Nadia Mahfoudh
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Explore the profile of Nadia Mahfoudh including associated specialties, affiliations and a list of published articles.
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25
Citations
405
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Recent Articles
1.
Kamoun A, Brahim R, Charfi A, Yaich S, Masmoudi M, Hakim F, et al.
Hum Immunol
. 2025 Jan;
86(2):111230.
PMID: 39793377
Introduction: HLA matching is critical for successful kidney transplantation. This study aimed to investigate the impact of eplet mismatches and Predicted Indirectly Recognizable HLA Epitopes (PIRCHE-II) scores on the development...
2.
Maaloul M, Charfi A, Feki A, Gassara Z, Hakim F, Gaddour L, et al.
Clin Rheumatol
. 2024 Dec;
44(2):707-718.
PMID: 39715961
Introduction/objectives: Psoriatic arthritis (PsA) is a chronic inflammatory rheumatism belonging to the spondyloarthritis family. It is a multifactorial disease whose genetic determinism is still poorly understood. It is favored by...
3.
Tahri S, Elloumi N, Khabou B, Frikha R, Turki H, Mahfoudh N, et al.
Arch Dermatol Res
. 2024 Jul;
316(7):449.
PMID: 38958777
Several auto-immune diseases have been linked to vitamin D deficiency as a contributing environmental factor. Its pleiotropic effects on the immune system, especially its essential role in maintaining immune tolerance,...
4.
Abida O, Elloumi N, Bahloul E, Hachicha H, Sellami K, Fakhfakh R, et al.
Mol Genet Genomic Med
. 2022 Nov;
10(12):e2080.
PMID: 36349750
Background: Almost 5% of the world's population develops an autoimmune disease (AID), it is considered the fourth leading cause of disability for women, who represent 78% of cases. The sex...
5.
Elloumi N, Tahri S, Fakhfakh R, Abida O, Mahfoudh N, Hachicha H, et al.
Ann Hum Genet
. 2022 Feb;
86(3):137-144.
PMID: 35128637
Aim: Through their recognition of various bacterial cell wall components, TLR2 and TLR4 participate in the innate response and modulate the activation of adaptive immunity. Therefore, the genetic background of...
6.
Abida O, Bahloul E, Ben Jmaa M, Sellami K, Zouidi F, Fakhfakh R, et al.
Mol Genet Genomic Med
. 2020 Sep;
8(11):e1476.
PMID: 32875738
Background: Several studies have suggested that polymorphisms within genes encoding T-lymphocyte immune regulating molecules: CD28, CTLA-4, and ICOS, may alter the signaling process and subsequently could be involved in susceptibility...
7.
Alila-Fersi O, Aloulou H, Werteni I, Mahfoudh N, Chabchoub I, Kammoun H, et al.
J Mol Neurosci
. 2020 Mar;
70(7):1100-1109.
PMID: 32125626
Pompe disease, a rare, autosomal, recessive, inherited, lysosomal storage disorder, is caused by mutations in the acid α-glucosidase (GAA) gene leading to a deficiency of the lysosomal GAA enzyme. Some...
8.
Charfi A, Mahfoudh N, Kamoun A, Frikha F, Dammak C, Gaddour L, et al.
Med Princ Pract
. 2019 Jul;
29(1):32-38.
PMID: 31272097
Objective: In order to investigate human leukocyte antigen (HLA) genes predisposing to primary Sjögren syndrome (pSS), we conducted an association study using HLA loci (A, B, and DRB1) and 9...
9.
Horer S, Marrakchi S, Radner F, Zolles G, Heinz L, Eichmann T, et al.
J Invest Dermatol
. 2019 May;
139(10):2154-2163.e5.
PMID: 31082376
Trichilemmal cysts are common hair follicle-derived intradermal cysts. The trait shows an autosomal dominant mode of transmission with incomplete penetrance. Here, we describe the pathogenetic mechanism for the development of...
10.
Neji S, Hadrich I, Ilahi A, Trabelsi H, Chelly H, Mahfoudh N, et al.
Mycopathologia
. 2018 Jul;
183(5):765-775.
PMID: 29995224
Background: The Candida parapsilosis complex species has emerged as an important cause of human disease. The molecular identification of C. parapsilosis isolates at the species level can be helpful for...