Peer reviewed Publications
| Publications | Authors | Journal | Year | Link |
|---|---|---|---|---|
| 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 |
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