Tubular and genetic disorders associated with kidney stones (Q39023120)

8 September 2017

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title

Tubular and genetic disorders associated with kidney stones (English)

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8 September 2017

1

Nilufar Mohebbi

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8 September 2017

author name string

Pietro Manuel Ferraro

series ordinal

2

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8 September 2017

Giovanni Gambaro

series ordinal

3

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8 September 2017

Robert Unwin

series ordinal

4

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8 September 2017

publication date

28 November 2016

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8 September 2017

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8 September 2017

volume

45

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8 September 2017

issue

1

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8 September 2017

page(s)

127-137

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Prevalence of kidney stones in the United States

8 September 2017

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21 January 2018

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21 January 2018

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12 December 2020

The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type III

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12 December 2020

Combined liver-kidney transplantation for hyperoxaluria type II?

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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.

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The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3

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12 December 2020

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12 December 2020

Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria

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12 December 2020

10.1007/S00240-016-0945-Y

Identifiers

DOI

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8 September 2017

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