Detalhe da pesquisa
1.
Neuronal ceroïd-lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series.
Clin Genet
; 102(2): 157-160, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35796208
2.
Acute Movement Disorders in Childhood: A Cohort Study and Review of the Literature.
Pediatr Emerg Care
; 37(11): e719-e725, 2021 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34469400
3.
Muscle-Specific Kinase Autoimmune Myasthenia Gravis: Report of a Pediatric Case and Literature Review.
Neuropediatrics
; 50(2): 116-121, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30577044
4.
First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation.
Biochem Biophys Res Commun
; 497(1): 93-101, 2018 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29421650
5.
Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review.
Neuropediatrics
; 49(5): 339-341, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30011403
6.
Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome.
World J Clin Cases
; 12(3): 503-516, 2024 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38322471
7.
3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature.
Neuropediatrics
; 44(5): 281-5, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23564319
8.
Pediatric Neurotuberculosis: A cases series and review of the literature.
Eur J Paediatr Neurol
; 43: 6-11, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36739787
9.
Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort.
J Immunol Res
; 2021: 6666117, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34056010
10.
Rasmussen's Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review.
Case Rep Neurol Med
; 2020: 6810237, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32670646
11.
Childhood opsoclonus-myoclonus syndrome: A case series from Tunisia.
Brain Dev
; 39(9): 751-755, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28549713
12.
Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years.
Biomed Res Int
; 2017: 4354826, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29238716
13.
Anti-Ma2-encephalitis in a 2 year-old child: A newly diagnosed case and literature review.
Eur J Paediatr Neurol
; 19(6): 737-42, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26190012
14.
Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood.
Brain Dev
; 37(1): 153-7, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24745788
15.
Lesch Nyhan syndrome: a novel complex mutation in a Tunisian child.
Brain Dev
; 36(10): 921-3, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24503445
16.
Novel double deletions in the MECP2 gene in Tunisian Rett patient.
Gene
; 502(2): 163-7, 2012 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22561697
17.
Novel mutations in the C-terminal region of the MECP2 gene in Tunisian Rett syndrome patients.
J Child Neurol
; 27(5): 564-8, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21940684
18.
Movement disorders in neuro-metabolic diseases.
Eur J Paediatr Neurol
; 14(4): 304-7, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20015670
19.
Anti-NMDA receptor encephalitis mimicking a primary psychiatric disorder in a 13-year-old girl.
Turk Psikiyatri Derg
; 24(2): 145-7, 2013.
Artigo
em Inglês, Turco
| MEDLINE | ID: mdl-23905172