Search

Your search keyword '"Al-Saffar M"' showing total 76 results

Search Constraints

Start Over You searched for: Author "Al-Saffar M" Remove constraint Author: "Al-Saffar M"
76 results on '"Al-Saffar M"'

Search Results

1. Global multi-stakeholder endorsement of the MAFLD definition

2. The Association of Helmet Use with the Occurrence of Maxillofacial Injuries Following Bicycle or Scooter Accidents:A Retrospective Cohort Study

6. Chloroquine and hydroxychloroquine effectiveness in human subjects during coronavirus: a systematic review

14. Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

15. Toward an integrated sustainable urban design framework in the historic center of Baghdad

16. Ovarian germ-cell tumor occurring in a BRCA2 mutation carrier

17. High risk and impact factors on construction management process − case study of COVID-19 of a hospital in Iraq

18. Association between HLA-DR antigens and rheumatoid arthritis in Arabs

20. New Efficient Bridgeless Cuk Rectifiers for PFC Applications.

24. HLA-DR and tuberculin tests in rheumatoid arthritis and tuberculosis.

25. Antibody levels to mycobacteria in relation to HLA type: evidence for non-HLA-linked high levels of antibody to the 65 kD heat shock protein of M. bovis in rheumatoid arthritis

26. Global multi-stakeholder endorsement of the MAFLD definition

27. Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions.

28. Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.

29. EVALUATION OF PAIN-KILLING ACTION OF ACETYLSALICYLIC ACID NANOPARTICLES ON THERMAL NOCICEPTION IN MICE.

30. THE IMPACT OF ALOE VERA GEL ON REMINERALIZATION OF THE TOOTH AND ITS EFFECT AGAINST ENTEROCOCCUS FAECALIS: AN IN VITRO STUDY.

31. Long non-coding RNAs: The modulators of innate and adaptive immune cells.

32. Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.

33. Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability.

34. The Effect of 24/7, Digital-First, NHS Primary Care on Acute Hospital Spending: Retrospective Observational Analysis.

35. A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features.

36. Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome.

37. PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features.

38. Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

39. Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophy.

40. Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior.

41. Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features.

42. Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.

43. Katanin p80 regulates human cortical development by limiting centriole and cilia number.

44. METTL23, a transcriptional partner of GABPA, is essential for human cognition.

45. Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans.

46. Using whole-exome sequencing to identify inherited causes of autism.

47. Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene.

48. A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts.

49. Developmental and degenerative features in a complicated spastic paraplegia.

50. Phenotype of a patient with pure partial trisomy 2p(p23-->pter).

Catalog

Books, media, physical & digital resources