(Q46736681)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Transient neonatal diabetes mellitus is associated with a recurrent (R201H) KCNJ11 (KIR6.2) mutation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

transient neonatal diabetes mellitus

7 January 2020

main subject

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Maria F. Faienza

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Luciano Cavallo

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Fabrizio Barbetti

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

C Colombo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

C Zecchino

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Early Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

5 October 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

48

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

11

1 reference

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7 January 2020

page(s)

2439-2441

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16205880%20AND%20SRC:MED&resulttype=core&format=json

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

7 January 2020

cites work

1 reference

12 December 2020

Neonatal and very-early-onset diabetes mellitus

1 reference

12 December 2020

Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2.

1 reference

12 December 2020

Glucose-sensing in glucagon-like peptide-1-secreting cells

1 reference

12 December 2020

The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R2

1 reference

12 December 2020

KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

1 reference

12 December 2020

Relapsing diabetes can result from moderately activating mutations in KCNJ11.

1 reference

12 December 2020

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

1 reference

12 December 2020

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients

1 reference

12 December 2020