(Q38027010)

English

Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome

scientific article published on 18 July 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

Richard Palmqvist

3

object named as

Richard Palmqvist

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

author name string

Annika Winbo

1

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

Olof Sandström

2

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

Annika Rydberg

4

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

publication date

18 July 2012

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

Cardiology in the Young

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

23

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

325-334

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

GENETICAL ASPECTS OF THE CARDIO-AUDITORY SYNDROME OF JERVELL AND LANGE-NIELSEN (CONGENITAL DEAFNESS AND ELECTROCARDIOGRAPHIC ABNORMALITIES).

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

KCNQ1-dependent transport in renal and gastrointestinal epithelia

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Inner ear abnormalities in a Kcnq1 (Kvlqt1) knockout mouse: a model of Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Molecular basis of the long-QT syndrome associated with deafness

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Effect of gastrin on gastric mucosal cell proliferation in man

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Clinical course and risk stratification of patients affected with the Jervell and Lange-Nielsen syndrome.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Gastrin and cancer: a review.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Effect of Hydrochloric Acid on Iron Absorption

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: a marker of severe KCNQ1 dysfunction?

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

The cardiac K+ channel KCNQ1 is essential for gastric acid secretion

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Heartburn: cardiac potassium channels involved in parietal cell acid secretion

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

KCNQ1 is the luminal K+ recycling channel during stimulation of gastric acid secretion

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

The KCNQ1 potassium channel: from gene to physiological function

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

The endogenous Toll-like receptor 4 agonist S100A8/S100A9 (calprotectin) as innate amplifier of infection, autoimmunity, and cancer

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Heightened susceptibility to chronic gastritis, hyperplasia and metaplasia in Kcnq1 mutant mice.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Surdocardiac syndrome of Jervell and Lange-Nielsen, with prolonged QT interval present at birth, and severe anaemia and syncopal attacks in childhood

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

The surdo-cardiac syndrome: three new cases of congenital deafness with syncopal attacks and Q-T prolongation in the electrocardiogram

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

21 January 2018

Jervell and Lange-Nielsen syndrome: A Norwegian perspective

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

7 January 2021

based on heuristic

inferred from DOI database lookup

Synergistic interaction between hypergastrinemia and Helicobacter infection in a mouse model of gastric cancer

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel mutations in KvLQT1 that affect Iks activation through interactions with Isk

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic analysis of vertigo 2 Jackson mice with a Kcnq1 potassium channel mutation

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

7 January 2021

based on heuristic

inferred from DOI database lookup

Faecal calprotectin: a novel test for the diagnosis of colorectal cancer?

1 reference

https://api.crossref.org/works/10.1017%2FS1047951112001060

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1017/S1047951112001060

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 August 2017

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