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60 results on '"Wesam Kurdi"'

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1. Sexually transmitted infections in the middle east and North Africa: comprehensive systematic review and meta-analysis

2. Management of twin reversed arterial perfusion sequence: one center's experience

3. Observational cohort study of perinatal outcomes of women with COVID-19

4. Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

5. Assessment of Quality of the Electronic Education System in the Corona Crisis Period: Applied Study on Al al-Bayt University

8. Chorioangioma: a single tertiary care center retrospective study

9. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes

10. Knowledge and attitudes regarding non‐invasive prenatal testing among women in Saudi Arabia

11. In Utero Intervention for Isolated Fetal Pleural Effusion: A Case Report

12. Efficacy of hyoscine in pain management during hysteroscopy: a systematic review and meta-analysis

13. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes

14. Prenatal exome sequencing and chromosomal microarray analysis in fetal structural anomalies in a highly consanguineous population reveals a propensity of ciliopathy genes causing multisystem phenotypes

15. The Evolution of Fetal Procedures

16. Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families

17. The effect of hyoscine-N-butylbromide on pain perception during and after hysterosalpingography in infertile women: a systematic review and meta-analysis of randomised controlled trials

18. Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies

19. Molecular autopsy in maternal–fetal medicine

20. KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis

21. Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease

22. Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation

23. The genetic landscape of familial congenital hydrocephalus

24. Renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations in a Saudi Arabian family

25. Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

26. Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families

27. The many faces of peroxisomal disorders: Lessons from a large Arab cohort

28. Autozygome and high throughput confirmation of disease genes candidacy

29. Corrigendum: Autozygosity reveals recessive mutations and novel mechanisms in dominant genes: implications in variant interpretation

30. Correction to: Expanding the genetic heterogeneity of intellectual disability

31. Obstetric outcomes in reduced and non-reduced twin pregnancies. A single hospital experience

32. The Effect of Using an Electronic Instructional Game in Improving English Language Vocabulary for Third Graders in Irbid City

33. The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

34. The genetic landscape of familial congenital hydrocephalus

35. Expanding the genetic heterogeneity of intellectual disability

36. Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population

37. Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs

39. Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families

40. Identification of a novel MKS locus defined by TMEM107 mutation

41. Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families

42. Sensitive assay for the determination of cefazolin or ceftriaxone in plasma utilizing LC

43. Fetal heart rate and umbilico-placental Doppler flow velocity waveforms in early pregnancies with a chromosomal abnormality and/or an increased nuchal translucency thickness

44. Mutation in MPDZ causes severe congenital hydrocephalus

45. Genomic analysis of Meckel-Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes

46. Prenatal diagnosis and treatment perspective of fetal hypothyroidism with goiter

47. Robot-assisted surgical staging for ovarian cancer in pregnant women

48. Reliable prenatal diagnosis of Canavan disease by measuring N-acetylaspartate in amniotic fluid using liquid chromatography tandem mass spectrometry

49. Stable isotope dilution analysis of N-acetylaspartic acid in urine by liquid chromatography electrospray ionization tandem mass spectrometry

50. P08.08: Cerebroplacental ratio and its association with adverse perinatal outcomes in early and late onset intrauterine growth restriction (IUGR)

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