Search Results - "Omar, Omneya Magdy"
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The malnutrition screening tool STRONGKIDS performed better than other screening tools for children hospitalised in Egypt
Published in Acta Paediatrica (01-05-2024)“…Aim To compare the accuracy of three different screening tools, namely, the Paediatric Yorkhill Malnutrition Score (PYMS), Screening Tool for the Assessment of…”
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Cyclin D2 gene variance and expression level in pediatric acute lymphoblastic leukemia
Published in Pediatric blood & cancer (01-12-2023)“…BackgroundCyclin D2 (CCND2) is a crucial player in cell cycle regulation. CCND2 polymorphisms contribute to cancer predisposition.ObjectivesTo evaluate the…”
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Thyroid function evaluation in pediatric nephrotic syndrome: a study in a developing country
Published in The Gazette of the Egyptian Paediatric Association (01-12-2024)“…Background In steroid-resistant nephrotic syndrome (SRNS), protracted proteinuria leads to the loss of thyroxine-binding proteins resulting in low thyroid…”
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Effect of early feeding practices and eating behaviors on body composition in primary school children
Published in World journal of pediatrics : WJP (01-09-2022)“…Background Understanding children’s feeding practices and eating behaviors is important to determine etiology of childhood obesity. This study aimed to explore…”
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Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel
Published in International journal of molecular sciences (26-08-2022)“…Dominant KCNQ1 variants are well-known for underlying cardiac arrhythmia syndromes. The two heterozygous KCNQ1 missense variants, R116L and P369L, cause an…”
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Sex assignment practice in disorders of sexual differentiation: survey results from paediatric endocrinologists in the Arab region
Published in Journal of pediatric endocrinology & metabolism : JPEM (28-01-2019)“…Background Sex assignment is a major issue in disorders of sexual differentiation (DSD). Not all conditions of DSD have clear recommendations on assignment and…”
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A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE‐1 insertion in LDLR
Published in Molecular genetics & genomic medicine (01-03-2024)“…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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BONE MINERAL DENSITY AND VITAMIN D RECEPTOR GENETIC VARIANTS IN EGYPTIAN CHILDREN WITH BETA THALASSEMIA ON VITAMIN D SUPPLEMENTATION
Published in Mediterranean journal of hematology and infectious diseases (01-01-2019)“…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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Evaluation of non-thyroidal illness syndrome in shock patients admitted to pediatric intensive care unit in a developing country
Published in European journal of pediatrics (01-02-2024)“…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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Bovine Colostrum in the Treatment of Acute Diarrhea in Children: A Double-Blinded Randomized Controlled Trial
Published in Journal of tropical pediatrics (1980) (01-02-2020)“…Abstract Objectives To evaluate the effect of bovine colostrum (BC) on the treatment of children with acute diarrhea attending the outpatient clinic. Methods…”
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Late Endocrine Disorders of Childhood Brain and Neck Cancer Survivors
Published in Indian journal of pediatrics (01-06-2023)Get full text
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Sensory Processing and Gastrointestinal Manifestations in Autism Spectrum Disorders: No Relation to Clostridium difficile
Published in Journal of molecular neuroscience (2021)“…The role of the gut microbiota in triggering autism is a rapidly emerging field of research. Gut microbiota have been incriminated because autistic children…”
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