Long Term Follow up of Children with Hepatic Forms of Glycogen Storage Disease متابعة طويلة المدى للأطفال الذين يعانون من اختلال تخزين الجليكوجين (الأنواع الكبدية)
Gomaa Gaballah Mosaed جمعة جاب الله مساعد;
Abstract
Glycogen Storage diseases (GSDs) are inherited disorders in which the concentration and / or molecular structure of glycogen is abnormal. Liver and skeletal muscles are the tissues most severely affected but heart, kidney, bones, and brain may be involved
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| Title | Long Term Follow up of Children with Hepatic Forms of Glycogen Storage Disease متابعة طويلة المدى للأطفال الذين يعانون من اختلال تخزين الجليكوجين (الأنواع الكبدية) | Authors | Gomaa Gaballah Mosaed جمعة جاب الله مساعد | Keywords | Long Term Follow up of Children with Hepatic Forms of Glycogen Storage Disease متابعة طويلة المدى للأطفال الذين يعانون من اختلال تخزين الجليكوجين (الأنواع الكبدية) | Issue Date | 2009 | Description | Glycogen Storage diseases (GSDs) are inherited disorders in which the concentration and / or molecular structure of glycogen is abnormal. Liver and skeletal muscles are the tissues most severely affected but heart, kidney, bones, and brain may be involved |
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