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C-Reactive Protein gene polymorphism 1468G>A (rs 1205) and the risk of Systemic Lupus Erythematosus and Lupus Nephritis

Research Abstract
NULL
Research Authors
Dalia A. Nigm, Azza A. Abo Elfadle, Marwa A.A. Galal, Khalid A. Nasif, Mohamed Z. Abd Elrahman.
Research Journal
International Journal Of Current Research
Research Pages
67807-67812
Research Publisher
NULL
Research Rank
1
Research Vol
vol 10, issue04
Research Website
NULL
Research Year
2018

C-Reactive Protein gene polymorphism 1468G>A (rs 1205) and the risk of Systemic Lupus Erythematosus and Lupus Nephritis

Research Abstract
NULL
Research Authors
Dalia A. Nigm, Azza A. Abo Elfadle, Marwa A.A. Galal, Khalid A. Nasif, Mohamed Z. Abd Elrahman.
Research Journal
International Journal Of Current Research
Research Pages
67807-67812
Research Publisher
NULL
Research Rank
1
Research Vol
vol 10, issue04
Research Website
NULL
Research Year
2018

C-Reactive Protein gene polymorphism 1468G>A (rs 1205) and the risk of Systemic Lupus Erythematosus and Lupus Nephritis

Research Abstract
NULL
Research Authors
Dalia A. Nigm, Azza A. Abo Elfadle, Marwa A.A. Galal, Khalid A. Nasif, Mohamed Z. Abd Elrahman.
Research Journal
International Journal Of Current Research
Research Pages
67807-67812
Research Publisher
NULL
Research Rank
1
Research Vol
vol 10, issue04
Research Website
NULL
Research Year
2018

Interleukin 25 and Systemic lupus erythematosus

Research Abstract
We identified that type 2 immunity stimulation has been associated with the pathogenesis of Systemic lupus Erythematous (SLE), so we studied serum level of IL 25 and its relation to SLE activity, clinical and laboratory characteristics. Methods: Serum from 90 patients who met the American College of Rheumatology (ACR) criteria for SLE and 40 healthy controls was tested for IL 25 level by Enzyme Linked Immunosorbent Assay (ELSIA). Clinical and laboratory characteristics and disease activity using SLE Disease Activity Index (SLEDAI) were also assessed. Results: IL 25 serum level was signi?cantly higher among SLE patients than healthy controls. It has statistically signi?cant correlation with disease activity. Conclusion: Our data indicates that IL 25 level is elevated in SLE patients in comparison to healthy controls and is correlated to high disease activity, potentially being a biomarker predictive for disease activity in SLE.
Research Authors
Dalia A. Nigm, Marwa A.A. Galal.
Research Journal
Journal of Clinical Immunology and Research
Research Pages
NULL
Research Publisher
SciTechnol
Research Rank
1
Research Vol
NULL
Research Website
https://www.scitechnol.com/peer-review/interleukin-25-and-systemic-lupus-erythematosus-7mqU.php?article_id=7467
Research Year
2018

Interleukin 25 and Systemic lupus erythematosus

Research Abstract
We identified that type 2 immunity stimulation has been associated with the pathogenesis of Systemic lupus Erythematous (SLE), so we studied serum level of IL 25 and its relation to SLE activity, clinical and laboratory characteristics. Methods: Serum from 90 patients who met the American College of Rheumatology (ACR) criteria for SLE and 40 healthy controls was tested for IL 25 level by Enzyme Linked Immunosorbent Assay (ELSIA). Clinical and laboratory characteristics and disease activity using SLE Disease Activity Index (SLEDAI) were also assessed. Results: IL 25 serum level was signi?cantly higher among SLE patients than healthy controls. It has statistically signi?cant correlation with disease activity. Conclusion: Our data indicates that IL 25 level is elevated in SLE patients in comparison to healthy controls and is correlated to high disease activity, potentially being a biomarker predictive for disease activity in SLE.
Research Authors
Dalia A. Nigm, Marwa A.A. Galal.
Research Journal
Journal of Clinical Immunology and Research
Research Pages
NULL
Research Publisher
SciTechnol
Research Rank
1
Research Vol
NULL
Research Website
https://www.scitechnol.com/peer-review/interleukin-25-and-systemic-lupus-erythematosus-7mqU.php?article_id=7467
Research Year
2018

