239 results on '"Shepherd, Maggie"'
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2. Patient preference for second- and third-line therapies in type 2 diabetes: a prespecified secondary endpoint of the TriMaster study
3. Association of birthweight and penetrance of diabetes in individuals with HNF4A-MODY: a cohort study
4. Implementing a strategic plan for research.
5. Fundamental nursing care in patients with the SARS-CoV-2 virus: results from the ‘COVID-NURSE’ mixed methods survey into nurses’ experiences of missed care and barriers to care
6. Living in the cracks: Two novel genera of Variosea (Amoebozoa) discovered on an urban sidewalk.
7. Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
8. A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metformin
9. Incretin hormone responses to carbohydrate and protein/fat are preserved in adults with sulfonylurea‐treated KCNJ11 neonatal diabetes.
10. Screening for neonatal diabetes at day 5 of life using dried blood spot glucose measurement
11. Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes
12. Nurses' strategies for overcoming barriers to fundamental nursing care in patients with COVID-19 caused by infection with the SARS-COV-2 virus: Results from the 'COVID-NURSE' survey
13. Nurses' strategies for overcoming barriers to fundamental nursing care in patients with COVID‐19 caused by infection with the SARS‐COV‐2 virus: Results from the 'COVID‐NURSE' survey.
14. Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases
15. Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation
16. Most People With Long-Duration Type 1 Diabetes in a Large Population-Based Study Are Insulin Microsecretors
17. A diagnosis of monogenic neonatal diabetes can improve treatment and glycaemic control
18. Differential diagnosis: identifying people with monogenic diabetes
19. The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype
20. Monogenic diabetes and the role of the diabetes nurse
21. Impact of misdiagnosis in HNF1A diabetes: a case study
22. Are genetic tests exceptional? Lessons from a qualitative study on thrombophilia
23. Integration of the MODY link nurse project: 20-month evaluation
24. MODY link nurses: pushing the boundaries of diabetes nursing
25. GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency
26. Meeting the needs of young people with diabetes: an ongoing challenge
27. Integrating genetics into diabetes care: a new role for DSNs
28. Improvements in Awareness and Testing Have Led to a Threefold Increase Over 10 Years in the Identification of Monogenic Diabetes in the U.K.
29. Bridging the gap between research and clinical care: strategies to increase staff awareness and engagement in clinical research.
30. Urinary C-Peptide Creatinine Ratio Is a Practical Outpatient Tool for Identifying Hepatocyte Nuclear Factor 1-α/Hepatocyte Nuclear Factor 4-α Maturity-Onset Diabetes of the Young From Long-Duration Type 1 Diabetes
31. Urinary C-peptide creatinine ratio is a practical outpatient tool for identifying hepatocyte nuclear factor 1-α/ hepatocyte nuclear factor 4-α maturity-onset diabetes of the young from long-duration type 1 diabetes
32. Impact of COVID‐19 and other infectious conditions requiring isolation on the provision of and adaptations to fundamental nursing care in hospital in terms of overall patient experience, care quality, functional ability, and treatment outcomes: systematic review
33. Insulin Mutation Screening in 1,044 Patients With Diabetes: Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood
34. The impact of thyroid eye disease upon patientsʼ wellbeing: a qualitative analysis
35. GATA6 cooperates with EOMES/SMAD2/3 to deploy the gene regulatory network governing human definitive endoderm and pancreas formation
36. Targeted diabetes education for care home teams
37. Insulin initiation in primary care: helping it happen
38. Neonatal diabetes is more than just a paediatric problem: 57 years of diabetes from a Kir6.2 mutation
39. β-Cell Dysfunction, Insulin Sensitivity, and Glycosuria Precede Diabetes in Hepatocyte Nuclear Factor-1α Mutation Carriers
40. Studentsʼ and assessorsʼ attitudes towards studentsʼ self-assessment of their personal and professional behaviours
41. The acceptability of 360-degree judgements as a method of assessing undergraduate medical studentsʼ personal and professional behaviours
42. ‘I donʼt feel like a diabetic any more’: the impact of stopping insulin in patients with maturity onset diabetes of the young following genetic testing
43. No Deterioration in Glycemic Control in HNF-1α Maturity-Onset Diabetes of the Young Following Transfer From Long-Term Insulin to Sulphonylureas
44. Importance of genetic testing and recognition of neonatal diabetes: a case report
45. Intrauterine Hyperglycemia Is Associated With an Earlier Diagnosis of Diabetes in HNF-1α Gene Mutation Carriers
46. Maturity-Onset Diabetes of the Young Caused by a Balanced Translocation Where the 20q12 Break Point Results in Disruption Upstream of the Coding Region of Hepatocyte Nuclear Factor-4α (HNF4A) Gene
47. Maturity-onset diabetes of the young Caused by a balanced translocation Where the 20q12 break point results in disruption upstream of the coding region of Hepatocyte Nuclear Factor (HNF4A) gene. (Brief Genetics Report)
48. Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1β1
49. Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia
50. Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes
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