333 results on '"Koçak N"'
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2. Evaluation of the Relationship Between Suicide Behavior and SIRT-1 Gene in Patients with Schizophrenia and Other Psychotic Disorders
3. Evaluation of the relationship between suicidal behavior and the sirt1 gene in patients with schizophrenia
4. Conventional Internal Limiting Membrane Peeling Versus Temporal Inverted Internal Limiting Membrane Flap Technique for Large Macular Holes: A Comparative Study
5. Synthesis of iminooxime derivatives and investigation of their complexes
6. Prospective cross-sectional multicenter study on domiciliary noninvasive ventilation in stable hypercapnic COPD patients
7. Mutation analysis in Turkish patients with hereditary fructose intolerance
8. Short-term effect of captopril on microalbuminuria in children with glycogen storage disease type Ia
9. MERMAID SYNDROME - A CASE REPORT: A70
10. COMMUNICATION NETWORKS AND COOPERATION REGIMES OF INTERNATIONAL DISTANCE EDUCATION ORGANIZATIONS
11. Determination of antibiotic susceptibility, ESBL genes and pulsed-field gel electrophoresis profiles of extended-spectrum ?-lactamase-containing escherichia coli isolates [Genişlemiş spektrumlu ?-laktamaz üreten Escherichia coli izolatlarının antibiyotik duyarlılıklarının, GSBL genlerinin ve pulsed-field jel elektroforez yöntemiyle genotipik profillerinin belirlenmesi]
12. Type I hereditary tyrosinaemia: Presentation of 11 cases
13. Helicobacter pylori Infection in Children with Cirrhosis
14. Glucose-6-phosphatase gene mutations in Turkish patients with glycogen storage disease type Ia
15. Long term follow up of interferon responder children with chronic hepatitis B
16. HIGHER-DOSE INTERFERON ALFA RETREATMENT IN CHILDREN WITH CHRONIC HEPATITIS B
17. Santral seröz koryoretinopatide yarim doz tek uygulamalik fotodinamik tedavinin sonuçlari
18. Successful treatment of polyarteritis nodosa with interferon alpha in a nine-month old girl
19. Analysis of three mutations in Turkish children with Gaucher disease
20. Eriskin tip foveomaküler vitelliform distrofili bir olgu sunumu
21. Prematüre retinopatisinde risk faktörleri ve tarama sonuçlar
22. A patient with choroidal metastases from invasive urothelial bladder cancer
23. A case with multipe evanescent white dot syndrome
24. Yüksek Doz İnterferon-Alfa 2b İle Tedavi Edilen Delta Hepatiti Tanılı Hastada Retinopati Gelişmesi: Olgu Sunumu
25. Akut Gastroenteritli Olguların Başvuru Sırasındaki Bulgularının Ve Tedaviye Yanıtlarının Değerlendirilmesi
26. Retinoblastomun Tedavi Kararındaki Zorluklar
27. The place and the efficacy of infectious disease consultations in the hospitals
28. Prevalence of hepatitis A antibodies in children with chronic liver disease and other gastrointestinal diseases
29. Sistemik skleroz hastalarında göz tutulumunun değerlendirilmesi
30. Evaluation of confounding factors interfering with sexual function in women with minimal pelvic organ prolapse
31. Global Tendencies in Open and Distance Learning
32. Anne adaylarına verilen eğitimin gebelik, doğum ve lohusalığa ilişkin geleneksel uygulamalara etkisi
33. Integrating Social Media Into Distance Learning
34. Titanium dioxide nanoparticles induce cytotoxicity and reduce mitotic index in human amniotic fluid-derived cells
35. Does the imbalance between agonistic and antagonistic IL-1 play a role in progression of febrile convulsions?
36. Filtering short term fluctuations in inflation analysis
37. DNA haplotype analysis for the diagnosis of Wilson disease in siblings
38. Titanium dioxide nanoparticles induce cytotoxicity and reduce mitotic index in human amniotic fluid-derived cells.
39. Valproate-induced Insulin Resistance in Prepubertal Girls with Epilepsy
40. Helicobacter pylori diagnosis in children with liver cirrhosis
41. Management of Free Floating Iris Cysts in the Anterior Chamber: A Case Report
42. Cutaneous Anthrax in Turkey: A Review of 32 Cases
43. The effect of ursodeoxycholic acid in children with prolonged hepatitis A virus infection that may be a trigger factor for autoimmune hepatitis
44. Lamivudine for children with chronic hepatitis B
45. Obesity: a cause of steatohepatitis in children
46. DNA haplotype analysis for the diagnosis of Wilson disease in siblings
47. The prevalence of Familial Mediterranean Fever common gene mutations in patients with simple febrile seizures.
48. Type I hereditary tyrosinaemia: Presentation of 11 cases
49. Nonfunctioning Allografts Play an Important Role in Parathyroid Hormone and Calcitonin Metabolism
50. Chloroquine Phosphate Reduces the Frequency of Muscle Cramps during Maintenance Hemodialysis
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