Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

about

Interleukin 18 function in atherosclerosis is mediated by the interleukin 18 receptor and the Na-Cl co-transporter Quadriparesis in diabetes due to dyselectrolytemia.A man with a worrying potassium deficiency

P2860

Q28771509-5B4D2974-AE18-4248-A53C-4E14FB396CB0 Q34714393-FAD570EB-A92F-47D6-A313-E6BB26B2F354 Q38498893-3185777D-9AF8-45C0-81FA-E84BA33ED223

P2860

Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

Item

http://www.wikidata.org/entity/Q43159069

description

2007 nî lūn-bûn

@nan

2007年の論文

@ja

2007年学术文章

@wuu

2007年学术文章

@zh

2007年学术文章

@zh-cn

2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

2007年學術文章

@zh-hant

name

Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

@en

type

Item

label

Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

@en

prefLabel

Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

@en

P1476

Gitelman's syndrome (familial hypokalemia-hypomagnesemia)

@en

P2093

A Gjata

http://www.w3.org/2001/XMLSchema#string

M Gjata

http://www.w3.org/2001/XMLSchema#string

M Tase

http://www.w3.org/2001/XMLSchema#string

Zh Gjergji

http://www.w3.org/2001/XMLSchema#string

P2860

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

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome

A new familial disorder characterized by hypokalemia and hypomagnesemia

Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization

Type IV Bartter syndrome: report of two new cases

Hypomagnesaemia of hereditary renal origin.

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

P304

150-153

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

case report

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2007-07-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

19582211

http://www.w3.org/2001/XMLSchema#string

P932

2658800

http://www.w3.org/2001/XMLSchema#string

Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

about

P2860

P2860

Gitelman's syndrome (familial hypokalemia-hypomagnesemia).

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P577

P698

P932

P1433

P1476

P2093

P2860

P304

P31

P433

P478

P577

P698

P932