Search Results - "Rabie Walaa"

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  1. 1

    Fabrication and characterization of novel biocomposite based on Sargassum vulgare for controlling sugar beet root diseases by Abdelwahab, Noha, Rabie, Walaa, Mohamed, Fatma

    “…Background Safe food free from diseases is the world's goal. Excessive usage of chemical fungicides is considered the most important danger for the climate…”
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  2. 2

    Identification of insulin gene variants in neonatal diabetes by Gohar, Nadida A., Rabie, Walaa A., Sharaf, Sahar A., Elsharkawy, Marwa M., Mira, Marwa F., Tolba, Aisha O., Aly, Hany

    “…Objectives: Permanent neonatal diabetes (PNDM) is caused by mutations in the genes responsible for the synthesis of different proteins that are important for…”
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  3. 3

    Initial Response and Outcome of Critically Ill Children With Guillain Barre' Syndrome by Bazaraa, Hafez M., Rady, Hanaa I., Mohamed, Shereen A., Rabie, Walaa A., ElAnwar, Noha H.

    Published in Frontiers in pediatrics (18-09-2019)
    “…Background: Guillain-Barre syndrome is the most common cause of acute flaccid paralysis worldwide since the eradication of poliomyelitis. Severe cases may…”
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  4. 4

    Birth Weight, Insulin Resistance, and Blood Pressure in Late Preterm Infants by Aly, Hany, Soliman, Reem M, El-Dib, Mohamed, Fawzy, Enas M, Badawi, Nora E, Rabie, Walaa A, Elbadawi, Ayman A

    Published in American journal of perinatology (01-07-2015)
    “…This study aims to compare insulin sensitivity, lipid profile, and blood pressure in late preterm infants born at appropriate for gestational age (AGA) and…”
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  5. 5

    Association of serotonin transporter gene (5HTT) polymorphism and juvenile myoclonic epilepsy: a case–control study by Esmail, Eman H., Labib, Dalia M., Rabie, Walaa A.

    Published in Acta neurologica Belgica (01-09-2015)
    “…Serotonin levels might alter susceptibility to seizures. Serotonin transporter (5HTT) gene polymorphisms were found to be associated with some forms of…”
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  6. 6

    Selenium and Vitamin E as antioxidants in chronic hemolytic anemia: Are they deficient? A case-control study in a group of Egyptian children by Hamdy, Mona M., Mosallam, Dalia S., Jamal, Alaa M., Rabie, Walaa A.

    Published in Journal of advanced research (01-11-2015)
    “…Accelerated oxidative damage is one of the hallmarks in both sickle cell disease (SCD) and thalassemia major (TM). A decreased antioxidant level is found in…”
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  7. 7

    Human surfactant proteins A2 (SP-A2) and B (SP-B) genes as determinants of respiratory distress syndrome by Abuelhamed, Walaa A., Zeidan, Nancy, Shahin, Walaa A., Rizk, Hoda I., Rabie, Walaa A.

    Published in Indian pediatrics (01-05-2015)
    “…Objective To study the relationship between SP-A2 and SP-B gene polymorphisms and respiratory distress syndrome in preterm neonates. Design Cross-sectional…”
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  8. 8

    Zinc Supplementation Improves Nocturnal Asthma Symptoms by Iman Abdelaziz, Magd Ahmed Kotb, Noha Adel Yassin, Walaa Ahmed Rabie, Alsayed Fathy Alsayed, Dina Hossam Hamed

    Published in Pediatric Sciences Journal (01-01-2022)
    “…Background: Treatment of bronchial asthma aims to control the symptoms of bronchoconstriction and disease modification. Zinc influences bradykinin that…”
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  9. 9

    The effect of high fat dietary modification and nutritional status on the outcome of critically ill ventilated children: single-center study by El Koofy, Nehal Mohamed, Rady, Hanaa Ibrahim, Abdallah, Shrouk Moataz, Bazaraa, Hafez Mahmoud, Rabie, Walaa Ahmed, El-Ayadi, Ahmed Ali

    Published in Korean journal of pediatrics (2019)
    “…Background: Ventilator dependency constitutes a major problem in the intensive care setting. Malnutrition is considered a major determinant of extubation…”
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  10. 10

    Aberrant p16INK4A methylation: Relation to viral related chronic liver disease and hepatocellular carcinoma by El-Mougy, Fatma A., Youssef, Mohammed M., Omran, Dalia A., Sharaf, Sahar A., El-Sayed, Hany H., Rabie, Walaa A., Mohamed, Elghobary A., Elghobary, Hany A.

