33 results on '"Bhatnagar, Pallav"'
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2. Comparison between Non-VAP and VAP patients with acquired brain injury those were admitted in intensive care unit
3. Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials
4. Efficacy of MCIMT with Auditory Cueing in order to Augment Functional Motor Recovery of Chronic Hemiparetic Arm.
5. Stress-Dependent Association Between Polygenic Risk for Schizophrenia and Schizotypal Traits in Young Army Recruits
6. Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood
7. Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia
8. Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia
9. Intravenous thrombolysis in acute ischaemic stroke: a systematic review and meta-analysis to aid decision making in patients over 80 years of age
10. Ultrasound scan in the emergency department revealed rare but potentially dangerous internal jugular vein thrombosis
11. Association studies of catechol-O-methyltransferase (COMT) gene with schizophrenia and response to antipsychotic treatment
12. Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms
13. Genetically Predicted Glucose-Dependent Insulinotropic Polypeptide (GIP) Levels and Cardiovascular Disease Risk Are Driven by Distinct Causal Variants in the Region.
14. Pharmacogenomics of β2-agonist: key focus on signaling pathways
15. Variable therapeutic response in asthma: a genetic perspective
16. β2-adrenergic receptor polymorphisms and asthma in the North Indian population
17. β2-adrenergic receptor polymorphisms and response to salbutamol among Indian asthmatics∗
18. Prevalence and cardiometabolic correlates of ketohexokinase gene variants among UK Biobank participants.
19. A Pilot Genome‐Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH.
20. Salmonella spinal osteomyelitis: A case report and review of literature
21. <italic>ADCY9</italic> Genetic Variants and Cardiovascular Outcomes With Evacetrapib in Patients With High-Risk Vascular Disease: A Nested Case-Control Study.
22. Coding variants in PNPLA3 and TM6SF2 are risk factors for hepatic steatosis and elevated serum alanine aminotransferases caused by a glucagon receptor antagonist.
23. Genetic Variants in Platelet Factor 4 Modulate Inflammatory and Platelet Activation Biomarkers.
24. A Genome-Wide Association Study of Total Bilirubin and Cholelithiasis Risk in Sickle Cell Anemia.
25. Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
26. HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.
27. Pharmacogenomics of β2-agonist: key focus on signaling pathways.
28. Youth's mental health in Jeopardy: A call for attention
29. Profound opiate toxicity in gastroparesis following therapeutic dose.
30. Genome-Wide Meta-Analysis of Systolic Blood Pressure in Children with Sickle Cell Disease.
31. Association of DRD2 gene variant with schizophrenia
32. rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis.
33. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.
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