Add to ORKGThe finding that patients with diabetes due to potassium channel mutations can transfer from insulin to sulfonylureas has revolutionised the management of patients with permanent neonatal diabetes. The extent to which the in vitro characteristics of the mutation can predict a successful transfer is not known. Our aim was to identify factors associated with successful transfer from insulin to sulfonylureas in patients with permanent neonatal diabetes due to mutations in KCNJ11 (which encodes the inwardly rectifying potassium channel Kir6.2)
Article type: case reportThis is the author accepted manuscript.Final version available from Wiley v...
Background: KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive pota...
Activating missense mutations in the gene encoding potassium inwardly rectifying channel, subfamily...
The finding that patients with diabetes due to potassium channel mutations can transfer from insulin...
This is the final version of the article. Available from Springer Verlag via the DOI in this record....
Background Permanent neonatal diabetes caused by mutations in the KCNJ11 gene may be managed with hi...
A ctivating mutations in the KCJN11gene encoding in the ATP-sensitiveK channel (KATP channel) subun...
Permanent neonatal diabetes mellitus is most commonly caused by mutations in the ATP-sensitive potas...
Permanent neonatal diabetes mellitus refers to diabetes that occurs before the age of 6 months and p...
Permanent neonatal diabetes (PNDM) can result from activating heterozygous mutations in KCNJ11 gene,...
OBJECTIVE - Neonatal diabetes can result from mutations in the Kir6.2 or sulfonylurea receptor 1 (SU...
KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive potassium channe...
Background KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive potas...
Permanent neonatal diabetes (PND) can be caused by mutations in the transcription factors insulin pr...
Article type: case reportThis is the author accepted manuscript.Final version available from Wiley v...
Background: KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive pota...
Activating missense mutations in the gene encoding potassium inwardly rectifying channel, subfamily...
The finding that patients with diabetes due to potassium channel mutations can transfer from insulin...
This is the final version of the article. Available from Springer Verlag via the DOI in this record....
Background Permanent neonatal diabetes caused by mutations in the KCNJ11 gene may be managed with hi...
A ctivating mutations in the KCJN11gene encoding in the ATP-sensitiveK channel (KATP channel) subun...
Permanent neonatal diabetes mellitus is most commonly caused by mutations in the ATP-sensitive potas...
Permanent neonatal diabetes mellitus refers to diabetes that occurs before the age of 6 months and p...
Permanent neonatal diabetes (PNDM) can result from activating heterozygous mutations in KCNJ11 gene,...
OBJECTIVE - Neonatal diabetes can result from mutations in the Kir6.2 or sulfonylurea receptor 1 (SU...
KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive potassium channe...
Background KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive potas...
Permanent neonatal diabetes (PND) can be caused by mutations in the transcription factors insulin pr...
Article type: case reportThis is the author accepted manuscript.Final version available from Wiley v...
Background: KCNJ11 mutations cause permanent neonatal diabetes through pancreatic ATP-sensitive pota...
Activating missense mutations in the gene encoding potassium inwardly rectifying channel, subfamily...