Olfa Messaoud
Overview
Explore the profile of Olfa Messaoud including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
40
Citations
240
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Mkaouar R, Riahi Z, Marrakchi J, Mezzi N, Romdhane L, Boujemaa M, et al.
Front Genet
. 2024 Jul;
15:1437233.
PMID: 38983270
[This corrects the article DOI: 10.3389/fgene.2024.1384094.].
2.
Hammami A, Bardaoui A, Eissa S, Elgaher W, Chtourou R, Messaoud O
Molecules
. 2024 Jun;
29(12).
PMID: 38930902
The current study focused on the design of an extremely sensitive electrochemical sensor of ascorbic acid based on a mixture of NiAlO-NiO nanoparticles that, produced in a single step using...
3.
Mkaouar R, Riahi Z, Marrakchi J, Mezzi N, Romdhane L, Boujemaa M, et al.
Front Genet
. 2024 May;
15:1384094.
PMID: 38711914
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily...
4.
Dallali H, Boukhalfa W, Kheriji N, Fassatoui M, Jmel H, Hechmi M, et al.
Front Endocrinol (Lausanne)
. 2024 Jan;
14:1293124.
PMID: 38192426
Introduction: Type 2 diabetes (T2D) is a multifactorial disease involving genetic and environmental components. Several genome-wide association studies (GWAS) have been conducted to decipher potential genetic aberrations promoting the onset...
5.
Khalat N, Messaoud O, Ben Rekaya M, Chargui M, Zghal M, Zendah B, et al.
Mol Genet Genomic Med
. 2023 Feb;
11(6):e2158.
PMID: 36812379
Background: Xeroderma pigmentosum is an autosomal recessive disease characterized by a high sensitivity to UV radiations. The disease is clinically and genetically heterogeneous, thus making accurate early clinical diagnosis difficult....
6.
Zaouak A, Abdessalem G, Messaoud O, Ebdelli W, Chamli A, Abdelhak S, et al.
Skinmed
. 2022 Aug;
20(4):305-306.
PMID: 35976023
A 4-year-old boy born from a consanguineous marriage was referred to our department for congenital ichthyosis. He was a collodion baby at birth and progressively developed a generalized erythroderma with...
7.
Messaoud O, Dutta A, Cornejo-Olivas M, Bhuiyan Z
Front Genet
. 2021 Dec;
12:821591.
PMID: 34966416
No abstract available.
8.
Mezzi N, Messaoud O, Mkaouar R, Zitouna N, Romdhane S, Abdessalem G, et al.
Genes (Basel)
. 2021 Nov;
12(11).
PMID: 34828426
Genetic diseases in Tunisia are a real public health problem given their chronicity and the lack of knowledge concerning their prevalence and etiology, and the high rates of consanguinity. Hence,...
9.
Mkaouar R, Riahi Z, Charfeddine C, Chelly I, Boudabbous H, Dallali H, et al.
PLoS One
. 2021 Oct;
16(10):e0258202.
PMID: 34614013
Alpha-Mannosidosis (AM) is an ultra-rare storage disorder caused by a deficiency of lysosomal alpha-mannosidase encoded by the MAN2B1 gene. Clinical presentation of AM includes mental retardation, recurrent infections, hearing loss,...
10.
Mkaouar R, Abdallah L, Naouali C, Lahbib S, Turki Z, Elouej S, et al.
Front Genet
. 2021 Sep;
12:665174.
PMID: 34539727
The role of the prokineticin 2 pathway in human reproduction, olfactory bulb morphogenesis, and gonadotropin-releasing hormone secretion is well established. Recent studies have highlighted the implication of di/oligogenic inheritance in...