Publications

Export 17 results:
Sort by: Author Title Type [ Year (Desc)]
2021
Mousa, S. M., M. M. Makhlouf, E. t. Mohammed, and H. M. Zawam, "The Influence of Interleukin-2 Gene Polymorphisms on the Risk and Clinical Outcome of Non-Hodgkin Lymphoma", Indian Journal of Hematology and Blood Transfusion, vol. 37, issue 4, pp. 549-554, 2021.
2017
Sadek, H., I. Youssry, N. S. Ibrahim, A. A. Abou-Elalla, G. Atef, and S. M. Mousa, "The Development of FVIII Inhibitors in Relation to IL10 Gene Polymorphism in Hemophilia A Egyptian Pediatric Patients", Fetal and Pediatric Pathology, vol. 36, issue 3, pp. 184-189, 2017.
2016
Mousa, S. M., M. K. El-Ghamrawy, H. Gouda, M. Khorshied, D. A. Ahmed, and H. F. Shiba, "Prevalence of Hepatitis C among Egyptian Children with Sickle Cell Disease and the Role of IL28b Gene Polymorphisms in Spontaneous Viral Clearance.", Mediterr J Hematol Infect Dis, vol. 8, issue 1, pp. 1-6, 2016.
2015
Mousa, S. M., "Bone marrow examination in Egyptian patients with bicytopenia/pancytopenia", Comparative Clinical Pathology, vol. 24, issue 4, pp. 915-919, 2015. final_manuscript.pdf
2014
Shiba, H. F., M. K. El-Ghamrawy, I. A. E. - M. Shaheen, R. A. E. - G. Ali, and S. M. Mousa, "Glutathione S-Transferase Gene Polymorphisms (GSTM1, GSTT1, and GSTP1) in Egyptian Pediatric Patients with Sickle Cell Disease", Pediatric and Developmental Pathology, vol. 17, issue 4: The Society for Pediatric Pathology and the Paediatric Pathology Society, pp. 265 - 270, 2014. AbstractWebsite

ABSTRACT Sickle cell disease (SCD) complications are associated with oxidative stress. Glutathione S-transferases (GSTs) are a group of enzymes that protect against oxidative stress. The aims of this study was to evaluate the prevalence of GSTM1, GSTT1, and GSTP1 gene polymorphisms among homozygous sickle cell anemia patients and to investigate the possible association between the presence of these polymorphisms and SCD severity and complications. Genotyping the polymorphisms in GSTT1 and GSTM1 genes was performed using the multiplex polymerase chain reaction (PCR) method. The GSTP1 ILe105Val polymorphism was determined using PCR?restriction fragment length polymorphism. GSTM1 null genotype was significantly associated with increased risk of severe vaso-occlusive crises (VOC) (odds ratio ?=? 1.52, 95% confidence interval ?=? 0.42?5.56, P ?=? 0.005). We found no significant association between GST genotypes and frequency of sickle cell?related pain, transfusion frequency, disease severity, or hydroxyurea treatment. GSTM1 gene polymorphism may be associated with risk of severe VOC among Egyptian SCD patients.ABSTRACT Sickle cell disease (SCD) complications are associated with oxidative stress. Glutathione S-transferases (GSTs) are a group of enzymes that protect against oxidative stress. The aims of this study was to evaluate the prevalence of GSTM1, GSTT1, and GSTP1 gene polymorphisms among homozygous sickle cell anemia patients and to investigate the possible association between the presence of these polymorphisms and SCD severity and complications. Genotyping the polymorphisms in GSTT1 and GSTM1 genes was performed using the multiplex polymerase chain reaction (PCR) method. The GSTP1 ILe105Val polymorphism was determined using PCR?restriction fragment length polymorphism. GSTM1 null genotype was significantly associated with increased risk of severe vaso-occlusive crises (VOC) (odds ratio ?=? 1.52, 95% confidence interval ?=? 0.42?5.56, P ?=? 0.005). We found no significant association between GST genotypes and frequency of sickle cell?related pain, transfusion frequency, disease severity, or hydroxyurea treatment. GSTM1 gene polymorphism may be associated with risk of severe VOC among Egyptian SCD patients.

