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Bartter Disease
Known as:
Hypokalemic Alkalosis
, barters disease
, Bartter's syndrome
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A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA…
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National Institutes of Health
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Related topics
Related topics
24 relations
Narrower (3)
BARTTER SYNDROME, TYPE 4A
Bartter syndrome, antenatal type 1
Bartter syndrome, type 3
Captopril
Dent's disease
Enalapril
Enalapril Maleate
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Broader (3)
Hyperaldosteronism
Syndrome
juxtaglomerular cell hyperplasia
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2001
Highly Cited
2001
Intrarenal and cellular localization of CLC-K2 protein in the mouse kidney.
Katsuki Kobayashi
,
Shinichi Uchida
,
Shuki Mizutani
,
S. Sasaki
,
F. Marumo
Journal of the American Society of Nephrology
2001
Corpus ID: 35162455
CLC-K2, a kidney-specific member of the CLC chloride channel family, is thought to play an important role in the transepithelial…
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Highly Cited
2001
Highly Cited
2001
Pathogenetic role of cyclooxygenase‐2 in hyperprostaglandin E syndrome/antenatal bartter syndrome: Therapeutic use of the cyclooxygenase‐2 inhibitor nimesulide
R. Nüsing
,
S. Reinalter
,
M. Peters
,
M. Kömhoff
,
H. Seyberth
Clinical pharmacology and therapy
2001
Corpus ID: 27482795
Highly Cited
1999
Highly Cited
1999
pH gating of ROMK (K(ir)1.1) channels: control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome.
U. Schulte
,
H. Hahn
,
+7 authors
J. Ludwig
Proceedings of the National Academy of Sciences…
1999
Corpus ID: 10667336
Inward-rectifier K(+) channels of the ROMK (K(ir)1.1) subtype are responsible for K(+) secretion and control of NaCl absorption…
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Highly Cited
1997
Highly Cited
1997
A common NKCC2 mutation in Costa Rican Bartter's syndrome patients: evidence for a founder effect.
C. L. Kurtz
,
L. Károlyi
,
+7 authors
L. Guay-Woodford
Journal of the American Society of Nephrology
1997
Corpus ID: 8022743
Bartter's syndrome involves an overlapping set of closely related renal tubular disorders that can be subdivided into at least…
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Highly Cited
1995
Highly Cited
1995
Possible discrimination of Gitelman's syndrome from Bartter's syndrome by renal clearance study: report of two cases.
T. Tsukamoto
,
Tatsuya Kobayashi
,
Kunihiko Kawamoto
,
Masaaki Fukase
,
Kazuo Chihara
American Journal of Kidney Diseases
1995
Corpus ID: 45322206
Review
1993
Review
1993
The intrarenal renin-angiotensin system.
Kevin D. Burns
,
T. Homma
,
R. Harris
Seminars in Nephrology
1993
Corpus ID: 23268939
In this article, we have discussed the localization of components of the renal renin-angiotensin system, as well as the existing…
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1983
1983
Primary cortisol resistance: a family study.
G. Chrousos
,
A. Vingerhoeds
,
D. Loriaux
,
M. Lipsett
Journal of Clinical Endocrinology and Metabolism
1983
Corpus ID: 41966225
Primary cortisol resistance is an autosomal disease characterized by increased plasma cortisol concentration and high urinary…
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Highly Cited
1980
Highly Cited
1980
Studies on the pathogenesis of Bartter's syndrome.
R. Baehler
,
R. Baehler
,
+7 authors
G. Guthrie
American Journal of Medicine
1980
Corpus ID: 45712266
Highly Cited
1972
Highly Cited
1972
A new male pseudo-hermaphroditism associated with hypertension due to a block of 17 -hydroxylation.
H. Bricaire
,
J. Luton
,
+4 authors
M. Lemmer
Journal of Clinical Endocrinology and Metabolism
1972
Corpus ID: 12993389
ABSTRACT A new 17α-hydroxylase deficiency associated with male pseudohermaphroditism without evidence of puberty and severe…
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Highly Cited
1966
Highly Cited
1966
Desoxycorticosterone Secretion Rates in Hyperadrenocorticism1
M. G. Crane
,
J. J. Harris
1966
Corpus ID: 72177990
Twelve patients with hyperadrenocorticism have been presented, 3 with primary aldosteronism and 9 with Cushing's syndrome. Three…
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