24 results on '"Hattersley, Andrew T."'
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2. Identification of GCK-MODY in cases of neonatal hyperglycemia: a case series and review of clinical features
3. Identification of GCK‐ maturity‐onset diabetes of the young in cases of neonatal hyperglycemia: A case series and review of clinical features
4. The diagnosis and management of monogenic diabetes in children and adolescents
5. Permanent neonatal diabetes in siblings with novel C109Y INS mutation transmitted by an unaffected parent with somatic mosaicism
6. Home urine C-peptide creatinine ratio (UCPCR) testing can identify type 2 and MODY in pediatric diabetes
7. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia
8. Early-onset, severe lipoatrophy in a patient with permanent neonatal diabetes mellitus secondary to a recessive mutation in the INS gene
9. KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life
10. Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia
11. Persistently autoantibody negative (PAN) type 1 diabetes mellitus in children
12. Incidence of neonatal diabetes in Austria–calculation based on the Austrian Diabetes Register
13. ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents
14. Characteristics of maturity onset diabetes of the young in a large diabetes center
15. Permanent neonatal diabetes in siblings with novel C109YINSmutation transmitted by an unaffected parent with somatic mosaicism
16. Characteristics of maturity onset diabetes of the young in a large diabetes center.
17. Home urine C-peptide creatinine ratio testing can identify type 2 and MODY in pediatric diabetes
18. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia
19. KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life
20. Early-onset, severe lipoatrophy in a patient with permanent neonatal diabetes mellitus secondary to a recessive mutation in the INS gene
21. Persistently autoantibody negative (PAN) type 1 diabetes mellitus in children
22. Genetics and type 2 diabetes in youth
23. KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life.
24. ISPAD Clinical Practice Consensus Guidelines 2014. The diagnosis and management of monogenic diabetes in children and adolescents.
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