Mitochondrial diseases in pediatrics / Abd El azeem Abdallah Abd El azeem ; supervised Sherief Wali Hammed , Mohamed Hussein Mebed , Ghada Mohamed Anour
Language: Eng Publication details: Cairo : Abd El azeem Abdallah Abd El azeem , 2006Description: 101p : ill ; 30cmSubject(s): Available additional physical forms:- Issued also as CD
| Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
|---|---|---|---|---|---|---|---|
Thesis
|
قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.M.Sc.2006.Ab.M. (Browse shelf(Opens below)) | Not for loan | 01010110045648000 | ||
CD - Rom
|
مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.M.Sc.2006.Ab.M. (Browse shelf(Opens below)) | 45648.CD | Not for loan | 01020110045648000 |
Browsing المكتبة المركزبة الجديدة - جامعة القاهرة shelves Close shelf browser (Hides shelf browser)
| No cover image available | No cover image available | No cover image available | No cover image available | No cover image available | No cover image available | No cover image available | ||
| Cai01.11.28.M.Sc.2005.Sa.P. Prevalence of glucose intolerance in multitransfused children with B - thalassemia major / | Cai01.11.28.M.Sc.2005.Sh.G. Gastroesophageal refiux versus Cow milk allergy in persistent vomiting in Egyptian children / | Cai01.11.28.M.Sc.2005.Sh.G. Gastroesophageal refiux versus Cow milk allergy in persistent vomiting in Egyptian children / | Cai01.11.28.M.Sc.2006.Ab.M. Mitochondrial diseases in pediatrics / | Cai01.11.28.M.Sc.2006.Ab.M. Mitochondrial diseases in pediatrics / | Cai01.11.28.M.Sc.2006.Ab.R The role of genetic factors in the etiology of autistic disorder / | Cai01.11.28.M.Sc.2006.Ab.R The role of genetic factors in the etiology of autistic disorder / |
Thesis (M.Sc.) - Cairo University - Faculty Of Medicine - Department Of Pediatrics
Mitochondrial disease can result from either nuclear DNA mutation (mendelian inheritance) or mt DNA mutations (matemal inheritance) In general , when the clinical presentation is in childhood , the patient will be short statured and the course of the disease will be more severeCertain features may be in common , egsensorineural hearing loss , dementia , neuropathies , glucose intolerance elevated serum and CSF lactic acidRed fibers (RREs) on muscle biopsy are of great significance
Issued also as CD
There are no comments on this title.