(Q37879992)

24 August 2017

title

Why is hypercalciuria absent at diagnosis in some children with ATP6V1B1 mutation? (English)

1 reference

24 August 2017

Hsin-Yun Tsai

1

1 reference

24 August 2017

Shih-Hua Lin

2

1 reference

24 August 2017

Chun-Chen Lin

3

1 reference

24 August 2017

Fu-Yuan Huang

4

1 reference

24 August 2017

Ming-Dar Lee

5

1 reference

24 August 2017

Jeng-Daw Tsai

6

1 reference

24 August 2017

publication date

26 May 2011

1 reference

24 August 2017

1 reference

24 August 2017

volume

26

1 reference

24 August 2017

issue

10

1 reference

24 August 2017

page(s)

1903-1907

1 reference

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Atypical presentation of distal renal tubular acidosis in two siblings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Inner ear abnormalities in four patients with dRTA and SNHL: clinical and genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Acid-base status determines the renal expression of Ca2+ and Mg2+ transport proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Extracellular pH dynamically controls cell surface delivery of functional TRPV5 channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

The A563T variation of the renal epithelial calcium channel TRPV5 among African Americans enhances calcium influx

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Salt restriction in kidney disease--a missed therapeutic opportunity?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-011-1918-6

Report of a family with two different hereditary diseases leading to early nephrocalcinosis

21 January 2018

1 reference

12 December 2020

Bone mineral density and histology in distal renal tubular acidosis

1 reference

12 December 2020

Normal values for random urinary calcium to creatinine ratios in infancy

1 reference

12 December 2020

Renal histopathology of stone-forming patients with distal renal tubular acidosis

1 reference

12 December 2020

Effect of acute and chronic metabolic acidosis on serum immunoreactive parathyroid hormone in man

1 reference

12 December 2020

10.1007/S00467-011-1918-6

Identifiers

DOI

1 reference

24 August 2017

1 reference