Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nahed Mohammed Hablas"'
Autor:
Nahed Mohammed Hablas, Rasha Elshafey, Amal El-Bendary, Adel A Hagag, Lamia M. Morad, Mohamed El-Shanshory
Publikováno v:
Journal of Advances in Medicine and Medical Research. :97-109
Background: Thalassemia is a common genetic disorder associated with endocrine disorders. Iron deposition may start in the anterior pituitary gland, but clinical signs are usually not evident until puberty. Aim of the study was to evaluate pituitary
Publikováno v:
Indian J Hematol Blood Transfus
Asymmetric dimethylarginine (ADMA) level may play a role in the pathogenesis of cerebrovascular stroke in Children with Sickle Cell Anemia (SCA). To assess the plasma level of ADMA in children with SCA and its correlation to cerebral blood flow. This
Autor:
Mohamed, El-Shanshory, Nahed Mohammed, Hablas, Yasmin, Shebel, Osama, Alhadramy, Rehab, El-Tahlawi, Moutasem Salih, Aboonq, Tamer M, Soliman, Abdelhady Ragab, Abdel-Gawad, Sayed Mostafa, El Sayed, Hesham I, Abdallah, Hany Salah, Mahmoud, Hassan, El-Allaf, Samer, El-Sawy, Reda S, Yousef, Mostafa, Abu-El Naga, Reham A, Mariah, Manal Mohamed Helmy, Nabo, Mohamed, Abdel-Haleem, Ahmed Alamir, Mahmoud, Mohammad Ahmad, Hassan, Areej Hesham, Al Arabi, Abdullah Ahmed, Alnakhli, Salah Mohamed, El Sayed
Publikováno v:
Am J Blood Res
Thalassemia is a major health problem in affected children due to iron overload, increased oxidative stress, atherogenic lipid profile and tissue-damage. This study aims at investigating the cardioprotective and tissue-protective benefits of Al-hijam
Autor:
Nahed Mohammed Hablas, Hassan M. El-Asy, Ibrahim M Badraia, Amal Ezzat Abd El-Latif, Adel A Hagag
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 19:46-52
Background: Sickle Cell Disease (SCD) is characterized by defective hemoglobin synthesis, hemolytic anemia, frequent thrombosis and chronic organ damage including endocrine organs. Aim: To assess thyroid function in children with SCD in correlation a
Publikováno v:
Pediatric hematology and oncology. 36(3)
β-Thalassemia, a blood disease instigated by mutations in β-globin genes or their regulatory regions. Infectious complications, immune abnormalities and iron overload related organ damage are the chief causes of morbidity and mortality. The role of
Autor:
Hamdi H. Almaramhy, Amal Albeihany, Mohamed Attia, Hussam Baghdadi, Salah Mohamed El Sayed, Hoda Ali Ibrahim, Amr El-Dardear, Mongi Ayat, Manal Mohamed Helmy Nabo, Yasmin Shebl, Mohamed El-Shanshory, Ahmed Ragab Fakhreldin, Hany Salah Mahmoud, Nahed Mohammed Hablas
Publikováno v:
Journal of Blood Medicine
Background Thalassemia is a major health problem due to iron overload, iron deposition and oxidative stress-induced tissue damage. Here, we introduce Al-hijamah (a minor surgical excretory procedure) as a novel percutaneous iron excretion therapy. Al
Autor:
Wael El‐Feky, Samir Hassan, Mohamed El-Kashlan, Mohamed El-Sanosy, Doaa El Amrousy, Nagat S. Elshmaa, Shimaa Elrifaey, Nahed Mohammed Hablas
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Postoperative junctional ectopic tachycardia is one of the most serious arrhythmias that occur after pediatric cardiac surgery, difficult to treat and better to be prevented. Our aim was to assess the efficacy of prophylactic dexmedetomidi
Autor:
Manal Mohamed Helmy Nabo, Mohamed El-Shanshory, Sayed Moustafa, Mona Zidan, Nahed Mohammed Hablas, Rami Alharbi, Salah Mohamed El Sayed, Mongi Ayat, Mohammed Attia, Hussam Baghdadi, Samer A. El-Sawy, Momen Elshazley, Mohammed Zolaly, Reham A. Mariah, Moutasem Salih Aboonq, Ahmed Ragab Fakhreldin, Walaa Arafa, Mostafa Abu-el Naga, Hamdi H. Almaramhy
Publikováno v:
Journal of Herbal Medicine. 16:100245
Introduction Thalassemias are treated by regular blood transfusions and iron chelation therapy. Iron overload-induced oxidative stress helps the pathogenesis of thalassemia-induced anemia, atherogenesis, immune suppression and tissue damage. Nigella
Autor:
Nahed Mohammed Hablas, Ghada Abdulmomen Suliman, Ahmed Esam, Hossam Hodeib, Doaa El Amrousy, Eman Ramadan Salama
Publikováno v:
Pediatric cardiology. 38(2)
Heart failure (HF) has high morbidity and mortality in children. This study aimed to investigate the value of cardiac myosin binding protein-C (cMyBP-C) as a diagnostic and prognostic biomarker in children with heart failure. This study was a prospec