B-Cell-attracting Chemokine CXCL13 as a marker of disease activity in systemic lupus erythematosus(SLE)

Research Abstract
A correlation was detected between the chemokine CXC ligand 13(CXCL13) and lupus nephritis, but there is no data recorded in literature about a relationship with other disease manifestations in systemic lupus erythematosus (SLE). Therefore, we sought to investigate the relationship between CXCL13 and overall disease activity and other disease manifestations in SLE.
Research Authors
Eman Ahmed Hamed , Eman H El-Hakeim , Marwa A A Galal ,Eman mosad , Nada Mahmoud Mostfa Nasr
Research Journal
Aktuelle Rheumatologie
Research Pages
1-6
Research Publisher
Thieme
Research Rank
1
Research Vol
42
Research Website
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0043-121875
Research Year
2017

B-Cell-attracting Chemokine CXCL13 as a marker of disease activity in systemic lupus erythematosus(SLE)

Research Abstract
A correlation was detected between the chemokine CXC ligand 13(CXCL13) and lupus nephritis, but there is no data recorded in literature about a relationship with other disease manifestations in systemic lupus erythematosus (SLE). Therefore, we sought to investigate the relationship between CXCL13 and overall disease activity and other disease manifestations in SLE.
Research Authors
Eman Ahmed Hamed , Eman H El-Hakeim , Marwa A A Galal ,Eman mosad , Nada Mahmoud Mostfa Nasr
Research Journal
Aktuelle Rheumatologie
Research Pages
1-6
Research Publisher
Thieme
Research Rank
1
Research Vol
42
Research Website
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0043-121875
Research Year
2017

B-Cell-attracting Chemokine CXCL13 as a marker of disease activity in systemic lupus erythematosus(SLE)

Research Abstract
A correlation was detected between the chemokine CXC ligand 13(CXCL13) and lupus nephritis, but there is no data recorded in literature about a relationship with other disease manifestations in systemic lupus erythematosus (SLE). Therefore, we sought to investigate the relationship between CXCL13 and overall disease activity and other disease manifestations in SLE.
Research Authors
Eman Ahmed Hamed , Eman H El-Hakeim , Marwa A A Galal ,Eman mosad , Nada Mahmoud Mostfa Nasr
Research Journal
Aktuelle Rheumatologie
Research Pages
1-6
Research Publisher
Thieme
Research Rank
1
Research Vol
42
Research Website
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0043-121875
Research Year
2017

B-Cell-attracting Chemokine CXCL13 as a marker of disease activity in systemic lupus erythematosus(SLE)

Research Abstract
A correlation was detected between the chemokine CXC ligand 13(CXCL13) and lupus nephritis, but there is no data recorded in literature about a relationship with other disease manifestations in systemic lupus erythematosus (SLE). Therefore, we sought to investigate the relationship between CXCL13 and overall disease activity and other disease manifestations in SLE.
Research Authors
Eman Ahmed Hamed , Eman H El-Hakeim , Marwa A A Galal ,Eman mosad , Nada Mahmoud Mostfa Nasr
Research Journal
Aktuelle Rheumatologie
Research Member
Research Pages
1-6
Research Publisher
Thieme
Research Rank
1
Research Vol
42
Research Website
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0043-121875
Research Year
2017

MDCT Staging of Disease Extent in Patients with Systemic Sclerosis: A Pilot Study

Research Abstract
Interstitial lung disease (ILD) is the leading cause of systemic sclerosis (SSc) related morbidity and mortality,surpassing scleroderma renal crisis, which has become a rarity following the advent of angiotensin-converting-enzyme (ACE) inhibitors.High resolution computed tomography (HRCT) is the gold standard for diagnosis of in systemic sclerosis (SSc) related interstitial lung disease (SSc-ILD).
Research Authors
A.M. Ghandour, R. M Gamal, G.S. Seifeldein, M. M M Galal, E.M. El-Hakeim
Research Journal
Annals of the Rheumatic Diseases
Research Pages
601
Research Publisher
BMJ
Research Rank
3
Research Vol
74 (suppl. 2)
Research Website
https://ard.bmj.com/content/74/Suppl_2/601.3
Research Year
2015
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