All Stories

  1. Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families
  2. Genetic and Epigenetic Regulation of MEFV Gene and Their Impact on Clinical Outcome in Auto-Inflammatory Familial Mediterranean Fever Patients
  3. The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome
  4. BDNF as a potential predictive biomarker for patients with pediatric cerebral palsy
  5. Multiplex ligation-dependent probe amplification versus fluorescent in situ hybridization for screening RB1 copy number variations in Egyptian patients with retinoblastoma
  6. Serum homocysteine, lipid profile and BMI as atherosclerotic risk factors in children with numerical chromosomal aberrations
  7. Health-related quality of life in Egyptian patients with familial Mediterranean fever
  8. Differential Expression of micro RNAs and their Association with the Inflammatory Markers in Familial Mediterranean Fever Patients
  9. Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease
  10. Serum Homocysteine, Lipid Profile and BMI as Atherosclerotic Risk Factors in Children with Numerical Chromosomal Aberrations
  11. Epigenetics and familial mediterranean fever
  12. The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women
  13. Clinical Implications of S100A12 and Resolvin D1 Serum Levels, and Related Genes in Children with Familial Mediterranean Fever
  14. Clinical, Biochemical, and Molecular Characterization of Metachromatic Leukodystrophy Among Egyptian Pediatric Patients: Expansion of the ARSA Mutational Spectrum
  15. Inflammatory and endothelial dysfunction indices among Egyptian females with obesity classes I–III
  16. Carotid intima-media thickness, lipid profile, serum amyloid A and vitamin D status in children with familial Mediterranean fever
  17. Clinical and cytogenomic characterization of de novo trisomy 9 mosaicism in an Egyptian family: phenotype/karyotype correlation
  18. DNA Damage and Neutrophil Elastase in Children with Prader-Willi Syndrome
  19. Mutation in the SLC29A3 Gene in an Egyptian Patient with H Syndrome: A Case Report and Review of Literature
  20. Early Detection and Management of Prader-Willi Syndrome in Egyptian Patients
  21. The association of +1150A polymorphism with low GH level in isolated growth hormone deficiency (IGHD) patients
  22. Apoptosis, reactive oxygen species and DNA damage in Familial Mediterranean Fever patients
  23. Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation
  24. Assessment of physical growth, some oxidative stress biomarkers and vitamin D status in children with Familial Mediterranean Fever
  25. Screening of the most common MEFV mutations in a large cohort of Egyptian patients with Familial Mediterranean fever
  26. Evaluation of DNA damage profile in obese women and its association to risk of metabolic syndrome, polycystic ovary syndrome and recurrent preeclampsia
  27. Assessment of DNA damage in obese premenopausal women with metabolic syndrome
  28. Immunological Evaluation in Patients with Familial Mediterranean fever
  29. Association of vitamin D receptor gene polymorphism (VDR) with vitamin D deficiency, metabolic and inflammatory markers in Egyptian obese women
  30. Association of the Pro12Ala Polymorphism with the Metabolic Parameters in Women with Polycystic Ovary Syndrome
  31. Aicardi-Goutières syndrome: unusual neuro-radiological manifestations
  32. Registry of ocular anomalies among patients with genetic disorders attending the clinical genetics department at the National Research Center in Egypt
  33. Coenzyme Q10 and pro-inflammatory markers in children with Down syndrome: clinical and biochemical aspects
  34. Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients
  35. Mercury toxicity and DNA damage in patients with Down syndrome
  36. Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype
  37. Cross-sectional analysis of long bones in a sample of ancient Egyptians
  38. Behavioral problems, biochemical, and anthropometric characteristics of patients with Prader–Willi syndrome
  39. The role of H. pylori infection in gall bladder cancer: clinicopathological study
  40. Oxidative stress -a phenotypic hallmark of Fanconi anemia and Down syndrome: The effect of antioxidants
  41. Lipocalin-2 is an inflammatory biomarker associated with metabolic abnormalities in Egyptian obese children
  42. Indicators of the metabolic syndrome in obese adolescents
  43. Detection and Quantification of Free Radicals in Peroxisomal Disorders: A Comparative Study with Oxidative Stress Parameters
  44. Association of serum paraoxonase enzyme activity and oxidative stress markers with dyslipidemia in obese adolescents
  45. Mutation analysis of the GJB2 and GJB6 genes in Egyptian patients with autosomal recessive sensorineural nonsyndromic hearing loss
  46. Screening for common mutations in four FANCA gene exons in Egyptian Fanconi anemia patients
  47. Assessment of DNA Damage and Oxidative stress in Down syndrome
  48. Osteoporosis in Chronic Hepatitis C Virus with Advanced Liver Fibrosis
  49. The Significance of Articular Hand Manifestations in Chronic HCV Patients
  50. Anti-diuretic hormone and genetic study in primary nocturnal enuresis
  51. PP237-MON PREVALENCE OF RISK FACTORS FOR METABOLIC SYNDROME IN OBESE ADOLESCENTS
  52. Distinct Ocular Expression in Infants and Children With Down Syndrome in Cairo, Egypt
  53. Age–Related Differences in Body Composition in Egyptian Obese Females
  54. Assessment of metal content and oxidative stress in autistic Egyptian patients
  55. Screening seven common mitochondrial mutations in 28 Egyptian patients with suspected mitochondrial disease
  56. Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy
  57. Growth curves of Egyptian patients with Turner syndrome
  58. Clinical significance of inflammatory and fibrogenic cytokines in diabetic nephropathy
  59. A cephalometric study of skulls from the Bahriyah oasis
  60. P53 protein and Ki-67 expression in chronic gastritis patients with positive Helicobacter pylori infection
  61. Sexual dysfunction in males with hepatitis C virus: Relevance to histopathologic changes and peginterferon treatment
  62. Variable Associations of Klinefelter Syndrome in Children
  63. Predictive Value Of Biochemical Markers In Pregnancy Induced Hypertension
  64. Management of rare side effects of peginterferon and ribavirin therapy during hepatitis C treatment: a case report
  65. Polyploidy in chronic lymphocytic leukemia with p53 deletion detected by fish: a case report
  66. The Effect of Diet on Antioxidant Status in Patients with Galactosemia