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Proposal of a new diagnostic algorithm for adult-onset Still's disease.
Daghor-Abbaci K, Ait Hamadouche N, Makhloufi CD, Mechid F, Otmani F, Makrelouf M, Otmane A, Smail N, Boucelma M, Aissat FZ, Lefkir-Teffiani S, Bengana B, Boukheris N, Tebaibia A, Taharbouchet B, Ayoub S, Benziane B, Oumnia N, Haouichet C, Hanni F, Laraba N, Hakem D, Benfenatki N, Berrah A. Daghor-Abbaci K, et al. Among authors: makrelouf m. Clin Rheumatol. 2023 Apr;42(4):1125-1135. doi: 10.1007/s10067-023-06509-8. Epub 2023 Jan 25. Clin Rheumatol. 2023. PMID: 36694091
Validation of the neutrophil-to-lymphocyte ratio as a new simple biomarker of adult onset Still's disease: A STROBE-Compliant prospective observational study.
Daghor Abbaci K, Ait Hamadouche N, Otmani F, Dahou Makhloufi C, Mechid F, Makrelouf M, Otmane A, Smail N, Boucelma M, Aissat FZ, Lefkir-Teffiani S, Bengana B, Boukheris N, Tebaibia A, Taharbouchet B, Ayoub S, Benziane B, Oumnia N, Haouichet C, Hanni F, Laraba N, Hakem D, Benfenatki N, Berrah A. Daghor Abbaci K, et al. Among authors: makrelouf m. Medicine (Baltimore). 2022 Aug 12;101(32):e29970. doi: 10.1097/MD.0000000000029970. Medicine (Baltimore). 2022. PMID: 35960098 Free PMC article.
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome.
Abdi S, Bahloul A, Behlouli A, Hardelin JP, Makrelouf M, Boudjelida K, Louha M, Cheknene A, Belouni R, Rous Y, Merad Z, Selmane D, Hasbelaoui M, Bonnet C, Zenati A, Petit C. Abdi S, et al. Among authors: makrelouf m. PLoS One. 2016 Sep 1;11(9):e0161893. doi: 10.1371/journal.pone.0161893. eCollection 2016. PLoS One. 2016. PMID: 27583663 Free PMC article.
IL36RN Mutations Affect Protein Expression and Function: A Basis for Genotype-Phenotype Correlation in Pustular Diseases.
Tauber M, Bal E, Pei XY, Madrange M, Khelil A, Sahel H, Zenati A, Makrelouf M, Boubridaa K, Chiali A, Smahi N, Otsmane F, Bouajar B, Marrakchi S, Turki H, Bourrat E, Viguier M, Hamel Y, Bachelez H, Smahi A. Tauber M, et al. Among authors: makrelouf m. J Invest Dermatol. 2016 Sep;136(9):1811-1819. doi: 10.1016/j.jid.2016.04.038. Epub 2016 May 21. J Invest Dermatol. 2016. PMID: 27220475 Free article. Review.
IFN-γ and TNF-α are involved during Alzheimer disease progression and correlate with nitric oxide production: a study in Algerian patients.
Belkhelfa M, Rafa H, Medjeber O, Arroul-Lammali A, Behairi N, Abada-Bendib M, Makrelouf M, Belarbi S, Masmoudi AN, Tazir M, Touil-Boukoffa C. Belkhelfa M, et al. Among authors: makrelouf m. J Interferon Cytokine Res. 2014 Nov;34(11):839-47. doi: 10.1089/jir.2013.0085. Epub 2014 May 15. J Interferon Cytokine Res. 2014. PMID: 24831467
EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.
Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C. Behlouli A, et al. Among authors: makrelouf m. Orphanet J Rare Dis. 2014 Apr 17;9:55. doi: 10.1186/1750-1172-9-55. Orphanet J Rare Dis. 2014. PMID: 24741995 Free PMC article.
16 results