Search

Your search keyword '"Eker D"' showing total 102 results

Search Constraints

Start Over You searched for: Author "Eker D" Remove constraint Author: "Eker D"
102 results on '"Eker D"'

Search Results

1. Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants

12. Study of Heart and Renal Protection (SHARP): Randomized trial to assess the effects of lowering low-density lipoprotein cholesterol among 9,438 patients with chronic kidney disease.

13. Colonic replacement of esophagus in children

16. FACTORIAL STRUCTURE, VALIDITY, AND RELIABILITY OF THE MULTIDIMENSIONAL SCALE OF PERCEIVED SOCIAL SUPPORT

17. Genetic analyses of the NF1gene in Turkish neurofibromatosis type I patients and definition of three novel variants

21. The relative contribution of NSAIDs and H elicobacter pylori to the aetiology of endoscopically-diagnosed peptic ulcer disease: observations from a tertiary referral hospital in the UK between 2005 and 2010.

22. Attitudes toward mental illness: recognition, desired social distance, expected burden and negative influence on mental health among Turkish freshmen.

23. Micro-costing diabetic eye screening: estimation of personal expense, attendance and health care resource use

24. Micro-costing diabetic eye screening: estimation of personal expense, attendance and health care resource use

25. Micro-costing diabetic eye screening: estimation of personal expense, attendance and health care resource use

26. Micro-costing diabetic eye screening: estimation of personal expense, attendance and health care resource use

27. Micro-costing diabetic eye screening: estimation of personal expense, attendance and health care resource use

28. Micro-costing diabetic eye screening: estimation of personal expense, attendance and health care resource use

29. The Phenotypic Spectrum of Desanto-Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey.

30. Recognising symptoms of congenital myasthenic syndromes in children: A guide for paediatricians.

31. The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method.

32. A Genetics Study in the Foreskin of Boys with Hypospadias.

33. Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia.

34. Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

35. Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype.

36. Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method.

37. Customised targeted massively parallel sequencing enables more precise diagnosis of patients with epilepsy.

38. The Effect of Sugammadex on Time of Sciatic Block by Perineural Bupivacaine in Rats.

39. Comprehensive Genetic Analysis of RASopathy in the Era of Next-Generation Sequencing and Definition of a Novel Likely Pathogenic > KRAS Variation.

40. Clinical Features of Aberrations Chromosome 22q: A Pilot Study.

41. Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants.

42. Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes.

43. The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region

44. Targeted massively parallel sequencing in the management of cytogenetically normal lymphoid malignancies.

45. A Pilot Study of Identification Genetic Background of Craniosynostosis Cases.

46. Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma.

47. Relationship between arginase genes polymorphisms and preschool wheezing phenotypes.

48. Targeted High-Throughput Sequencing Analysis Results of Osteogenesis Imperfecta Patients from Different Regions of Turkey.

49. The Importance of Multiple Gene Analysis for Diagnosis and Differential Diagnosis in Charcot Marie Tooth Disease.

50. The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies.

Catalog

Books, media, physical & digital resources