Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic

about

Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic

Item

http://www.wikidata.org/entity/Q57646454

description

scientific article published on 30 January 2018

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в серпні 2018

@uk

name

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@en

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@nl

type

Item

label

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@en

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@nl

prefLabel

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@en

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@nl

P1476

Exocrine pancreatic dysfunctio ...... disease and can be symptomatic

@en

P2093

Beverley M Shields

http://www.w3.org/2001/XMLSchema#string

Coralie Bingham

http://www.w3.org/2001/XMLSchema#string

Jon Fulford

http://www.w3.org/2001/XMLSchema#string

Rhian L Clissold

http://www.w3.org/2001/XMLSchema#string

P2860

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study

Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease

Faecal elastase 1: a novel, highly sensitive, and specific tubeless pancreatic function test

Renal cysts and diabetes syndrome linked to mutations of the hepatocyte nuclear factor-1 beta gene: description of a new family with associated liver involvement.

Fecal pancreatic elastase-1 levels in older individuals without known gastrointestinal diseases or diabetes mellitus.

A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta.

Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation.

Urine C-peptide creatinine ratio is a noninvasive alternative to the mixed-meal tolerance test in children and adults with type 1 diabetes.

HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.

HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.

P304

453-458

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1093/CKJ/SFX150

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Andrew Tym Hattersley

Timothy J McDonald

Sian Ellard

Michelle Hudson

P577

2018-01-30T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

30094008

http://www.w3.org/2001/XMLSchema#string

P921

nephrology

P932

6070112

http://www.w3.org/2001/XMLSchema#string