Halima Belaidi
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Explore the profile of Halima Belaidi including associated specialties, affiliations and a list of published articles.
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5
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34
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Recent Articles
1.
Albakaye M, Belaidi H, Lahjouji F, Errguig L, Kuate C, Maiga Y, et al.
Epilepsy Behav
. 2018 Feb;
80:184-190.
PMID: 29414550
Introduction: The hemiconvulsion-hemiplegia-epilepsy (HHE) syndrome is a rare consequence of febrile seizures during childhood. It is characterized by the presence of prolonged unilateral clonic seizures occurring during febrile illness in...
2.
Ghchime R, Benjelloun H, Kiai H, Belaidi H, Lahjouji F, Ouazzani R
Epilepsy Res Treat
. 2016 Mar;
2016:7417540.
PMID: 27006827
It is well established that the temporal lobe epilepsy (TLE) is linked to the autonomic nervous system dysfunctions. Seizures alter the function of different systems such as the respiratory, cardiovascular,...
3.
Rahmani M, Belaidi H, Benabdeljlil M, Bouchhab W, El Jazouli N, El Brini A, et al.
BMC Pharmacol Toxicol
. 2013 Dec;
14:61.
PMID: 24314014
Background: Carbon monoxide (CO) intoxication is a leading cause of severe neuropsychological impairments. Peripheral nerve injury has rarely been reported. It consists usually in a demyelinating polyneuropathy or mononeuropathy affecting...
4.
Moulard B, Genton P, Grid D, Jeanpierre M, Ouazzani R, Mrabet A, et al.
Hum Genet
. 2002 Sep;
111(3):255-62.
PMID: 12215838
Unverricht-Lundborg disease (ULD) is a progressive myoclonus epilepsy common in Finland and North Africa, and less common in Western Europe. ULD is mostly caused by expansion of a dodecamer repeat...
5.
Benomar A, Yahyaoui M, Meggouh F, Bouhouche A, Boutchich M, Bouslam N, et al.
J Neurol Sci
. 2002 Jun;
198(1-2):25-9.
PMID: 12039660
Fifteen Moroccan families with a phenotype resembling Friedreich Ataxia (FA) were studied. Seven families (13 patients) had the 744 del A mutation in the alpha-tocopherol transfer protein (alpha-TTP) gene, characteristic...