(Q37848047)

24 August 2017

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title

Effect of kidney disease on glucose handling (including genetic defects). (English)

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24 August 2017

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Joaquim Calado

1

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24 August 2017

René Santer

series ordinal

2

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24 August 2017

José Rueff

series ordinal

3

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24 August 2017

José Rueff

series ordinal

4

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24 August 2017

publication date

1 March 2011

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Kidney International. Supplement

24 August 2017

published in

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24 August 2017

issue

120

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24 August 2017

page(s)

S7-13

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The diagnosis of the less common meliturias; including pentosuria and fructosuria

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

https://api.crossref.org/works/10.1038%2FKI.2010.510

1 reference

7 January 2021

Familial renal glycosuria: a genetic reappraisal of hexose transport by kidney and intestine

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

The human kidney low affinity Na+/glucose cotransporter SGLT2. Delineation of the major renal reabsorptive mechanism for D-glucose

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Localization of the Na+/glucose cotransporter gene SGLT2 to human chromosome 16 close to the centromere

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Molecular Analysis of the SGLT2 Gene in Patients with Renal Glucosuria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Renal glucosuria due to SGLT2 mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Active sugar transport in health and disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Close genetic linkage between HLA and renal glycosuria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Dapagliflozin, a novel, selective SGLT2 inhibitor, improved glycemic control over 2 weeks in patients with type 2 diabetes mellitus

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Sodium-glucose cotransport inhibition with dapagliflozin in type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

SGLT2 mediates glucose reabsorption in the early proximal tubule.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Long-term outcome of renal glucosuria type 0: the original patient and his natural history

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Renal Glueosuria and Aminoaciduria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Identification of a novel form of renal glucosuria with overexcretion of arginine, carnosine, and taurine

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuria.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Hypercalciuria in children with renal glycosuria: evidence of dual renal tubular reabsorptive defects

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Fanconi-Bickel syndrome--a congenital defect of facilitative glucose transport

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Molecular basis for glucose-galactose malabsorption

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Dent Disease with mutations in OCRL1

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Physiological roles of CLC Cl(-)/H (+) exchangers in renal proximal tubules

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Absence of ClC5 in knockout mice leads to glycosuria, impaired renal glucose handling and low proximal tubule GLUT2 protein expression.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Mutation of solute carrier SLC16A12 associates with a syndrome combining juvenile cataract with microcornea and renal glucosuria

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Transient Renal Glucosuria in Patients with Tetanus

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Regulatory mechanisms of Na(+)/glucose cotransporters in renal proximal tubule cells.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Maximum Tubular Reabsorption Capacity for Glucose and Renal Hemodynamics during Rapid Hypertonic Glucose Infusion in Normal and Diabetic Subjects

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Changes in facilitative glucose transporter messenger ribonucleic acid levels in the diabetic rat kidney

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Glucose transporters in human renal proximal tubular cells isolated from the urine of patients with non-insulin-dependent diabetes

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Na(+) -glucose transporter-2 messenger ribonucleic acid expression in kidney of diabetic rats correlates with glycemic levels: involvement of hepatocyte nuclear factor-1alpha expression and activity.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Insulin but not phlorizin treatment induces a transient increase in GLUT2 gene expression in the kidney of diabetic rats

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

A low renal threshold for glucose in diabetic patients with a mutation in the hepatocyte nuclear factor-1α (HNF-1α) gene

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

HNF1alpha controls renal glucose reabsorption in mouse and man.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Dapagliflozin, a selective SGLT2 inhibitor, improves glucose homeostasis in normal and diabetic rats

1 reference

https://api.crossref.org/works/10.1038%2FKI.2010.510

7 January 2021

Identifiers

DOI

10.1038/KI.2010.510

1 reference

Dimensions Publication ID

24 August 2017

1025965678

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1 reference