about
Hepatitis C Virus (HCV) Vertical Transmission in 12-Month-Old Infants Born to HCV-Infected Women and Assessment of Maternal Risk Factors.Aberrant p16INK4A methylation: Relation to viral related chronic liver disease and hepatocellular carcinoma.Reliability of risk-based screening for hepatitis C virus infection among pregnant women in Egypt.Potential genetic markers for prediction of treatment response in Egyptian children infected with HCV genotype 4.High frequency of splice site mutation in 21-hydroxylase deficiency children.Lysosomal Storage Disorders in Egyptian Children.Spontaneous Viral Load Decline and Subsequent Clearance of Chronic Hepatitis C Virus in Postpartum Women Correlates With Favorable Interleukin-28B Gene Allele.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 telomerase reverse transcriptase messenger RNA (TERT mRNA) as a tumour marker for early detection of hepatocellular carcinoma.Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.Gene mutations in Wilson disease in Egyptian children: report on two novel mutations.CYP21A2 genetic profile in 14 Egyptian children with suspected congenital adrenal hyperplasia: a diagnostic challenge.Left ventricular diastolic dysfunction without left ventricular hypertrophy in obese children and adolescents: a Tissue Doppler Imaging and Cardiac Troponin I Study.Relation of serum levels of homocysteine, vitamin B12 and folate to cognitive functions in multiple sclerosis patients.Identification of insulin gene variants in neonatal diabetes.Altered expression of WFS1 and NOTCH2 genes associated with diabetic nephropathy in T2DM patients.Interleukin-18 promoter polymorphisms and idiopathic Parkinson disease: an Egyptian studyAssociation of CARD10 rs6000782 and TNF rs1799724 variants with paediatric-onset autoimmune hepatitisAssociation between serum apolipoprotein E and cognitive functions in Egyptian patients with temporal lobe epilepsy
P50
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P50
description
researcher ORCID ID = 0000-0001-9069-9545
@en
wetenschapper
@nl
name
Sahar A Sharaf
@ast
Sahar A Sharaf
@en
Sahar A Sharaf
@nl
type
label
Sahar A Sharaf
@ast
Sahar A Sharaf
@en
Sahar A Sharaf
@nl
prefLabel
Sahar A Sharaf
@ast
Sahar A Sharaf
@en
Sahar A Sharaf
@nl
P31
P496
0000-0001-9069-9545