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2. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

4. British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders

5. Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study

6. GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

7. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

8. A Multicentre UK-Based Audit on Acquired C1 Inhibitor Deficiency 2021

9. Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK

10. Outcomes Following SARS-CoV-2 Infection in Patients With Primary and Secondary Immunodeficiency in The United Kingdom

11. Whole-genome sequencing of patients with rare diseases in a national health system

14. COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience

15. Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

16. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

17. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

18. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

19. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

21. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018)

22. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

24. Erratum to: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (Scientific Reports, (2018), 8, 1, (1300), 10.1038/s41598-017-14403-y)

26. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

28. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

29. De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

30. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

31. Additional file 2: of Primary immunodeficiency associated with chromosomal aberration – an ESID survey

32. Additional file 3: of Primary immunodeficiency associated with chromosomal aberration – an ESID survey

33. Additional file 1: of Primary immunodeficiency associated with chromosomal aberration – an ESID survey

34. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

35. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

36. Primary immunodeficiency associated with chromosomal aberration – an ESID survey

37. Encephalomyelitis with Retinopathy in Common Variable Immunodeficiency (CVID).

39. Phenotypic Characterization of EIF2AK4Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

42. Knowledge about using auto-injectable adrenaline: review of patients' case notes and interviews with general practitioners

43. Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study

44. DEDICATION.

46. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

47. Knowledge about using auto-injectable adrenaline: review of patients' case notes and interviews with general practitioners.

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