Majdi Nagara
Overview
Explore the profile of Majdi Nagara including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
205
Followers
0
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Recent Articles
1.
Zawati I, Adouni O, Manai M, Nagara M, Tacam M, Reduzzi C, et al.
Hum Immunol
. 2022 Sep;
83(12):843-856.
PMID: 36068099
Classical Hodgkin lymphoma (CHL) is characterized by extensive inflammatory immune cells, which predict the disease prognosis. Therefore, this study aimed to explore the significance of different tumor-infiltrated immune cells and...
2.
Jaouadi H, Bouyacoub Y, Chabrak S, Kraoua L, Zaroui A, Elouej S, et al.
Herz
. 2020 Jan;
46(Suppl 1):94-102.
PMID: 31970460
Unexplained sudden death in the young is cardiovascular in most cases. Structural and conduction defects in cardiac-related genes can conspire to underlie sudden cardiac death. Here we report a clinical...
3.
Zaravinos A, Roufas C, Nagara M, de Lucas Moreno B, Oblovatskaya M, Efstathiades C, et al.
J Exp Clin Cancer Res
. 2019 Aug;
38(1):364.
PMID: 31429779
Background: Microsatellite unstable colorectal cancers (MSI+ CRCs) expressing PD-L1, respond to anti-PD-1 or anti-PD-L1 checkpoint blockade, whereas microsatellite-stable tumors do not respond the same. Our aim was to examine how...
4.
Hamdi Y, Ben Rekaya M, Jingxuan S, Nagara M, Messaoud O, Elgaaied A, et al.
BMC Cancer
. 2018 Dec;
18(1):1295.
PMID: 30594178
Background: Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels...
5.
Mignon-Ravix C, Milh M, Kaiser C, Daniel J, Riccardi F, Cacciagli P, et al.
Hum Mutat
. 2018 Apr;
39(7):934-938.
PMID: 29663568
Early myoclonic epilepsy (EME) or Aicardi syndrome is one of the most severe epileptic syndromes affecting neonates. We performed whole exome sequencing in a sporadic case affected by EME and...
6.
Ben Rekaya M, Naouali C, Messaoud O, Jones M, Bouyacoub Y, Nagara M, et al.
J Dermatol Sci
. 2017 Nov;
89(2):172-180.
PMID: 29169765
Background: Skin cancers (SC) are complex diseases that develop from complex combinations of genetic and environmental risk factors. One of the most severe and rare genetic diseases predisposing to SC...
7.
Nagara M, Papagregoriou G, Ben Abdallah R, Landoulsi Z, Bouyacoub Y, Elouej S, et al.
Eur J Med Genet
. 2017 Oct;
61(1):1-7.
PMID: 29024829
Aim Of The Study: Recent advances in understanding the underlying molecular mechanism for distal renal tubular acidosis (dRTA), led to an increased attention towards the primary and the familial forms...
8.
Ben Halima Y, Kefi R, Sazzini M, Giuliani C, De Fanti S, Nouali C, et al.
Genes Nutr
. 2017 Sep;
12:20.
PMID: 28855970
Background: The ability to digest lactose after weaning, namely, lactase persistence (LP), is encoded by polymorphisms in the gene and varies widely in frequency among different human populations. Although, evolution...
9.
Kefi R, Hechmi M, Dallali H, Elouej S, Jmel H, Ben Halima Y, et al.
Ann Endocrinol (Paris)
. 2017 Jun;
78(3):146-155.
PMID: 28624160
Aim Of The Study: APOA5 has been linked to metabolic syndrome (MetS) or its traits in several populations. In North Africa, only the Moroccan population was investigated. Our aim is...
10.
Elouej S, Rejeb I, Attaoua R, Nagara M, Sallem O, Kamoun I, et al.
Endocr Res
. 2016 Feb;
41(4):300-309.
PMID: 26905813
Aim Of The Study: Recent genome-wide association studies (GWASs) have identified many genetic variants associated with metabolic syndrome (MetS). However, their contribution to MetS in ethnic groups in Tunisia is...