Mohamed Makrelouf
Overview
Explore the profile of Mohamed Makrelouf including associated specialties, affiliations and a list of published articles.
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17
Citations
328
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Recent Articles
1.
Izemrane D, Benziane A, Makrelouf M, Hamdis N, Rabia S, Boudjellaba S, et al.
PLoS One
. 2024 Sep;
19(9):e0307824.
PMID: 39312562
Background: Glomerular filtration rate is the best indicator of renal function and a predictor of graft and patient survival after kidney transplantation. Methods: In a single-centre prospective analysis, we assessed...
2.
Daghor-Abbaci K, Laraba N, Dahou-Makhloufi C, Mechid F, Ait-Hamadouche N, Makrelouf M, et al.
Clin Rheumatol
. 2024 Sep;
43(11):3273-3283.
PMID: 39283549
Objective: To develop the Still's Disease Activity Score (SDAS). Methods: We used data from the prospective adult-onset Still's disease cohort study and evaluated the disease activity. An expert group selected...
3.
Gouaref I, Otmane A, Makrelouf M, Abderrhmane S, Haddam A, Koceir E
Int J Mol Sci
. 2024 Sep;
25(17).
PMID: 39273236
The coexistence of SAH with T2DM is a common comorbidity. In this study, we investigated the link between altered plasma antioxidant trace elements (ATE: manganese, selenium, zinc, and copper) and...
4.
Daghor-Abbaci K, Hamadouche N, Makhloufi C, Mechid F, Otmani F, Makrelouf M, et al.
Clin Rheumatol
. 2023 Jan;
42(4):1125-1135.
PMID: 36694091
Objective: This study was performed to develop a new diagnostic algorithm for adult-onset Still's disease (AOSD). Methods: We conducted a multicenter prospective nationwide case-control study in tertiary Internal Medicine, Rheumatology,...
5.
Daghor Abbaci K, Hamadouche N, Otmani F, Makhloufi C, Mechid F, Makrelouf M, et al.
Medicine (Baltimore)
. 2022 Aug;
101(32):e29970.
PMID: 35960098
This study was performed to investigate the role of neutrophil-to-lymphocyte ratio (NLR) in the diagnosis of adult onset Still disease (AOSD) and its performance to improve the sensitivity of the...
6.
Bennouar S, Bachir Cherif A, Makrelouf M, Ait Abdelkader B, Taleb A, Abdi S
Arch Osteoporos
. 2022 Jul;
17(1):100.
PMID: 35895238
Purpose/introduction: There is no consensus defining the vitamin D optimal values. The aim of this study is to establish vitamin D optimal values in the Northern Algerian population, based on...
7.
Abdi S, Bahloul A, Behlouli A, Hardelin J, Makrelouf M, Boudjelida K, et al.
PLoS One
. 2016 Sep;
11(9):e0161893.
PMID: 27583663
Usher syndrome (USH) is an autosomal recessive disorder characterized by a dual sensory impairment affecting hearing and vision. USH is clinically and genetically heterogeneous. Ten different causal genes have been...
8.
Behlouli A, Bonnet C, Abdi S, Hasbellaoui M, Boudjenah F, Hardelin J, et al.
Int J Pediatr Otorhinolaryngol
. 2016 Jul;
87:28-33.
PMID: 27368438
Congenital deafness is certainly one of the most common monogenic diseases in humans, but it is also one of the most genetically heterogeneous, which makes molecular diagnosis challenging in most...
9.
Tauber M, Bal E, Pei X, Madrange M, Khelil A, Sahel H, et al.
J Invest Dermatol
. 2016 May;
136(9):1811-1819.
PMID: 27220475
Homozygous or compound heterozygous IL36RN gene mutations underlie the pathogenesis of psoriasis-related pustular eruptions including generalized pustular psoriasis, palmoplantar pustular psoriasis, acrodermatitis continua of Hallopeau, and acute generalized exanthematous pustular...
10.
Pepermans E, Michel V, Goodyear R, Bonnet C, Abdi S, Dupont T, et al.
EMBO Mol Med
. 2014 Jun;
6(7):984-92.
PMID: 24940003
Protocadherin-15 (Pcdh15) is a component of the tip-links, the extracellular filaments that gate hair cell mechano-electrical transduction channels in the inner ear. There are three Pcdh15 splice isoforms (CD1, CD2...