Peer reviewed Publications

Showing 70 items
Treatment of hepatitis B and C in children El-Shabrawi M, Hassanin F Minerva Medica 2014 Abstract 
Diagnosis and treatment of the hemolytic uremic syndrome disease spectrum in developing regions Johannes Hofer, Thomas Giner, Hesham Safouh Eminars in Thrombosis and Hemostasis 2014 Abstract 
Serum bilirubin and bilirubin/albumin ratio as predictors of bilirubin encephalopathy Iskander I, Gamaleldin R, El Houchi S, El Shenawy A, Seoud I, El Gharbawi N, Abou-Youssef H, Aravkin A,Wennberg RP Pediatrics  2014 Abstract 
A study of familial Mediterranean Fever (MEFV) gene mutations in Egyptian children with type 1 diabetes mellitus • Ghada Mohammad Anwar, • Hanan M. Fouad , • Amal Abd El-Hamid, • Faten Mahmoud, • Noha Musa, • Hala Lotfi, • Nermine Salah European Journal of Medical Genetics 2014 Abstract 
Prevalence of myocarditis in pediatric intensive care unit cases presenting with other system involvement Rady HI, Zekri H Jornal de Pediatria 2014 Abstract 
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy Halbritter J, Porath JD, Diaz KA, Braun DA, Kohl S, Chaki M, Allen SJ, Soliman NA, Hildebrandt F, Otto EA; GPN Study Group. Human Genetics 2013 Abstract 
Apolipoprotein E gene polymorphism and the risk of left ventricular dysfunction among Egyptian β-thalassemia major. El-Tagui MH, Hamdy MM, Shaheen IA, Agha H, Abd-Elfatah HA. Gene 2013 Abstract 
A 1-year randomized controlled trial of deferasirox vs deferoxamine for myocardial iron removal in β-thalassemia major (CORDELIA) 1. Dudley J. Pennell, 2. John B. Porter. 3. Antonio Piga, 4. Yongrong Lai, 5. Amal El-Beshlawy, 6. Khawla M. Belhoul, 7. Mohsen Elalfy, 8. Akif Yesilipek, 9. Yurdanur Kilinç, 10. Tomasz Lawniczek, 11. Dany Habr, 12. Marianne Weisskopf, 13. Yiyun Zhang, and 14. Yesim Aydinok, 15. on behalf of the CORDELIA study investigators Blood 2014 Full Paper 
Mutational Spectrum of the CTNS Gene in Egyptian Patients with Nephropathic Cystinosis Soliman NA, Elmonem MA, van den Heuvel L, Abdel Hamid RH, Gamal M, Bongaers I, Marie S, Levtchenko E. Journal of Inherited and Metabolic Diseases Reports 2014 Abstract 
The 6-min walk test: an independent correlate of elevated tricuspid regurgitant jetvelocity in children and young adult sickle cell patients Hala Agha, Mona El Tagui, Mona El Ghamrawy, Marwa Abdel Hady Annals of Hematology 2014 Abstract 
Study of non-organ-specific antibodies in children with genotype 4 chronic hepatitis C. Hamed ME, Alanani Kamal NM, Sherief LM, Fouad MA, Elwahab LA, Raafat N J Gastroenterol.  2013 Abstract 
Growth in infants with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: An analysis of the factors affecting height • Mona Mamdouh Hassan, Amany Ibrahim, Amina Abdel-Salam, Hamsa Huthail  The Gazette of the Egyptian Paediatric Association 2013 Abstract 
Low prevalence of cardiac siderosis in heavily iron loaded Egyptian thalassemia major patients El Beshlawy A, El Tagui M, Hamdy M, El Ghamrawy M, Azim KA, Salem D, Said F, Samir A, St Pierre T, Pennell DJ. Ann Hematol. 2013 Abstract 
MEFV mutations in egyptian children with systemic-onset juvenile idiopathic arthritis Lotfy HM, Kandil ME, Issac MS, Salah S, Ismail NA, Abdel Mawla MA Molecular Diagnosis & Therapy 2014 Abstract 
