Central nervous system (CNS) features in children with permanent neonatal diabetes (PNDM) due to KCNJ11 mutations have a major impact on affected families. Sulfonylurea therapy achieves outstanding metabolic control but only partial improvement in CNS features. The effects of KCNJ11 mutations on the adult brain and their functional impact are not well understood. We aimed to characterize the CNS features in adults with KCNJ11 PNDM compared with adults with INS PNDM.This article is freely available via Open Access. The final published article is available from the Publisher URL (above
Item does not contain fulltextBACKGROUND: KCNJ11 mutations are a common cause of diabetes diagnosed ...
Objective. Mutations of the KCNJ11 gene are the most common cause of the permanent neonatal diabetes...
OBJECTIVE - Activating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channe...
Central nervous system (CNS) features in children with permanent neonatal diabetes (PNDM) due to KCN...
This is the author accepted manuscript. The final version is available from American Diabetes Associ...
OBJECTIVEdTo assess performance on an age-standardized neuromotor coordination task among sulfonylur...
KCNJ11 encodes Kir6.2, the pore-forming subunit of the ATP-sensitive potassium channel present in br...
Background KCNJ11 mutations are a common cause of diabetes diagnosed in the first 6 months of life, ...
Heterozygous activating mutations in the gene encoding for the ATP-sensitive potassium channel subun...
OBJECTIVEdActivating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channel, ...
OBJECTIVE: Activating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channel,...
Aims/hypothesis Activating mutations in the KCNJ11 gene encoding the Kir6.2 subunit of the K-ATP cha...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
Mutations in the KCNJ11 gene, which encodes the Kir6.2 subunit of the pancreatic KATP channel, cause...
Item does not contain fulltextBACKGROUND: KCNJ11 mutations are a common cause of diabetes diagnosed ...
Objective. Mutations of the KCNJ11 gene are the most common cause of the permanent neonatal diabetes...
OBJECTIVE - Activating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channe...
Central nervous system (CNS) features in children with permanent neonatal diabetes (PNDM) due to KCN...
This is the author accepted manuscript. The final version is available from American Diabetes Associ...
OBJECTIVEdTo assess performance on an age-standardized neuromotor coordination task among sulfonylur...
KCNJ11 encodes Kir6.2, the pore-forming subunit of the ATP-sensitive potassium channel present in br...
Background KCNJ11 mutations are a common cause of diabetes diagnosed in the first 6 months of life, ...
Heterozygous activating mutations in the gene encoding for the ATP-sensitive potassium channel subun...
OBJECTIVEdActivating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channel, ...
OBJECTIVE: Activating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channel,...
Aims/hypothesis Activating mutations in the KCNJ11 gene encoding the Kir6.2 subunit of the K-ATP cha...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
This is the author accepted manuscript. The final version is available from Wiley via the DOI in thi...
Mutations in the KCNJ11 gene, which encodes the Kir6.2 subunit of the pancreatic KATP channel, cause...
Item does not contain fulltextBACKGROUND: KCNJ11 mutations are a common cause of diabetes diagnosed ...
Objective. Mutations of the KCNJ11 gene are the most common cause of the permanent neonatal diabetes...
OBJECTIVE - Activating mutations in the KCNJ11 gene, encoding the Kir6.2 subunit of the KATP channe...