Reda Ouazzani
Overview
Explore the profile of Reda Ouazzani including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
387
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0
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Recent Articles
1.
Souirti Z, Hmidani M, Lamkadddem A, Khabbach K, Belakhdar S, Charkani D, et al.
Epilepsia Open
. 2023 Oct;
8(4):1340-1349.
PMID: 37805672
Objective: In Morocco, there was a lack of data related to the epidemiology of epilepsy. This data serves as a useful basis for the development of any national intervention or...
2.
Beddaa H, Kably B, Mouhi I, Marzouk B, Marfak A, Nafai S, et al.
Pan Afr Med J
. 2022 Aug;
42:61.
PMID: 35949472
Introduction: the validity of the upper limb neurodynamic tests and especially the upper limb neurodynamic test 1 for diagnosing carpal tunnel syndrome has been the subject of several previous studies....
3.
Kissani N, Rhazouani O, Souirti Z, Khramaz M, Meryem C, Mebrouk Y, et al.
Epilepsia Open
. 2021 Mar;
6(1):13-21.
PMID: 33681643
The World Health Organization (WHO) estimates that about 50 million people of all ages have epilepsy and nearly 85% of whom live in low- and middle-income (LMICs) countries. In Morocco,...
4.
Idrissi A, Lamkaddem A, Benouajjit A, Ben El Bouaazzaoui M, El Houari F, Alami M, et al.
Sleep Med
. 2020 Aug;
74:248-253.
PMID: 32862008
Background: The lockdown of COVID-19 (Coronavirus Disease 2019) is associated with several stressful factors that can negatively affect peoples' sleep quality and mental health. Objectives: We conducted this study to...
5.
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...
6.
Khetarpal S, Schjoldager K, Christoffersen C, Raghavan A, Edmondson A, Reutter H, et al.
Cell Metab
. 2016 Aug;
24(2):234-45.
PMID: 27508872
Human genetics studies have implicated GALNT2, encoding GalNAc-T2, as a regulator of high-density lipoprotein cholesterol (HDL-C) metabolism, but the mechanisms relating GALNT2 to HDL-C remain unclear. We investigated the impact...
7.
Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers D, Veriepe J, et al.
Am J Hum Genet
. 2016 Jun;
98(6):1271.
PMID: 27259058
No abstract available.
8.
Gan-Or Z, Bouslam N, Birouk N, Lissouba A, Chambers D, Veriepe J, et al.
Am J Hum Genet
. 2016 May;
98(5):1038-1046.
PMID: 27153400
Hereditary spastic paraplegia (HSP) is a genetically and clinically heterogeneous disease characterized by spasticity and weakness of the lower limbs with or without additional neurological symptoms. Although more than 70...
9.
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,...
10.
Gauthier J, Bencheikh B, Hamdan F, Harrison S, Baker L, Couture F, et al.
Eur J Hum Genet
. 2014 Nov;
23(9):1266-8.
PMID: 25407000
Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is characterized by marked dilatation of the bladder and microcolon and decreased intestinal peristalsis. Recent studies indicate that heterozygous variants in ACTG2, which codes for a...