Detalhe da pesquisa
1.
Trends in the consumption and cost of antiepileptics in Morocco between 2008 and 2018.
Rev Epidemiol Sante Publique
; 70(2): 75-81, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35337700
2.
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Am J Hum Genet
; 98(5): 1038-1046, 2016 May 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27153400
3.
Contribution of fibrin glue in the surgery of cyanogenic and non-cyanogenic congenital cardiopathies: retrospective cohort study.
BMC Cardiovasc Disord
; 19(1): 117, 2019 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31096916
4.
Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.
Am J Hum Genet
; 91(6): 1051-64, 2012 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23176821
5.
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction.
J Med Genet
; 51(2): 137-42, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24319291
6.
[Clinical and environmental aspects of amyotrophic lateral sclerosis in moroccan population: a study of 60 cases]. / Aspects cliniques et environnementaux de la sclérose latérale amyotrophique chez une population morocaine: etude de 60 cas.
Tunis Med
; 93(6): 365-70, 2015 Jun.
Artigo
em Francês
| MEDLINE | ID: mdl-26644099
7.
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Am J Hum Genet
; 98(6): 1271, 2016 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27259058
8.
Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome.
Genet Test Mol Biomarkers
; 28(6): 257-262, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38721948
9.
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.
J Mol Neurosci
; 73(6): 391-402, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37256495
10.
An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3.
BMC Med Genet
; 13: 18, 2012 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22436252
11.
Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.
Am J Hum Genet
; 82(4): 992-1002, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18394578
12.
Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.
J Mol Neurosci
; 71(1): 142-152, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32557143
13.
Locked in syndrome revealing an antiphospholipid syndrome.
Tunis Med
; 93(1): 47-8, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25955371
14.
[Current antiplatelet agents, new inhibitors and therapeutic targets]. / Antiplaquettaires actuels, en cours de développement et cibles thérapeutiques.
Med Sci (Paris)
; 36(4): 348-357, 2020 Apr.
Artigo
em Francês
| MEDLINE | ID: mdl-32356711
15.
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.
Neurogenetics
; 10(1): 35-42, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18758830
16.
A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis.
Pan Afr Med J
; 33: 2, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31303947
17.
Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
Brain
; 130(Pt 4): 1062-75, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17347251
18.
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.
Case Rep Genet
; 2018: 8635698, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30581635
19.
Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients.
Front Neurol
; 9: 170, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29670566
20.
Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat.
Front Neurol
; 9: 532, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30108543