B, Kaabachi N, Gouider-Khouja N.
Kraoua I, et al. Among authors: youssef turki ib.
Rev Neurol (Paris). 2009 Jun-Jul;165(6-7):568-74. doi: 10.1016/j.neurol.2008.10.027. Epub 2009 Jan 24.
Rev Neurol (Paris). 2009.
PMID: 19168196
French.
Item in Clipboard
Cite
Cite