(Q43976045)

28 November 2017

title

Dent's disease and prevalence of renal stones in dialysis patients in Northeastern Italy (English)

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28 November 2017

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Enrica Tosetto

1

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28 November 2017

Romina Graziotto

2

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28 November 2017

Lina Artifoni

3

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28 November 2017

Josef Nachtigal

4

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28 November 2017

Carmelo Cascone

5

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28 November 2017

Piero Conz

6

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28 November 2017

Michele Piva

7

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28 November 2017

Roberto Dell'Aquila

8

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28 November 2017

Ermanno De Paoli Vitali

9

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28 November 2017

Lorenzo Citron

10

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28 November 2017

Federico Nalesso

11

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28 November 2017

Augusto Antonello

12

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28 November 2017

Ugo Vertolli

13

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28 November 2017

Riccardo Zagatti

14

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28 November 2017

Antonio Lupo

15

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28 November 2017

Angela D'Angelo

16

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28 November 2017

Franca Anglani

17

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28 November 2017

Giovanni Gambaro

18

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28 November 2017

publication date

25 October 2005

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Journal of Human Genetics

28 November 2017

published in

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28 November 2017

volume

51

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28 November 2017

issue

1

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28 November 2017

page(s)

25-30

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https://scigraph.springernature.com/pub.10.1007/s10038-005-0317-x

28 November 2017

exact match

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cites work

Dent disease-like phenotype and the chloride channel ClC-4 (CLCN4) gene.

1 reference

12 December 2020

Incidence and management of dialysis patients with renal calculi

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12 December 2020

II. Incidence and prevalence of ESRD

1 reference

12 December 2020

Improved renal function following aggressive treatment of urolithiasis and concurrent mild to moderate renal insufficiency.

1 reference

12 December 2020

Urinary screening of elementary and junior high-school children over a 13-year period in Tokyo.

1 reference

12 December 2020

Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis

1 reference

12 December 2020

Nephrolithiasis: why doesn't our "learning" progress?

1 reference

12 December 2020

ESRD caused by nephrolithiasis: prevalence, mechanisms, and prevention

1 reference

12 December 2020

X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations

1 reference

12 December 2020

Risk for renal failure in nephrolithiasis

1 reference

12 December 2020

A computational analysis of sequence features involved in recognition of short introns

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12 December 2020

Evidence for genetic heterogeneity in Dent's disease

1 reference

12 December 2020

Distribution and characterization of regulatory elements in the human genome

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12 December 2020

Dent Disease with mutations in OCRL1

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12 December 2020

Sequence-based analysis of enzymatically amplified DNA fragments by mutation detection techniques.

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12 December 2020

Causes and consequences of kidney loss in patients with nephrolithiasis

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12 December 2020

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

1 reference

12 December 2020

Dent's disease; a familial proximal renal tubular syndrome with low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, metabolic bone disease, progressive renal failure and a marked male predominance.

1 reference

12 December 2020

Hypercalciuria and nephrocalcinosis in patients with idiopathic low-molecular-weight proteinuria in Japan: is the disease identical to Dent's disease in United Kingdom?

1 reference

12 December 2020

Characterization of carrier females and affected males with X-linked recessive nephrolithiasis

1 reference

12 December 2020

Isolated hypercalciuria with mutation in CLCN5: Relevance to idiopathic hypercalciuria

1 reference

12 December 2020

X-linked recessive nephrolithiasis with renal failure

1 reference

12 December 2020

10.1007/S10038-005-0317-X

Identifiers

DOI

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28 November 2017

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