HT2A receptor gene polymorphisms with gastrointestinal disorders in Egyptian children with autistic disorder

Faculty Medicine Year: 2015
Type of Publication: ZU Hosted Pages:
Authors:
Ashgan Abdallah Abdelaal
Journal: Research in Developmental Disabilities 36 (2015) 485–490 Research in Developmental Disabilities 36 (2015) 485–490 Volume:
Keywords : HT2A receptor gene polymorphisms with gastrointestinal    
Abstract:
مقدمه البحث كثيرا ما ذكرت اضطرابات الجهاز الهضمي في الأطفال الذين يعانون من اضطرابات طيف التوحد وهناك أدلة متزايدة تشير إلى أنه قد يكون هناك ارتباط وراثي لحدوث اضطرابات الجهاز الهضمي مع مرض التوحد الهدف الهدف من الدراسه هو التحقيق
   
     
 
       

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  • Ashgan Abdallah Abdelaal, "ROLE OF NEUROINAGING IN REWRRENT BACTERIAL MENIGITIS", لايوجد, 1900 More
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  • Ashgan Abdallah Abdelaal, "Intrleukin-12 levels in Egyptian children with type 1 diabetes mellitus", Egypt J Pediatr Allergy Immunol 2013;11(1):41-45., 2013 More
  • Ashgan Abdallah Abdelaal, "Trace elements and oxidative stress in children with type 1 diabetes mellitus", Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy 2018:11 1–8. PubMed Q1- SJR:1.53, 2018 More
  • Ashgan Abdallah Abdelaal, "Vitamin D status and vitamin D receptor gene polymorphisms and susceptibility to type 1 diabetes in Egyptian children", Gene 536 (2), 430-434 ., 2014 More

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