Yasmine Elshiwy
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View article: Copy Number Variations in Genetic Diagnosis of Congenital Adrenal Hyperplasia Children
Copy Number Variations in Genetic Diagnosis of Congenital Adrenal Hyperplasia Children Open
Background: Congenital adrenal hyperplasia (CAH) is a monogenic disorder caused by genetic diversity in the CYP21A2 gene, with 21-hydroxylase deficiency (21-OHD) as the most common type. Early sex assignment and early diagnosis of differen…
View article: Mass spectrometry: an essential tool to be used in discrimination between causes of congenital adrenal hyperplasia, and its benefits versus radioimmunoassay
Mass spectrometry: an essential tool to be used in discrimination between causes of congenital adrenal hyperplasia, and its benefits versus radioimmunoassay Open
Background Measurement of multiple steroids, 17 hydroxyprogesterone, 11 deoxycortisol, and 21 deoxycortisol, is required to discriminate between congenital adrenal hyperplasia due to 21 hydroxylase deficiency and that due to 11 beta hydrox…
View article: MicroRNAs and Risk Factors for Diabetic Nephropathy in Egyptian Children and Adolescents with Type 1 Diabetes
MicroRNAs and Risk Factors for Diabetic Nephropathy in Egyptian Children and Adolescents with Type 1 Diabetes Open
Shereen Abdelghaffar,1 Hassan Shora,2 Sahar Abdelatty,3 Fatma Elmougy,3 Reham El Sayed,3 Heba Abdelrahman,3 Hend Soliman,1 HebatAllah Algebaly,1 Sakinatalfouad Ahmed,1 Peter Alfy,1 Yasmine Elshiwy3 1Department of Pediatrics, Cairo Universi…
View article: <p>MicroRNAs and Risk Factors for Diabetic Nephropathy in Egyptian Children and Adolescents with Type 1 Diabetes</p>
MicroRNAs and Risk Factors for Diabetic Nephropathy in Egyptian Children and Adolescents with Type 1 Diabetes Open
miRNA-377, miRNA-93, miRNA-216a, and miRNA-21 may be implicated in the pathogenesis of DN, while miRNA-25 may have a reno-protective role. More studies are needed to document the value of these miRNAs as diagnostic biomarkers as well as th…
View article: Salivary Antisense Non-Coding RNA In the INK4 Locus & Maternal Expressed Gene 3 as early biomarkers in Detection of Malignant Transformation of Oral Lichen Planus
Salivary Antisense Non-Coding RNA In the INK4 Locus & Maternal Expressed Gene 3 as early biomarkers in Detection of Malignant Transformation of Oral Lichen Planus Open
Oral lichen planus (OLP) is a potentially malignant lesion.It is crucial to properly identify patients at risk of malignant transformation.LncRNA antisense non-coding RNA in the INK4 locus (ANRIL) has been known to advance tumor progressio…