Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review.

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Acquired Gitelman syndrome in a primary Sjögren syndrome patient with a SLC12A3 heterozygous mutation: A case report and literature review.

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name

Acquired Gitelman syndrome in ...... report and literature review.

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Acquired Gitelman syndrome in ...... report and literature review.

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Item

label

Acquired Gitelman syndrome in ...... report and literature review.

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Acquired Gitelman syndrome in ...... report and literature review.

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Acquired Gitelman syndrome in ...... report and literature review.

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Acquired Gitelman syndrome in ...... report and literature review.

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P1476

Acquired Gitelman syndrome in ...... e report and literature review

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P2093

Min Chen

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Yanqiu Xu

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Yi Wang

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Zheling Su

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P275

Creative Commons Attribution-NonCommercial-NoDerivatives

P2860

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

A new familial disorder characterized by hypokalemia and hypomagnesemia

Correction of renal hypertension after kidney transplantation from a donor with Gitelman syndrome.

Acquired Gitelman Syndrome in an Anti-SSA Antibody-positive Patient with a SLC12A3 Heterozygous Mutation.

Renal involvement in primary Sjögren syndrome.

Bartter's syndrome. A review of 28 patients followed for 10 years.

Acquired gitelman syndrome

Clinical and morphological features of kidney involvement in primary Sjögren's syndrome.

Primary Sjögren's syndrome associated with Gitelman's syndrome presenting with muscular paralysis.

A novel compound heterozygous mutation of Gitelman's syndrome in Japan, as diagnosed by an extraordinary response of the fractional excretion rate of chloride in the trichlormethiazide loading test.

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652-655

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scholarly article

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10.1111/NEP.13045

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Xiangchen Gu

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ScienceSource

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2017-08-01T00:00:00Z

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28685938

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P921

Gitelman syndrome

Sjögren's syndrome

genetic variation

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6099516

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