Nabila Attal
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Explore the profile of Nabila Attal including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
57
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0
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Recent Articles
1.
Benazzouz S, Benlouahmia N, Bouhadida K, Benlamara M, Arezki N, Sadeddine O, et al.
Vaccine X
. 2024 Jun;
19:100503.
PMID: 38868522
Scorpion envenoming (SE) is a public health problem in developing countries. In Algeria, the population exposed to the risk of SE was estimated at 86.45% in 2019. Thus, the development...
2.
Belkhelfa M, Bekrar S, Rezaig L, Beder N, Touri F, Yousfi Y, et al.
J Alzheimers Dis
. 2024 Jan;
97(3):1323-1339.
PMID: 38277295
Background: Alzheimer's disease (AD) is a progressive and irreversible neurodegenerative disorder. It is characterized by a gradual decrease in cognitive function and is considered a disorder in which the intensifying...
3.
Bouchtout M, Mecabih F, Boukadir C, Attal E, Daoudi S, Benkortbi H, et al.
J Clin Neuromuscul Dis
. 2023 Aug;
25(1):18-26.
PMID: 37611266
Abstract: Myasthenia gravis (MG) is an autoimmune disease of multifactorial etiology in which genetic factors and cytokines seem to play an important role. The aim of this study was to...
4.
Yagoubi A, Tahiat A, Touri N, Ladj M, Drali O, Belaid B, et al.
J Clin Immunol
. 2022 Jul;
42(8):1660-1671.
PMID: 35838820
Introduction: Inborn errors of immunity (IEI) represent a heterogeneous large group of genetic disorders characterized by susceptibility of affected individuals to recurrent infections, autoimmune/inflammatory diseases, allergy, and malignancy. We aimed...
5.
Aghamohammadi A, Rezaei N, Yazdani R, Delavari S, Kutukculer N, Topyildiz E, et al.
J Clin Immunol
. 2021 May;
41(6):1339-1351.
PMID: 34052995
Background: Inborn errors of immunity (IEIs) are a heterogeneous group of genetic defects of immunity, which cause high rates of morbidity and mortality mainly among children due to infectious and...
6.
Hamza L, Gaitch N, Sallem A, Boucekkine N, Girodon E, Oumeziane A, et al.
Andrologia
. 2020 Oct;
52(11):e13868.
PMID: 33118205
Macrozoospermia is associated with severe male infertility. To date, the only gene implicated in this phenotype is the Aurora Kinase C gene. We report in this work the genetic screening...
7.
Galleze A, Kocyigit A, Cherif N, Attal N, Touil-Boukoffa C, Raache R
Drug Chem Toxicol
. 2019 Aug;
43(2):169-173.
PMID: 31464142
The aim of this study was to assess the oxidative stress and the genotoxicity induced by chemotherapy by the determination of plasma malondialdehyde (MDA) level, protein carbonyl (PC) content, superoxide...
8.
Mihoubi E, Raache R, Amroun H, Azzouz M, Galleze A, Zaabat N, et al.
Endocr Metab Immune Disord Drug Targets
. 2019 May;
19(8):1172-1176.
PMID: 31142252
Background: We aimed to assess Vitamin D levels in patients with Type 1 Diabetes (T1D) and to investigate the correlation between vitamin D and metabolic imbalance. Material And Methods: For...
9.
Mihoubi E, Amroun H, Raache R, Bouldjennet F, Mecabih F, Azzouz M, et al.
Endocr Metab Immune Disord Drug Targets
. 2019 Feb;
19(8):1157-1164.
PMID: 30806329
Background: Diabetic nephropathy is a common worldwide multifactorial disease where involvement of genetic factors is well etablished. The aim of this study was to investigate the HLA genes implication in...
10.
Fodil D, Meyer A, Salah S, Sibilia J, Attal N, Tafiani-Lefkir S
J Clin Rheumatol
. 2016 Sep;
22(7):387-9.
PMID: 27660942
No abstract available.