Search Results - "Elwafa, Reham Abdel Haleem Abo"

Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life by Elshafey, Samar Atef, Thabet, Mohamed Alaa Eldin Hassan, Abo Elwafa, Reham Abdel Haleem, Schneider, Ronen, Shril, Shirlee, Buerger, Florian, Hildebrandt, Friedhelm, Fathy, Hanan M

“…Aim The earlier the onset of proteinuria, the higher the incidence of genetic forms. Therefore, we aimed to analyse the spectrum of monogenic proteinuria in…”
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Evaluation of Sigma metric approach for monitoring the performance of automated analyzers in hematology unit of Alexandria Main University Hospital by Ahmed El‐Neanaey, Wafaa, Mahmoud AbdEllatif, Nihal, Abdel Haleem Abo Elwafa, Reham

“…Introduction Sigma metric offers a quantitative framework for evaluating process performance in clinical laboratories. This study aimed to evaluate the…”
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Cyclin D2 gene variance and expression level in pediatric acute lymphoblastic leukemia by Elwafa, Reham Abdel Haleem Abo, Bordiny, Magdy El, Salama, Mostafa, Fawzy, Amira, Omar, Omneya Magdy

“…Abstract Background Cyclin D2 (CCND2) is a crucial player in cell cycle regulation. CCND2 polymorphisms contribute to cancer predisposition. Objectives To…”
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Manual method versus flow cytometry for diagnosing spontaneous bacterial peritonitis by Moheb, Islam, Hassouna, Ehab Moustafa, El-Gohary, Iman Ezzat, Elwafa, Reham Abdel Haleem Abo, Kamal, Ahmed

“…ABSTRACTBackground Diagnosing spontaneous bacterial peritonitis (SBP) requires a high clinical index of suspicion because the clinical presentation varies…”
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Study of the Relationship between Serum Asprosin, Endothelial Dysfunction and Insulin Resistance by Rohoma, Kamel Hemida, Abdellrahim, Aly Ahmed, Abo Elwafa, Reham Abdel Haleem, Moawad, Mohamed Galal

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A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE‐1 insertion in LDLR by Song, Yongjun, Elwafa, Reham Abdel Haleem Abo, Omar, Omneya Magdy, Seo, Go Hun, Lee, Hane

“…Background Familial hypercholesterolemia (MIM: PS143890) is a genetic disorder characterized by an increase in blood cholesterol. LDLR is one of the genes…”
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Study of the influence of heme oxygenase 1 gene single nucleotide polymorphism (rs2071746) on esophageal varices among patients with cirrhosis by Ellakany, Walid Ismail, Mahmoud MoheyEldin, Khaled, Invernizzi, Pietro, Mahmoud ElKady, Ali, Eldin Fathy Abou Elkheir, Hossam, Abdel Haleem Abo Elwafa, Reham, Ellakany, Ahmed

“…INTRODUCTIONCirrhosis as a pathological term has some criteria known to be common in all cases of liver cirrhosis. Esophageal varices are portosystemic…”
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PIK3CA Polymorphism (rs17849079 C/T) and Expression in Breast cancer Patients by Hanafy, Shaden Muawia, Abo Elwafa, Reham Abdel Haleem, Abdelkader, Ahmed Abdellatif, Alowiri, Nabil Hadi

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BONE MINERAL DENSITY AND VITAMIN D RECEPTOR GENETIC VARIANTS IN EGYPTIAN CHILDREN WITH BETA THALASSEMIA ON VITAMIN D SUPPLEMENTATION by Abbassy, Hadeer A, Abo Elwafa, Reham Abdel Haleem, Omar, Omneya Magdy

“…Background: Low bone mineral density (BMD) is a characteristic feature of Beta thalassemia major (βTM) patients. Vitamin D is important for bone…”
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Plasma soluble CD 163 level as a marker of oesophageal varices in cirrhotic patients by El Din Mohamed Abdo, Alaa, Mahmoud Mohy El Din, Khaled, El Din Saeed Bedewy, Essam, Abdel Haleem Abo Elwafa, Reham, Adel Abdel Aziz, Mohamed

“…Variceal bleeding (VB), the most common lethal complication of cirrhosis, associated with high mortality. Timely prediction of esophageal varices (EV)…”
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Evaluation of non-thyroidal illness syndrome in shock patients admitted to pediatric intensive care unit in a developing country by El-Nawawy, Ahmed, Elwafa, Reham Abdel Haleem Abo, Khalil Abouahmed, Ahmed, Rasheed, Rehab Atef, Omar, Omneya Magdy

“…During critical illness, children my experience various changes in their thyroid hormone levels. Such changes are termed non-thyroidal illness syndrome (NTI)…”
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Late Endocrine Disorders of Childhood Brain and Neck Cancer Survivors by Omar, Omneya Magdy, Aron, Dotto, Elwafa, Reham Abdel Haleem Abo, Fadel, Shady Hassan, Raafat, Shaymaa

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Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2years of life by Samar Atef Elshafey, Mohamed Alaa Eldin Hassan Thabet, Reham Abdel Haleem Abo Elwafa, Schneider, Ronen, Shril, Shirlee, Buerger, Florian, Hildebrandt, Friedhelm, Fathy, Hanan M

“…AimThe earlier the onset of proteinuria, the higher the incidence of genetic forms. Therefore, we aimed to analyse the spectrum of monogenic proteinuria in…”
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Faecal calprotectin in COVID-19 patients with intestinal symptoms by Ellakany, Walid Ismail, AbdelHady, Ahmed Mohamed, Nassar, Mohamed Wael, Elwafa, Reham Abdel Haleem Abo

“…Extra-pulmonary manifestations of the Coronavirus disease of 2019 (COVID-19) have been increasingly reported, especially gastrointestinal and hepatic system…”
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KRAS mutations in patients with AML: clinical characteristics and not reported mutations using NGS by Ibrahim Elsayed, Salma Said, Deghady, Akram Abdel-Moneim, Elneily, Dalia AbdElmoat, AboElwafa, Reham Abdel Haleem

“…Background AML is a complex and heterogeneous disease. The KRAS gene is one of the important genes in the pathogenesis of acute myeloid leukemia (AML). Mutant…”
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