Mortality Rate in Mechanically Ventilated Neonates: A Developing Country Experience

by Wesam A. Mokhtar, Laila Sherief, Naglaa M. Kamal, Sherief Kamel
Published 2021-04-01

Favorable response to carbamazepine therapy in genetically proven myoclonus-dystonia child

by Mohammed F. Aljabri, Naglaa M. Kamal, Abdulrhman Alghamdi, Hamdan Alghamdi, Naif Alomairi
Published 2021-02-01

Sjogren–Larsson Syndrome: A case series of five members from an extended family with a novel mutation

by Kamel T. Abidi, Naglaa M. Kamal, Ayman A. Bakkar A., Maram Alotaibi, Haifa Asseri, Kawthar A. Bokari
Published 2020-11-01

Study of non-organ-specific antibodies in children with Genotype 4 chronic Hepatitis C

by Mohammed E Hamed, Naglaa M Kamal Alanani, Laila M Sherief, Mohammed A Fouad, Lamiaa A Elwahab, Nermin Raafat
Published 2013-01-01

Outpatient blind percutaneous liver biopsy in infants and children: Is it safe?

by Mortada H El-Shabrawi, Hanaa M El-Karaksy, Sawsan H Okahsa, Naglaa M Kamal, Gamal El-Batran, Khaled A Badr
Published 2012-01-01

Knowledge of Neonatal Hyperbilirubinemia Among Primary Health Care Physicians: A Single-Center Experience

by Mostafa A Mostafa, Naglaa M Kamal, Sherif Eltaher, Yahia Hamed, Hany Abdelaziz, Walid Abdelghany, Efat Aser, Eman Fawzy, Laila M Sherief
Published 2019-02-01

NT-proBNP as Early Marker of Subclinical Late Cardiotoxicity after Doxorubicin Therapy and Mediastinal Irradiation in Childhood Cancer Survivors

by Amal Zidan, Laila M. Sherief, Amera El-sheikh, Safaa H. Saleh, Doaa A. Shahbah, Naglaa M. Kamal, Hanan S. Sherbiny, Heba Ahmad
Published 2015-01-01

Huge Non-parasitic Mesothelial Splenic Cyst in a Child: A Case Report and Literature Review

by Imed Krichen, Kais Maazoun, Murad Kitar, Naglaa M Kamal, Ubaidullah Khan, Mostafa YL Khalif, Rasha A, Haifa Assiri, Kawthar Abdulrhim Bokari
Published 2021-06-01

CMV, B and C hepatitis among multi-transfused hereditary hemolytic Anemia children: an updated Egyptian experience

by Laila M. Sherief, Seham M. Ragab, Mohamed A. Helwa, Naglaa M. Kamal, Mona R. Afify, Rasha T. S. Mohammed, Ghada Abd Elmoniem Mokhtar, Hanan S. Sherbiny
Published 2021-05-01

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

by Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli, Naglaa M. Kamal, Naglaa M. Kamal, Ahmed N. Sahly, Ahmed N. Sahly, Hadeel A. Alsufyani, Arif Mohammed, Aftab Ahmad, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Ramu Elango, Ramu Elango
Published 2021-04-01

Factor VIII inhibitor development in Egyptian hemophilia patients: does intron 22 inversion mutation play a role?

by Laila M. Sherief, Osama A. Gaber, Hala Mosaad Youssef, Hanan S. Sherbiny, Wesam a Mokhtar, Asmaa A. A. Ali, Naglaa M. Kamal, Yehia H. Abdel Maksoud
Published 2020-09-01

Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients

by Naglaa M. Kamal, Ahmed N. Sahly, Babajan Banaganapalli, Omran M. Rashidi, Preetha J. Shetty, Jumana Y. Al-Aama, Noor A. Shaik, Ramu Elango, Omar I. Saadah
Published 2020-01-01

Pilot study of classic galactosemia: Neurodevelopmental impact and other complications urge neonatal screening in Egypt

by Magd A. Kotb, Lobna Mansour, Christine William Shaker Basanti, Wael El Garf, Ghada I.Z. Ali, Sally T. Mostafa El Sorogy, Inas E.M. Kamel, Naglaa M Kamal
Published 2018-07-01

Nutritional Biomarkers in Children and Adolescents with Beta-Thalassemia-Major: An Egyptian Center Experience

by Laila M. Sherief, Sanaa M. Abd El-Salam, Naglaa M. Kamal, Osama El safy, Mohamed A. A. Almalky, Seham F. Azab, Hemat M. Morsy, Amal F. Gharieb
Published 2014-01-01

Persistent Hypertransaminasemia Uncovered Occult Limb-Girdle-Muscle Dystrophy-Type-2C in a Saudi Child

by Naglaa M. Kamal, Hamed A. Alghamdi, Abdulrahman Halabi, Abdullah O. Alharbi, Muhammad Rafique, Kamel Abidi, Mortada H.H. El-Shabrawi, Ayman E. Eskander, Hala Mansour, Laila M. Sherief
Published 2018-03-01

Genetic polymorphism of vitamin D receptors and plasminogen activator inhibitor‐1 and osteonecrosis risk in childhood acute lymphoblastic leukemia

by Laila M. Sherief, Mohamed Beshir, Nermin Raafat, Elhamy R. Abdelkhalek, Wesam A. Mokhtar, Khaled M. Elgerby, Basma K. Soliman, Hosam E. Salah, Ghada A. Mokhtar, Naglaa M. Kamal, Heba ELsayed, Marwa Zakaria
Published 2021-07-01

Serum endocan and endothelial dysfunction in childhood acute lymphoblastic leukemia survivors: a tertiary center experience

by Laila M. Sherief, Elhamy R. Abd El-khalek, Ibrahim A. Libda, Osama A. Gaber, Naglaa M. Kamal, Basma K. Soliman, Wesam A. Mokhtar, Ghada A. Mokhtar, Hosam E. Salah, Gehad M. Kamar, Marwa Zakaria
Published 2021-05-01

Serum Neuron-specific Enolase and S100 Calcium-binding Protein B in Pediatric Diabetic Ketoacidosis

by Hatem Hamed Elshorbagy, Naglaa Fathy Barseem, Akram Elshafey Elsadek, Ashraf Hamed Al-shokary, Yehia Hamed Abdel Maksoud, Sameh Elsayed Abdulsamea, Iman M. Talaat, Hany Abdelaziz Suliman, Naglaa M. Kamal, Waleed E. Abdelghani, Sanaa Mohammed Azab, Dalia Mohamed Nour El Din
Published 2019-12-01

Hepatic Injury in Neonates with Perinatal Asphyxia

by Akram Elshafey Elsadek MD, Naglaa FathyBarseem MD, Hany Abdelaziz Suliman MD, Hatem Hamed Elshorbagy MD, Naglaa M. Kamal MD, Iman M. Talaat MD, Ashraf Hamed Al-shokary MD, Yehia Hamed Abdel Maksoud MD, Asmaa Obada Ibrahim MD, Ahmed Mahmoud Attia, Waleed Abdellateef Abdelhalim MD, Waleed Elsayed Abdelghani MD
Published 2021-01-01