28 results on '"Megahed, Hisham"'
Search Results
2. Supplementary Data from Rapid Diagnosis of Medulloblastoma Molecular Subgroups
3. Diagnostic approach to cerebellar disorders amongst Egyptian children
4. The potential impact of CYP2D6 (*2/*4/*10) gene variants among Egyptian epileptic children: A preliminary study
5. Biallelic loss of EMC10 leads to mild to severe intellectual disability
6. Serum homocysteine, lipid profile and BMI as atherosclerotic risk factors in children with numerical chromosomal aberrations
7. Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients
8. Emm : un nouveau système de groupe sanguin associé à des troubles neurodéveloppementaux
9. Serum Homocysteine, Lipid Profile and BMI as Atherosclerotic Risk Factors in Children with Numerical Chromosomal Aberrations
10. Association of GSTP1 p.Ile105Val (rs1695, c.313A > G) Variant with the Risk of Breast Carcinoma among Egyptian Women
11. Chemerin as a Diagnostic Marker for Fmf in Egyptian Patients
12. Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders
13. Clinical Implications of S100A12 and Resolvin D1 Serum Levels, and Related Genes in Children with Familial Mediterranean Fever
14. Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
15. Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration
16. Risk Factors for Epilepsy in Developmentally Delayed Egyptian Children with Peri-Ventricular Leukomalacia
17. Non Radiological Features in Relation to Cognitive Aspects of Tuberous Sclerosis Complex in Egyptian Patients
18. Cardiac Involvement in Spinal Muscular Atrophy
19. Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population
20. Targeted treatment of tuberous sclerosis complex in Egyptian children
21. Correlation between clinical features and MECP2 gene mutations in patients with Rett syndrome
22. Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
23. DNA methylation profiling of medulloblastoma allows robust subclassification and improved outcome prediction using formalin-fixed biopsies
24. MYC family amplification and clinical risk-factors interact to predict an extremely poor prognosis in childhood medulloblastoma
25. TP53 Mutations in Favorable-Risk Wnt/Wingless-Subtype Medulloblastomas
26. Definition of Disease-Risk Stratification Groups in Childhood Medulloblastoma Using Combined Clinical, Pathologic, and Molecular Variables
27. Abstract 3442: TP53 mutations in favorable risk WNT subtype medulloblastomas
28. Rapid Diagnosis of Medulloblastoma Molecular Subgroups
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