Mousa, S., S. Mostafa, I. Shahenn, and E. Elnoshokaty, "Detection of trisomy 4 and 10 in Egyptian pediatric patients with acute lymphoblastic leukemia", Clin Lab., vol. 60, issue 4, pp. 609-14, 2014.
Mousa, S. M., "Hepatitis C among Egyptian Patients Referred for Bone Marrow Examination: Seroprevalence and Analysis of Hematological Findings", Bone Marrow Research. , vol. 2014, issue Article ID 549716, pp. 4, 2014.
El-Mahgoub, E. R., E. Ahmed, R. A. - E. A. Afifi, M. - A. Kamal, and S. M. Mousa, "Mesenchymal Stem Cells from Pediatric Patients with Aplastic Anemia: Isolation, Characterization, Adipogenic, and Osteogenic Differentiation", Fetal & Pediatric Pathology, vol. 33, no. 1, pp. 9-15, 2014. AbstractWebsite

n/a

Nasef, A., M. Ibrahim, N. Riad, and S. Mousa, "Plasma annexin A5, anti-annexin A5 antibodies and annexin A5 polymorphism in Egyptian female patients with systemic lupus erythematosus and antiphospholipid syndrome.", Clin Lab., vol. 60, issue 1, pp. 133-7, 2014.
El-Din, M. - A. K., M. S. Farhan, R. I. E. Shiha, R. M. H. El-Kaffas, and S. M. Mousa, "Frequency of CYP2C9 and VKORC1 Gene Polymorphisms and Their Influence on Warfarin Dose in Egyptian Pediatric Patients", Pediatric Drugs, vol. 16, no. 4: Springer International Publishing, pp. 337-341, 2014. AbstractWebsite
n/a
2013
ElMahgoub, E. R., A. A. El-Said, EA Afifi, M. Kamal, and S. M. Mousa, "Mesenchymal Stem Cells from Pediatric Patients with Aplastic Anemia: Isolation, Characterization, Adipogenic and Osteogenic Differentiation", 4th Annual Conference of Clinical and Chemical Pathology Department (CLINCHEM 2013), Cairo, Egypt, 28 April, 2013. Abstract

n/a

2012
Farawela, H., M. Khorshied, I. Shaheen, H. Gouda, A. Nasef, N. Abulata, H. - A. Mahmoud, H. M. Zawam, and S. M. Mousa, "The association between hepatitis C virus infection, genetic polymorphisms of oxidative stress genes and B-cell non-Hodgkin’s lymphoma risk in Egypt", Infection, Genetics and Evolution: Elsevier, 2012. AbstractWebsite

n/a

Alsirafy, S. A., S. M. Mousa, and S. M. Brown, "Palliative Care An Unexplored Aspect of Schistosomiasis Neglect?", American Journal of Hospice and Palliative Medicine, vol. 29, no. 1: SAGE Publications, pp. 7–8, 2012. Abstract
n/a
2011
Metwally, H. G., R. A. El-Fattah, D. Ahmed, M. Farhan, and S. M. Mousa, "Mesenchymal stem cells derived from bone marrow and leukapheresis show different putative subpopulations", Stem Cell Studies, vol. 1, no. 1, pp. e19, 2011. Abstract
n/a
2009
El Serougy, I. M., A. A. Shahin, D. A. Soliman, A. F. Akhnoukh, and S. M. Mousa, "Clinical significance of serum anti-annexin V antibodies in Egyptian patients with scleroderma.", The Egyptian journal of immunology, vol. 16, no. 1, pp. 1, 2009. Abstract

The pathogenesis of scleroderma encompasses vascular, immunological, and fibrotic processes, which contribute to clinical manifestations. We investigated the prevalence of anti-annexin V IgG and IgM antibodies in sera of scleroderma patients and their relation to the presence of other antibodies and development of disease morbidity. Sera of 40 scleroderma patients and 15 healthy controls were examined for IgG and IgM anti-annexin V antibodies by ELISA and anticentromere antibodies by indirect immunofluorescence. Serum level of anti-annexin V IgG antibodies in scleroderma patients was significantly higher than that of the control (P < 0.001) and correlated significantly with the presence of digital ischemia (P = 0.023) and pulmonary fibrosis (P = 0.02). IgM isotype was comparable between patients and controls (P = 0.317). Anticentromere antibodies are more prevalent in the limited cutaneous subtype (P = 0.017). In conclusion, measurement of serum anti-annexin V IgG antibodies in scleroderma patients may be important for early diagnosis of vascular and pulmonary complications.

Beshlawy, A. E., H. G. Metwally, K. A. Khalek, R. F. Hammoud, and S. M. Mousa, "The effect of freezing on the recovery and expansion of umbilical cord blood hematopoietic stem cells", Experimental and Clinical Transplantation, vol. 7, no. 1, pp. 50–55, 2009. AbstractWebsite

n/a

El-Beshlawy, A., M. E. Zaki, M. HAMDY, A. Rizk, and S. M. Mousa, "Osteoporosis in beta Thalassemia Major Patients: Role of COLIA1 Gene GT Polymorphism", The Medical Journal of Cairo University, vol. 77, issue 1, pp. 193-199, 2009. AbstractWebsite

n/a

Tourism