Assessment of inter-atrial, inter-ventricular, and atrio-ventricular interactions in tetralogy of Fallot patients after surgical correction. Insights from two-dimensional speckle tracking and three-dimensional echocardiography Mohamed Abd El Rahmana, Tanja Raedle-Hursta Axel Rentzscha, Hans-Joachim Schäfersa and Hashim Abdul-Khaliqa Cardiology in the Young 2014 Abstract 
Oxidant-antioxidant status in Egyptian children with sickle cell anemia: a single center based study • Mona Kamal El-Ghamrawy, • Wagdi Maurice Hanna, • Amina Abdel-Salam • Marwa M. El-Sonbaty, • Eman R. Youness, • Ahmed Adel Jornal de Pediatria 2014 Full Paper 
The link between some alleles on human leukocyte antigen system and autism in children. Mostafa GA, Shehab AA, Al-Ayadhi LY. J Neuroimmunol.  2013 Abstract 
Blood zinc levels in children hospitalized with pneumonia: • Hanaa I. Rady, Walaa A. Rabie, Heba A. Rasslan, Ahmed A. El Ayadi  Egyptian Journal of Chest Diseases and Tuberculosis 2013 Abstract 
Blood spot versus plasma chitotriosidase: a systematic clinical comparison. Elmonem MA, Ramadan DI, Issac MS, Selim LA, Elkateb SM Clin Biochem 2013 Abstract 
Predicting growth response among Egyptian prepubertal idiopathic isolated growth hormone deficient children. Salah N, Abd El Dayem SM, Fawaz L, Ibrahim M. J Pediatr Endocrinol Metab. 2013 Abstract 
A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; the SRNS Study Group, Hildebrandt F Journal of the American Society of Nephrology 2014 Abstract 
Applicability and efficacy of a model for prevention of perinatal transmission ofhepatitis B virus infection: Single center study in Egypt Hanaa M El-Karaksy, Lamiaa M Mohsen, Doa’a A Saleh, Mona S Hamdy, Noha A Yassin, Mohamed Farouk, Mohamed E Salit, and Mortada H El-Shabrawi World Journal of Gastroeneterology 2014 Full Paper 
Pattern of intravenous immunoglobulins (IVIG) use in a pediatric intensive care facility in a resource limited setting. Galal NM. Afr Health Sci. 2013  
Diagnosis of gastrointestinal basidiobolomycosis: a mini-review 1. Mortada H. El-Shabrawi, 2. Naglaa Mohamed Kamal, 3. Kerstin Kaerger and 4. Kerstin Voigt Mycoses 2014 Abstract 
Impact of an infection-control program on nurses' knowledge and attitude in pediatric intensive care units at Cairo University hospitals. Yasmine S Galal, John R Labib , Walaa A Abouelhamd  The Journal of the Egyptian Public Health Association 2013 Abstract 
Behavioral changes in Egyptian children with nephrotic syndrome. Ghobrial EE, Fahmey SS, Ahmed ME, Botrous O. Iran J Kidney Dis. 2013 Abstract 
The role of intensive phototherapy in decreasing the need for exchange transfusion in neonatal jaundice Edris AA, Ghany EA, Razek AR, Zahran AM Journal of the Pakistan Medical Association 2014 Abstract 
Burden of pediatric hepatitis C. El-Shabrawi MH, Kamal NM World J Gastroenterol 2013 Abstract 
Interleukin-18 -607C/A gene polymorphism in Egyptian asthmatic children Shaaban HH, Mohy AM, Abdel-Razek AR, Wahab AA Molecular Diagnosis & Therapy 2014 Abstract 
Detection of Mediterranean fever gene mutations in Egyptian children withinflammatory bowel disease 1. Samia Salah, 2. Mortada El-Shabrawi, 3. Hala Mohamed Lotfy, 4. Hala Fathy Shiba, 5. Maha Abou-Zekri and 6. Yomna Farag International Journal of Rheumatic Diseases 2014 Abstract 
