Search

Your search keyword '"Allcock R"' showing total 223 results

Search Constraints

Start Over You searched for: Author "Allcock R" Remove constraint Author: "Allcock R"
223 results on '"Allcock R"'

Search Results

1. Immunomodulatory therapy in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS, MIS-C; RECOVERY): a randomised, controlled, open-label, platform trial

2. Empagliflozin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial

11. HIGHLIGHTS ACROSS MYOLOGY

14. Ion torrent high throughput mitochondrial genome sequencing (HTMGS)

15. Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes

22. Ion torrent high throughput mitochondrial genome sequencing (HTMGS)

26. MicroRNA signatures in malignant pleural mesothelioma effusions

27. A haplotype spanning P2X7R, P2X4R and CAMKK2 may mark susceptibility to pulmonary non-tuberculous mycobacterial disease

28. Susceptibility to non-tuberculous mycobacterial disease is influenced by rs1518111 in IL10

29. Erdheim-Chester disease associated with a novel, complex BRAF p.Thr599_Val600delinsArgGlu mutation

30. Microbial Functional Capacity Is Preserved Within Engineered Soil Formulations Used In Mine Site Restoration

32. Genetic Characterization of Archived Bunyaviruses and their Potential for Emergence in Australia

34. Polymorphisms in CAMKK2 may predict sensory neuropathy in African HIV patients

38. A germline MTOR mutation in Aboriginal Australian siblings with intellectual disability, dysmorphism, macrocephaly, and small thoraces

39. A germline MTOR mutation in Aboriginal Australian siblings with intellectual disability, dysmorphism, macrocephaly, and small thoraces

40. Combined DNA, toxicological and heavy metal analyses provides an auditing toolkit to improve pharmacovigilance of traditional Chinese medicine (TCM)

41. Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma

42. Endeavour Training

44. Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita

45. Thorough assessment of DNA preservation from fossil bone and sediments excavated from a late Pleistocenee-Holocene cave deposit on Kangaroo Island, South Australia

48. G.P.18

Catalog

Books, media, physical & digital resources