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377 results on '"Sanjay M"'

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1. The risk of knee pain and knee osteoarthritis in professional footballers

2. Beyond the global brain differences : intraindividual variability differences in 1q21.1 distal and 15q11.2 bp1-bp2 deletion carriers

3. Beyond the Global Brain Differences:Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers

4. Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation

5. Machine Learning Based User Transaction Alert Using Decentralized Approach-SOS

6. Confidence and Assurance of Percentiles

7. Spectrum of epilepsy with eyelid myoclonia: Delineation of disease subtypes from a large multicenter study

8. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

9. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

10. Reprint of: Prevalence and Characteristics of Root Resorption Identified in Cone-Beam Computed Tomography Scans.

11. Correlation Coefficients and Adaptive Threshold-Based Dissolve Detection in High-Quality Videos

12. Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin.

13. Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome

14. MR appearance of a rare ameloblastic fibroma with formation of dental hard tissues with histopathologic correlation:a case report

15. Computation of Reliability Statistics for Finite Samples of Success-Failure Experiments

16. Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome

17. SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility

18. Local molecular and global connectomic contributions to cross-disorder cortical abnormalities.

19. Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.

20. A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.

21. MR appearance of a rare ameloblastic fibroma with formation of dental hard tissues with histopathologic correlation: a case report

22. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.

23. Prognostic factors for lymph node metastasis from upper gingival carcinomas.

24. Radiation-induced undifferentiated spindle cell sarcoma following high-dose-rate interstitial brachytherapy for tongue squamous cell carcinoma.

25. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

26. Prognostic factors for lymph node metastasis from upper gingival carcinomas:[Inkl. correction]

27. Effect of Timing Error: A Case Study of Navigation Camera

28. Genomic and transcriptomic correlates of immunotherapy response within the tumor microenvironment of leptomeningeal metastases

29. The ENIGMA-Epilepsy working group: Mapping disease from large data sets.

30. Marek's disease virus Meq oncoprotein interacts with chicken HDAC 1 and 2 and mediates their degradation via proteasome dependent pathway.

31. Structural brain imaging studies offer clues about the effects of the shared genetic etiology among neuropsychiatric disorders.

32. Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

33. PWM CONTROLLED FOUR SWITCH THREE PHASE INVERTER FED INDUCTION MOTOR DRIVE

34. Structural brain imaging studies offer clues about the effects of the shared genetic etiology among neuropsychiatric disorders

35. RHOBTB2 Mutations Expand the Phenotypic Spectrum of Alternating Hemiplegia of Childhood

36. Climate change and epilepsy: Insights from clinical and basic science studies.

37. Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications

38. Climate change and epilepsy: Insights from clinical and basic science studies

39. Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy

40. Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

41. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

42. Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study.

43. DOORS syndrome and a recurrent truncating ATP6V1B2 variant

44. Oxidative torrefaction for cleaner utilization of biomass for soil amendment

45. Real-life survey of pitfalls and successes of precision medicine in genetic epilepsies

46. Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity

47. Diffusion-weighted magnetic resonance imaging of the oral and maxillofacial region:optimal fat suppression method

48. 1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

49. Mechanisms of lymphoma clearance induced by high-dose alkylating agents

50. Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

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