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1,174 results on '"Jayakar A"'

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1. De novo variants in GABRA4 are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy

3. Intraductal Papilloma of the Breast: A Case Report

4. Management of Pustular Psoriasis; The Way Ahead

5. Small Molecules in the Management of Psoriasis and Psoriatic Arthritis

6. Effect of COVID-19 lockdowns on maxillofacial fractures in New Zealand: a retrospective study

8. Enhancing High-Speed Data Communications: Optimization of Route Controlling Network on Chip Implementation

10. Monitoring and integrated care coordination of patients with alpha-mannosidosis: A global Delphi consensus study

11. The impact of clinical genome sequencing in a global population with suspected rare genetic disease

12. Role of Phenol Epidural Neurolysis in Pain Management of Patient with Myxofibrosarcoma: A Case Report

13. A Study Comparing the Aerosol Box and Mayo Containment setup During Intubation in COVID-negative Indian Patients as a Learning Curve

14. Delayed orbital floor implant complications: Case report and review of the literature

15. Incisional Hernia with Rare Finding of Liver as Content: A Case Report

16. Open Surgical Retrieval of a Foreign Body in the Neck: A Case Report

18. Human OPRM1 and murine Oprm1 promoter driven viral constructs for genetic access to μ-opioidergic cell types

19. Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting

21. P486: A global Delphi consensus approach to monitoring and integrated care coordination of patients with alpha-mannosidosis

22. Human OPRM1 and murine Oprm1 promoter driven viral constructs for genetic access to μ-opioidergic cell types

23. Acne mimickers: Differential diagnosis of open comedones – A short review

26. Type IVA Choledochal Cyst in Adult: A Case Report

27. Scalable generation of sensory neurons from human pluripotent stem cells

28. SARS-CoV-2 replication in airway epithelia requires motile cilia and microvillar reprogramming

30. Report of two cases of Schaaf‐Yang syndrome: Same genotype and different phenotype

33. Conformation-locking antibodies for the discovery and characterization of KRAS inhibitors

35. Prospective intraoperative and histologic evaluation of cavernous sinus medial wall invasion by pituitary adenomas and its implications for acromegaly remission outcomes

38. Impact of sociodemographic status and sex on chronic rhinosinusitis and olfaction in people with cystic fibrosis.

42. ITSN1: a novel candidate gene involved in autosomal dominant neurodevelopmental disorder spectrum

45. Determinants of SARS-CoV-2 entry and replication in airway mucosal tissue and susceptibility in smokers

46. Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3

47. UBA2 variants underlie a recognizable syndrome with variable aplasia cutis congenita and ectrodactyly

48. An unusual cause of multiple penile ulcers and balanoposthitis in a young male

49. Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

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