98 results on '"Bhuiyan Z"'
Search Results
2. Extreme variability in clinical penetrance for a splice-site Plakophilin-2 mutation in a Bangladeshi family
3. Genotype–phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia
4. Calmodulin mutations and life-threatening cardiac arrhythmias: Insights from the International Calmodulinopathy Registry
5. 511 Organising A Surgical Conference During The COVID-19 Pandemic – Is It ‘Virtually’ The Same?
6. Arrhythmogenic right ventricular cardiomyopathy: asymptomatic to life threatening as illustrated by the cases of two sisters
7. An Unusual Presentation of Malignant Melanoma
8. Simultaneous analysis of the behavioural phenotype, physical factors, and parenting stress in people with Cornelia de Lange syndrome
9. Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience
10. Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties
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
14. Knowledge, Attitude and Perception (KAP) about Renal Transplantation of CKD Patients and their Care Givers
15. Evolution of mechanics in α-helical peptide conjugated linear- and star-block PEG
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
18. Congenital primary arrhythmias in children
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
22. Studies of the Physico-Mechanical, Interfacial, and Degradation Properties of Jute Fabrics/Melamine Composites
23. MP-01.02 Nephrostomy Tubeless and JJ Stentless PCNL: Experience of 113 Cases
24. UP-02.048 Laparoscopic Management of Pelviureteric Junction Obstruction
25. Sudden Cardiac Death I
26. Fabrication and Mechanical Characterization of Jute Fiber-Reinforced Melamine Matrix Composite
27. Abstracts: Genetics in arrhythmias
28. Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4–S5 linker in slow inactivation
29. MP-15.17
30. MP-15.13
31. UP-01.44
32. Role of sequence variations in the human ether-a-go-go-related gene (HERG, KCNH2) in the Brugada syndrome
33. Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience
34. Substitution of a conserved alanine in the domain IIIS4–S5 linker of the cardiac sodium channel causes long QT syndrome
35. A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families
36. Outcome of 500 cases of transurethral resection of Prostate (TURP) in District level teaching Hospital.
37. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study.
38. Effect of co-monomers on the improvement of crust leather surfaces cured under UV radiation.
39. UP-01.44: Snodgrass technique of urethroplasty modified with the adjunct of techniques of substitution urethroplasty: experience in 125 cases in prospective study
40. MP-15.17: Comparison of efficacy of post-TURBT adjuvant intravesical mitomycin C therapy in preventing the recurrence of intermediate risk superficial TCC: peri-operative single dose versus delayed multi-dose regimen, short- versus long-term result
41. MP-15.13: Post TURBT intensive and long-term maintenance intravesical mitomycin C for managing superficial TCC in Bangladeshi patients: interim results of an ongoing prospective study
42. Further analysis of N*.rho. and N*.omega. quasi-two-body reactions by 5 GeV/c \pi^{+} mesons on protons
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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