Application of different scoring systems and their value in pediatric intensive care unit • Hanaa I. Rady, Shereen A. Mohamed, Nabil A. Mohssen, Mohamed ElBaz Egyptian Pediatric Association Gazette 2013 Abstract 
Automatic Tube Compensation versus Pressure Support Ventilation and Extubation Outcome in Children: A Randomized Controlled Study. El-Beleidy AS, Khattab AA, El-Sherbini SA, Al-Gebaly HF ISRN Pediatr 2013 Full Paper 
Adrenocortical status in infants and children with sepsis and septic shock Hanaa I. Rady, , Yasmin S. Aly, Mona Hafez, • Hafez M. Bazaraa Egyptian Pediatric Association Gazette 2014 Full Paper 
Study of thyroid function in Egyptian children with β-thalassemia major and β-thalassemia intermedia. Abdel-Razek AR1, Abdel-Salam A, El-Sonbaty MM, Youness ER J Egypt Public Health Assoc 2013 Abstract 
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA, Natarajan S, Wiggins RC, Lovric S, Chernin G, Schoeb DS, Ovunc B, Frishberg Y, Soliman NA, Fathy HM, Goebel H, Hoefele J, Weber LT, Innis JW, Faul C, Han Z, Washburn J, Antignac C, Levy S, Otto EA, Hildebrandt F. Journal of Clinical Investigation 2013 Abstract 
• Household costs of seeking outpatient care in Egyptian children with diarrhea: a cross-sectional study.  • Abeer Barakat, Eman Fawzy Halawa  The Pan African medical journal 2013 Abstract 
Decreasing intra-dialytic morbid events and assessment of dry weight in children on chronic hemodialysis using non-invasive changes in hematocrit Fadel FI, Makar SH, Eskander AE, Aon AH Saudi Journal of Kidney Diseases & Transplantation 2014 Full Paper 
Effect of bosentan therapy on ventricular and atrial function in adults with Eisenmenger syndrome. A prospective, multicenter study using conventional and Speckle tracking echocardiography Mohamed Y. Abd El Rahman, Axel Rentzsch, Philipp Scherber, Siegrun Mebus, Oliver Miera, Günther Balling, Petra Böttler, Karl-Otto Dubowy, Birgit Farahwaschy, Alfred Hager, Joachim Kreuder, Brigitte Peters, Felix Berger, Ingram Schulze-Neick, Hashim Abdul-Khaliq  Clinical Research in Cardiology 2014 Abstract 
Doppler Assessment of Renal Hemodynamic Alterations in Homozygous Sickle Cell Disease and Sickle Beta-Thalassemia Saif A, Soliman N, Abdelhamid A. Ultrasonic Imaging 2014 Abstract 
Hypertrophic cardiomyopathy: prognostic factors and survival analysis in 128 Egyptian patients El-Saiedi SA, Seliem ZS, Esmail RI Cardiology in the Young 2014 Abstract 
Oxidative stress in Egyptian hemodialysis children Ghobrial EE, Mahfouz NN, Fathy GA, Elwakkad AA, Sebaii HM Iran J Kidney Dis 2013 Abstract 
Vitamin D deficiency in Egyptian mothers and their neonates and possible related factors. El Rifai NM, Abdel Moety GA, Gaafar HM, Hamed DA. J Matern Fetal Neonatal Med. 2013 Abstract 
Response to hydroxycarbamide in pediatric β thalassemia intermedia: 8 years follow-up in Egypt Amal El-Beshlawy, Mona El-Ghamrawy, Mona Abou EL-Ela,Fadwa Said, Sonia Adolf, Abdel-Rahman Ahmed Abdel-Razek, Rania Ismail Magdy, Amina Abdel-Salam Annals of Hematology 2014 Abstract 
Study of primary IGF-1 deficiency in Egyptian children with idiopathic shor Anwar GM, Kandeel WA, Mandour IA, Kamal AN. Horm Res Paediatr 2013 Abstract 