    Published in South Asian journal of cancer (01-01-2014)
    “…Abstract Background: Hepatocellular carcinoma (HCC) is currently the fifth most common solid tumor worldwide and the third leading cause of cancer related…”
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  11. 11

    The effect of high fat dietary modification and nutritional status on the outcome of critically ill ventilated children: single-center study by El Koofy, Nehal Mohamed, Rady, Hanaa Ibrahim, Abdallah, Shrouk Moataz, Bazaraa, Hafez Mahmoud, Rabie, Walaa Ahmed, El-Ayadi, Ahmed Ali

    Published in Clinical and experimental pediatrics (01-09-2019)
    “…Ventilator dependency constitutes a major problem in the intensive care setting. Malnutrition is considered a major determinant of extubation failure, however,…”
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  12. 12

    Maternal urinary cell free fetal DNA in relation to gestational age by Shaban, Mona Mohamed, Salah Eldin, Noha Mohamed, Kandil, Hisham Omar, Aly Hassan, Zeinab, Rabie, Walaa A., Elgarf, Wael, Talaat Elrayes, Mohamed

    Published in Middle East Fertility Society journal (01-12-2016)
    “…Objectives: To evaluate the presence of cell-free fetal DNA in the maternal urine in relation to gestational age as a potential source for non-invasive…”
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  13. 13

    Blood zinc levels in children hospitalized with pneumonia: A cross sectional study by Hanaa I. Rady, Walaa A. Rabie, Heba A. Rasslan, Ahmed A. El Ayadi

    “…Background: Recent works have provided conflicting evidence on the role of zinc in acute lower respiratory infection (ALRI). Objective: We aimed to study the…”
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  14. 14

    Heat stress as an innovative approach to enhance the antioxidant production in Pseudooceanicola and Bacillus isolates by Hassan, Abdelrahim H. A., Hozzein, Wael N., Mousa, Ahmed S. M., Rabie, Walaa, Alkhalifah, Dalal Hussien M., Selim, Samy, AbdElgawad, Hamada

    Published in Scientific reports (15-09-2020)
    “…It is well known that the quality and quantity of bioactive metabolites in plants and microorganisms are affected by environmental factors. We applied heat…”
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  15. 15

    COVID-19 in children ranging from asymptomatic to a multi-system inflammatory disease: A single-center study by Shahin, Walaa, Rabie, Walaa, Alyossof, Osama, Alasiri, Mohammed, Alfaki, Mohamed, Mahmoud, Elamin, Hijazi, Muwaffak, Faraidi, Huda El, Alahmari, Hassan

    Published in Saudi medical journal (01-03-2021)
    “…To identify clinical and laboratory characteristics of the Saudi children with confirmed COVID-19. Eighty-eight children (0-14 years) with COVID-19 who were…”
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  16. 16

    COVID-19 in children ranging from asymptomatic to a multi-system inflammatory disease by Shahin Walaa, Rabie Walaa, Alyossof Osama, Alasiri Mohammed, Alfaki Mohamed, Elamin, Mahmoud, Hijazi Muwaffak, Faraidi, Huda El, Alahmari Hassan

    Published in Saudi medical journal (01-03-2021)
    “…Objectives:To identify clinical and laboratory characteristics of the Saudi children with confirmed COVID-19.Methods:Eighty-eight children (0-14 years) with…”
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  17. 17

    Genetic and Biochemical Predictors of Neonatal Bronchopulmonary Dysplasia by Abdellatif, May A.K., Eyada, Eman, Rabie, Walaa, Abdelaziz, Azza, Shahin, Walaa

    “…Abstract Bronchopulmonary dysplasia (BPD) is a common complication of prematurity with a multifactorial etiology, influenced by both genetic susceptibility and…”
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  18. 18

    Erythrocyte Complement Receptor 1 Gene Polymorphisms and Neonatal Respiratory Distress Syndrome by Rabie, Walaa, Al-Taweel, Ahmed, Abuelhamd, Walaa A., Shahin, Walaa, Nazeer, Marian, Aly, Hany

    “…Abstract To evaluate the role of erythrocyte complement receptor 1 ( ECR1 ) gene in the predisposition to respiratory distress syndrome (RDS), we studied 50…”
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  19. 19

    Association of the luteinizing hormone/choriogonadotropin receptor gene polymorphism with polycystic ovary syndrome by Bassiouny, Yasmin Ahmed, Rabie, Walaa Ahmed, Hassan, Ayman Ahmed, Darwish, Rania Kamal

    Published in Gynecological endocrinology (01-06-2014)
    “…Abstract This study aimed at evaluating possible associations of the single nucleotide polymorphism (SNP) in luteinizing hormone/choriogonadotropin receptor…”
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  20. 20

    Genetic variants of Pompe disease among a sample of Egyptian pediatric patients by Darwish, Rania K., Rabie, Walaa A., El Abd, Dina M., Selim, Laila A., Seliem, Zeinab S., Lotfy, Sarah A., Mehaney, Dina A.

    Published in Gene reports (01-06-2022)
    “…Pompe disease is an autosomal recessive disorder initiated by the deficiency of lysosomal acid α-glucosidase enzyme (GAA) due to disease associated variants of…”
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