(Q60167717)

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Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816952%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816952%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

permanent neonatal diabetes mellitus

1 reference

based on heuristic

inferred from title

insulin therapy

1 reference

based on heuristic

inferred from title

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816952%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

10

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26 December 2019

Fabrizio Barbetti

15

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26 December 2019

Francesco Cerutti

5

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F Cerutti

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Europe PubMed Central

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26 December 2019

author name string

G Tonini

1

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26 December 2019

R Bonfanti

3

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Europe PubMed Central

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26 December 2019

M Vanelli

4

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Europe PubMed Central

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26 December 2019

E Faleschini

6

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26 December 2019

F Meschi

7

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26 December 2019

F Prisco

8

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26 December 2019

E Ciacco

9

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26 December 2019

C Torelli

11

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26 December 2019

V Cauvin

12

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26 December 2019

S Tumini

13

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26 December 2019

D Iafusco

14

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26 December 2019

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

16

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Europe PubMed Central

PubMed publication ID

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26 December 2019

publication date

1 July 2006

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Europe PubMed Central

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26 December 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816952%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

49

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Europe PubMed Central

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26 December 2019

9

1 reference

Europe PubMed Central

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26 December 2019

2210-2213

1 reference

Europe PubMed Central

PubMed publication ID

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26 December 2019

https://scigraph.springernature.com/pub.10.1007/s00125-006-0329-x

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relapsing diabetes can result from moderately activating mutations in KCNJ11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATP and sulfonylurea sensitivity of mutant ATP-sensitive K+ channels in neonatal diabetes: implications for pharmacogenomic therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16816952

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00125-006-0329-X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816952%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16816952%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

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