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Spontaneous Viral Load Decline and Subsequent Clearance of Chronic Hepatitis C Virus in Postpartum Women Correlates With Favorable Interleukin-28B Gene Allele

Clinical infectious diseases, 2017-09, Vol.65 (6), p.999-1005

2017

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Investigating the role of VDR gene variants in multiple sclerosis susceptibility: a case–control study in Egypt

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2024-04, Vol.60 (1), p.51, Article 51

2024

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Relation of serum levels of homocysteine, vitamin B12 and folate to cognitive functions in multiple sclerosis patients

International journal of neuroscience, 2018-09, Vol.128 (9), p.835-841

2018

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Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study

Journal of medical screening, 2016-09, Vol.23 (3), p.124-129

2016

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Vitamin D receptor gene polymorphisms and idiopathic Parkinson disease: an Egyptian study

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2021-07, Vol.57 (1), Article 102

2021

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Association of CARD10 rs6000782 and TNF rs1799724 variants with paediatric-onset autoimmune hepatitis

Journal of advanced research, 2019-01, Vol.15, p.103-110

2019

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Altered expression of WFS1 and NOTCH2 genes associated with diabetic nephropathy in T2DM patients

Diabetes research and clinical practice, 2018-06, Vol.140, p.304-313

2018

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Vitamin D status in idiopathic Parkinson’s disease: an Egyptian study

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2020-05, Vol.56 (1), Article 45

2020

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Reliability of risk-based screening for hepatitis C virus infection among pregnant women in Egypt

The Journal of infection, 2015-05, Vol.70 (5), p.512-519

2015

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Serum level of cytokeratin 19 as a diagnostic and prognostic marker in patients with HCV-related hepatocellular carcinoma

Egyptian Liver Journal, 2021-06, Vol.11 (1), p.57, Article 57

2021

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Novel biomarkers for subtle myocardial involvement in type I diabetes mellitus

Cardiovascular endocrinology & metabolism, 2021-09, Vol.10 (3), p.175-181

2021

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Apolipoproteins A1 and B and their ratio in acute ischemic stroke patients with intracranial and extracranial arterial stenosis: an Egyptian study

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2020-12, Vol.56 (1), Article 115

2020

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Left ventricular diastolic dysfunction without left ventricular hypertrophy in obese children and adolescents: a Tissue Doppler Imaging and Cardiac Troponin I Study

Cardiology in the young, 2018-01, Vol.28 (1), p.76-84

2018

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Brain-derived neurotrophic factor (BDNF) gene polymorphism in a cohort of Egyptian primary open-angle glaucoma (POAG) patients

Bulletin of the National Research Centre, 2020-04, Vol.44 (1), p.1-7, Article 45

2020

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Lysosomal Storage Disorders in Egyptian Children

Indian journal of pediatrics, 2016-08, Vol.83 (8), p.805-813

2016

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Association between laboratory markers, clinical and radiological findings in patients with idiopathic intracranial hypertension: case–control study

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2024-09, Vol.60 (1), p.115, Article 115

2024

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Identification of insulin gene variants in neonatal diabetes

The journal of maternal-fetal & neonatal medicine, 2017-05, Vol.30 (9), p.1035-1040

2017

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Urinary interleukin-6 and tumour necrosis factor-alpha as early markers for diabetic nephropathy in children and adolescents with type 1 diabetes

Sri Lanka journal of child health, 2020-09, Vol.49 (3), p.269

2020

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Effect of interleukin-10 gene promoter polymorphisms -1082 G/A and -592 C/A on response to therapy in children and adolescents with chronic hepatitis C virus infection

Human immunology, 2016-12, Vol.77 (12), p.1248-1253

2016

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Hepatitis C Virus (HCV) Vertical Transmission in 12-Month-Old Infants Born to HCV-Infected Women and Assessment of Maternal Risk Factors

Open forum infectious diseases, 2015-04, Vol.2 (2), p.ofv089-ofv089

2015

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Validation of a Proposed Warfarin Dosing Algorithm Based on the Genetic Make-Up of Egyptian Patients

Molecular diagnosis & therapy, 2013-12, Vol.17 (6), p.381-390

2013

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Sorption behavior of Co-radionuclides from radioactive waste solution on graphene enhanced by immobilized sugarcane and carboxy methyl cellulose

Radiochimica acta, 2019-05, Vol.107 (5), p.397-413

2019

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Multiple sclerosis and fecundity: a study of anti-mullerian hormone level in Egyptian patients

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2023-10, Vol.59 (1), p.141, Article 141

2023

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Vitamin D and its binding protein in children with cystic fibrosis: A single center study

The Gazette of the Egyptian Paediatric Association, 2016-09, Vol.64 (3), p.131-135

2016

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Gene mutations in Wilson disease in Egyptian children: Report on two novel mutations

Arab journal of gastroenterology, 2014-09, Vol.15 (3-4), p.114-118

2014

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Spontaneous Viral Load Decline and Subsequent Clearance of Chronic Hepatitis C Virus in Postpartum Women Correlates With Favorable Interleukin-28B Gene Allele

Investigating the role of VDR gene variants in multiple sclerosis susceptibility: a case–control study in Egypt

Relation of serum levels of homocysteine, vitamin B12 and folate to cognitive functions in multiple sclerosis patients

Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study

Vitamin D receptor gene polymorphisms and idiopathic Parkinson disease: an Egyptian study

Association of CARD10 rs6000782 and TNF rs1799724 variants with paediatric-onset autoimmune hepatitis

Altered expression of WFS1 and NOTCH2 genes associated with diabetic nephropathy in T2DM patients

Vitamin D status in idiopathic Parkinson’s disease: an Egyptian study

Reliability of risk-based screening for hepatitis C virus infection among pregnant women in Egypt

Serum level of cytokeratin 19 as a diagnostic and prognostic marker in patients with HCV-related hepatocellular carcinoma

Novel biomarkers for subtle myocardial involvement in type I diabetes mellitus

Apolipoproteins A1 and B and their ratio in acute ischemic stroke patients with intracranial and extracranial arterial stenosis: an Egyptian study

Left ventricular diastolic dysfunction without left ventricular hypertrophy in obese children and adolescents: a Tissue Doppler Imaging and Cardiac Troponin I Study

Brain-derived neurotrophic factor (BDNF) gene polymorphism in a cohort of Egyptian primary open-angle glaucoma (POAG) patients

Lysosomal Storage Disorders in Egyptian Children

Association between laboratory markers, clinical and radiological findings in patients with idiopathic intracranial hypertension: case–control study

Identification of insulin gene variants in neonatal diabetes

Urinary interleukin-6 and tumour necrosis factor-alpha as early markers for diabetic nephropathy in children and adolescents with type 1 diabetes

Effect of interleukin-10 gene promoter polymorphisms -1082 G/A and -592 C/A on response to therapy in children and adolescents with chronic hepatitis C virus infection

Hepatitis C Virus (HCV) Vertical Transmission in 12-Month-Old Infants Born to HCV-Infected Women and Assessment of Maternal Risk Factors

Validation of a Proposed Warfarin Dosing Algorithm Based on the Genetic Make-Up of Egyptian Patients

Sorption behavior of Co-radionuclides from radioactive waste solution on graphene enhanced by immobilized sugarcane and carboxy methyl cellulose

Multiple sclerosis and fecundity: a study of anti-mullerian hormone level in Egyptian patients

Vitamin D and its binding protein in children with cystic fibrosis: A single center study

Gene mutations in Wilson disease in Egyptian children: Report on two novel mutations

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