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1. Identification of a New IgG mAb Format with Enhanced Complement Mediated Effector Function and Extended Half Life

4. Calmodulin mutations and life-threatening cardiac arrhythmias: Insights from the International Calmodulinopathy Registry

11. Genetic Mosaicism in Calmodulinopathy

12. COLREGS-COMPLIANT PATH PLANNING FOR AUTONOMOUS SURFACE VEHICLES: A MULTIOBJECTIVE OPTIMIZATION APPROACH

13. Betulinic acid and its ionic derivatives impaired growth of prostate cancer cells without induction of GRP78 and CHOP

16. Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes

17. Familial primary arrhythmias: Genes, mechanisms and treatment: Present perspective

19. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study

20. Evaluation of Broiler Health Status Through Flock Health Monitoring Program in Bangladesh

21. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia

25. Sudden Cardiac Death I

27. Abstracts: Genetics in arrhythmias

29. MP-15.17

30. MP-15.13

31. UP-01.44

36. Outcome of 500 cases of transurethral resection of Prostate (TURP) in District level teaching Hospital.

38. Effect of co-monomers on the improvement of crust leather surfaces cured under UV radiation.

43. A Malay boy with the Cornelia de Lange syndrome: Clinical and molecular findings

44. Molecular diagnostics of catecholaminergic polymorphic ventricular tachycardia using denaturing high-performance liquid chromatography and sequencing

45. Letters regarding article by Coronel et al, 'Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: A combined electrophysiological, genetic, histopathologic, and computational study' - Response

46. Selective acquired long QT syndrome (saLQTS) upon risperidone treatment

47. Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties.

48. Distinguishing arrhythmogenic right ventricular cardiomyopathy/dysplasia-associated mutations from background genetic noise.

49. Genetic Mosaicism in Calmodulinopathy

50. Novel Calmodulin Mutations Associated with Congenital Long QT Syndrome Affect Calcium Current in Human Cardiomyocytes

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