Impact of genotype on endocrinal complications in β-thalassemia patients.

Faculty Medicine Year: 4016
Type of Publication: ZU Hosted Pages:
Authors:
Journal: biomedical reports spandidos Volume:
Keywords : Impact , genotype , endocrinal complications , β-thalassemia patients.    
Abstract:
in β-thalassemia, certain mutations cause a complete absence of β-globin chain synthesis, termed β0-thalassemia, while others may allow certain β-globin production and are termed β+- or β++-thalassemia. The homozygous state results in sever
   
     
 
       

Author Related Publications

  • Tamer Hassan Mostafa, "Magnetic resonance imaging of the brain in survivors of childhood acute lymphoblastic leukemia.", spandidos publications, 2013 More
  • Tamer Hassan Mostafa, "Impact of health instructions on improving knowledge and practices of haemophilia A adolescents: a single centre experience.", HEMOPHILIA, 2014 More
  • Tamer Hassan Mostafa, "Pattern of malignant solid tumors and lymphomas in children in the east delta of Egypt: A five-year study.", sPANDIDOS PUBLICATIONS, 2014 More
  • Tamer Hassan Mostafa, "Assessment of cognitive function in children with beta-thalassemia major: a cross-sectional study.", JOURNAL OF CHILD NEUROLOGY, 2014 More
  • Tamer Hassan Mostafa, "Clinico-epidemiology of neuroblastoma in north east Egypt: A 5-year multicenter study.", SPANDIDOS PUBLICATIONS, 2015 More

Department Related Publications

  • Mohamed El Sayed Hamed, "INCIDENCE OF EARLY ARRHYTHMIAS AFTER CONGENITAL CARDIAC SURGERY", The EGYPTIAN PEDIATRIC ASSOCIATION GAZETTE, 2012 More
  • Besheer Abdallah Hassan Meawad, "Plasma neutrophil gelatinase-associated lipocalin as a marker for the prediction of worsening renal function in children hospitalized for acute heart failure", saudi journal, 2014 More
  • Wafa Fathy Mohamed Saeed, "Impact of socioeconomic status on severity and outcome of community acquired pneumonia among Egyptian children: A cohort study", Infectious Diseases of Poverty 2014, 3:14, 2014 More
  • Tamer Hassan Mostafa, "Catechol-O-methyltransferase Val158Met polymorphism and hyperactivity symptoms in Egyptian children with autism spectrum disorder.", research in developmental disabilities, 2013 More
  • Mohamed Ahmed Ahmed Mhmoud, "Electroencephalographic Abnormalities in Children with Autism اضطرابات رسم المخ في الاطفال المصابين بالتوحد", International Journal Of Child Neuropsychiatry Vol,11(1-2) 2014, 2014 More
Tweet