• Study of Primary IGF-1 Deficiency in Egyptian Children with Idiopathic Short Stature.  • Ghada M Anwar, Wafaa A Kandeel, Iman A Mandour, Ayat N Kamal  Hormone Research in Paediatrics 2013 Abstract 
Prevalence and Distribution of Iron Overload in Patients with Transfusion-dependentAnemias Differs across Geographic Regions: Results from the CORDELIA Study 1. Yesim Aydinok, 2. John B Porter, 3. Antonio Piga, 4. Mohsen Elalfy, 5. Amal El-Beshlawy, 6. Yurdanur Kilinç, 7. Vip Viprakasit, 8. Akif Yesilipek,  European Journal of Hematology 2014 Abstract 
Surgical complications and graft function following live-donor extraperitoneal renal transplantation in children 20 kg or less ElSheemy MS, Shouman AM, Shoukry AI, Soaida S, Salah DM, Yousef AM, Morsi HA, Fadel FI, Sadek SZ Pediatric Urology 2014 Abstract 
A prospective study on hyperglycemia and retinopathy of prematurity Mohsen L, Abou-Alam M, El-Dib M, Labib M, Elsada M, Aly H Journal of Perinatology 2014 Abstract 
• CD 4+ CD 25+ cells in type 1 diabetic patients with other autoimmune manifestations  • Dalia Abdelaziz, Mona Hafez, Nermeen Galal, Safa Meshaal, Aisha EL marsafy Journal of Advanced Research 2013 Abstract 
Blood spot versus plasma chitotriosidase: a systematic clinical comparison Elmonem MA, Ramadan DI, Issac MS, Selim LA, Elkateb SM Clinical Biochemistry 2014 Abstract 
Neurocognitive functions and behavioral profiles in children with nephropathic cystinosis Reham Aly, Samuel Makar, Azza El Bakri, Neveen A Soliman Saudi Journal of Kidney Diseases & Transplantation 2014 Full Paper 
Clinical and ultrasonographical characterization of childhood cystic kidney diseases in Egypt Soliman NA, Nabhan MM, Bazaraa HM, Badr AM, Shaheen M. Renal Failure 2014 Abstract 
Assessment of coagulation and fibrinolysis in children with chronic liver disease. El-Sayed R, El-Karaksy H, El-Raziky M, El-Hawary M, El Koofy N, Helmy H, Fahmy M. Blood Coagul Fibrinolysis. 2013 Abstract 
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome Lovric S, Fang H, Vega-Warner V, Sadowski CE, Gee HY, Halbritter J, Ashraf S, Saisawat P, Soliman NA, Kari JA, Otto EA, Hildebrandt F; Nephrotic Syndrome Study Group. Clinical Journal of American Society of Nephrology 2014 Abstract 
Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, and GSTP1) inEgyptian pediatric patients with sickle cell disease Hala Fathy Shiba, Mona Kamal El-Ghamrawy, Iman Abd El-Mohsen Shaheen, Rasha Abd El-Ghani Ali , and Somaia Mohammed Mousa Pediatric and Developmental Pathology 2014 Abstract 
Pregnancy outcome and the effect of maternal nutritional status. Abdel-Raoufabdel-Aziz Afifi R, Ali DK, Talkhan HM. J Egypt Soc Parasitol 2013 Abstract 
• Natural History and Response to Treatment of HCV Infection Among Egyptian Survivors of Childhood Malignancy.  • Mona Saeed El-Raziky, Eman Fawzy Halawa, Iman Hassan Draz, Mona Samir Ali Pediatric hematology and oncology 2013 Abstract 
Permanent cardiac pacing in pediatric patients. Lotfy W, Hegazy R, AbdElAziz O, Sobhy R, Hasanein H, Shaltout F. Pediatr Cardiol 2013 Abstract 
Nephropathic cystinosis in a developing country: the Egyptian experience Soliman NA, Bazaraa HM, Abdel Hamid RH, Badawi N. Saudi Journal of Kidney Diseases & Transplantation 2013 Abstract 
