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Optimizing PI Regulators for DFIGs in Wind Energy Using Artificial Intelligence

2024 2nd International Conference on Electrical Engineering and Automatic Control (ICEEAC), 2024, p.1-6

2024

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Numerical Analysis of Stratified and Slug Flows

Mathematical problems in engineering, 2021-10, Vol.2021, p.1-9

2021

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Three-Dimensional Simulations of Offshore Oil Platform in Square and Diamond Arrangements

Advances in Mathematical Physics, 2021, Vol.2021, p.1-8

2021

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A Three-Dimensional Model of Turbulent Core Annular Flow Regime

Journal of mathematics (Hidawi), 2021, Vol.2021, p.1-8

2021

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Solitary Wave Diffraction with a Single and Two Vertical Circular Cylinders

Mathematical problems in engineering, 2021-01, Vol.2021, p.1-9

2021

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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Hematology, 2016-08, Vol.21 (7), p.425-429

2016

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Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia

Blood cells, molecules, & diseases, 2013-02, Vol.50 (2), p.110-114

2013

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Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients

Biomedical papers of the Medical Faculty of the University Palacký, Olomouc, Czechoslovakia, 2015-03, Vol.159 (1), p.145-149

2015

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Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients

Tunisie Medicale, 2015-04, Vol.93 (4), p.237-241

2015

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Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia

Polish journal of pathology, 2013, Vol.64 (2), p.84-89

2013

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Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome

Hemoglobin, 2017-03, Vol.41 (2), p.147-150

2017

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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Hematology (Luxembourg), 2016-03, p.1-5

2016

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Transfusion programmée en hématologie : résultats d’une enquête de satisfaction auprès des patients polytransfusés

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2015-09, Vol.22 (4), p.241-242

2015

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Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients

Acta haematologica polonica, 2016-10, Vol.47 (4), p.242-247

2016

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Intelligent remote control of smart home devices using physiological parameters

2015 17th International Conference on E-health Networking, Application & Services (HealthCom), 2015, p.280-285

2015

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Hb H Disease Among Tunisians: Molecular Characterization of α-Thalassemia Determinants and Hematological Findings

Hemoglobin, 2003-01, Vol.27 (1), p.57-61

2003

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Optimizing PI Regulators for DFIGs in Wind Energy Using Artificial Intelligence

Numerical Analysis of Stratified and Slug Flows

Three-Dimensional Simulations of Offshore Oil Platform in Square and Diamond Arrangements

A Three-Dimensional Model of Turbulent Core Annular Flow Regime

Solitary Wave Diffraction with a Single and Two Vertical Circular Cylinders

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia

Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients

Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients

Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia

Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Transfusion programmée en hématologie : résultats d’une enquête de satisfaction auprès des patients polytransfusés

Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients

Intelligent remote control of smart home devices using physiological parameters

Hb H Disease Among Tunisians: Molecular Characterization of α-Thalassemia Determinants and Hematological Findings

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