Frequency of Helicobacter pylori infection among Egyptian children presenting with gastrointestinal manifestations. Abu-Zekry MA, E S Hashem M, Ali AA, Mohamed IS J Egypt Public Health Assoc. 2013 Abstract 
Commentary on: The optimal Dose of Ribavirin for Chronic Hepatitis C: From Literature Evidence to Clinical Practice. El-Shabrawi M, Isa M. Hepat Mon 2013 Abstract 
Altered Right Ventricular Function in the Long-Term Follow-up Evaluation of Patients After Delayed Aortic Reimplantation of the Anomalous Left Coronary Artery From the Pulmonary Artery Rita Schuck, Mohamed Y. Abd El Rahman, Axel Rentzsch, Wei Hui, Yuguo Weng, Vladimir Alexi-Meskishvili, Peter E. Lange, Felix Berger, Hashim Abdul-Khaliq Pediatric Cardiology 2014 Abstract 
Glycogen storage disease type III in Egyptian children: a single centre clinico-laboratory study El-Karaksy H, Anwar G, El-Raziky M, Mogahed E, Fateen E, Gouda A, El-Mougy F, El-Hennawy A Arab Journal of Gastroenterology 2014 Abstract 
Regional Analysis of Longitudinal Systolic Function of the Right Ventricle After Corrective Surgery of Tetralogy of Fallot Using Myocardial Isovolumetric Acceleration Index Mohamed Y. Abd El Rahman, Wei Hui, Rita Schuck, Axel Rentzsch, Felix Berger, M. Gutberlet, Hashim Abdul-Khaliq Pediatric Cardiology 2013 Abstract 
Egyptian growth hormone deficient patients: demographic, auxological characterization and response to growth hormone therapy. Salah N, Abd El Dayem SM, El Mogy F, Amin M, Ibrahim M. J Pediatr Endocrinol Metab. 2013 Abstract 
Entomophthoromycosis: a challenging emerging disease 1. Mortada H. F. El-Shabrawi, 2. Heba Arnaout, 3. Lamiaa Madkour and 4. Naglaa Mohamed Kamal Mycoses 2014 Abstract 
Blood transfusion among thalassemia patients: A single Egyptian center experience. Ragab LA, Hamdy MM, Shaheen IA, Yassin RN. Asian J Transfus Sci. 2013 Abstract 
Apolipoprotein E gene polymorphism and the risk of left ventricular dysfunction among Egyptian β-thalassemia major • Mona H. El-Tagui, • Mona M. Hamdy, • Iman A. Shaheen , • Hala Agha, • Hoda A. Abd-Elfatah Gene 2014 Abstract 
Exome sequencing links corticospinal motor neuron disease to commonneurodegenerative disorders Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Matan Hofree, Jennifer L. Silhavy, Andrew D. Heiberg, Mostafa Abdellateef, Basak Rosti, Eric Scott, Lobna Mansour, Amira Masri, Hulya Kayserili, Jumana Y. Al-Aama, Ghada M. H. Abdel-Salam, Ariana Karminejad, Majdi Kara, Bulent Kara, Bita Bozorgmehri, Tawfeg Ben-Omran, Faezeh Mojahedi, Iman Gamal El Din Mahmoud, Naima Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Laure Raymond, Sylvie Forlani, Massimo Mascaro, Laila Selim, Nabil Shehata, Nasir Al-Allawi, P.S. Bindu, Matloob Azam, Murat Gunel, Ahmet Caglayan, Kaya Bilguvar, Aslihan Tolun, Mahmoud Y. Issa, Jana Schroth, Emily G. Spencer,1 Rasim O. Rosti, Naiara Akizu, Keith K. Vaux, Anide Johansen, Alice A. Koh, Hisham Megahed, Alexandra Durr, Alexis Brice, Giovanni Stevanin, Stacy B. Gabriel, Trey Ideker and Joseph G. Gleeson Science 2014 Full Paper 
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract Hwang DY, Dworschak GC, Kohl S, Saisawat P, Vivante A, Hilger AC, Reutter HM, Soliman NA, Bogdanovic R, Kehinde EO, Tasic V, Hildebrandt F Kidney International 2014 Abstract 
Showing 70 items