Molecular pathogenesis of Bartter's and Gitelman's syndromes

被引:82
作者
Kurtz, I [1 ]
机构
[1] Univ Calif Los Angeles, Div Nephrol, Sch Med, Los Angeles, CA 90095 USA
关键词
metabolic alkalosis; hyperprostaglandin E syndrome; hypokalemia; hypomagnesemia; hypocalciuria; nephrocalcinosis;
D O I
10.1046/j.1523-1755.1998.00124.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:1396 / 1410
页数:15
相关论文
共 151 条
[51]   LOCALIZATION OF A GENE FOR CHONDROCALCINOSIS TO CHROMOSOME 5P [J].
HUGHES, AE ;
MCGIBBON, D ;
WOODWARD, E ;
DIXEY, J ;
DOHERTY, M .
HUMAN MOLECULAR GENETICS, 1995, 4 (07) :1225-1228
[52]   CLONING, EMBRYONIC EXPRESSION, AND ALTERNATIVE SPLICING OF A MURINE KIDNEY-SPECIFIC NA-K-CL COTRANSPORTER [J].
IGARASHI, P ;
HEUVEL, GBV ;
PAYNE, JA ;
FORBUSH, B .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1995, 269 (03) :F405-F418
[53]   BARTTER SYNDROME - TYPICAL FACIES AND NORMAL PLASMA-VOLUME [J].
JAMES, T ;
HOLLAND, NH ;
PRESTON, D .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1975, 129 (10) :1205-1207
[54]   Chloride channels: An emerging molecular picture [J].
Jentsch, TJ ;
Gunther, W .
BIOESSAYS, 1997, 19 (02) :117-126
[55]   PRIMARY STRUCTURE OF TORPEDO-MARMORATA CHLORIDE CHANNEL ISOLATED BY EXPRESSION CLONING IN XENOPUS OOCYTES [J].
JENTSCH, TJ ;
STEINMEYER, K ;
SCHWARZ, G .
NATURE, 1990, 348 (6301) :510-514
[56]   Prostaglandin E(2) inhibits Na-K-2Cl cotransport in medullary thick ascending limb cells [J].
Kaji, DM ;
Chase, HS ;
Eng, JP ;
Diaz, J .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (01) :C354-C361
[57]   Apical localization of the Na-K-Cl cotransporter, rBSC1, on rat thick ascending limbs [J].
Kaplan, MR ;
Plotkin, MD ;
Lee, WS ;
Xu, ZC ;
Lytton, J ;
Hebert, SC .
KIDNEY INTERNATIONAL, 1996, 49 (01) :40-47
[58]   Molecular mechanisms of NaCl cotransport [J].
Kaplan, MR ;
Mount, DB ;
Delpire, E ;
Gamba, G ;
Hebert, SC .
ANNUAL REVIEW OF PHYSIOLOGY, 1996, 58 :649-668
[59]  
Karolyi L, 1997, HUM MOL GENET, V6, P17
[60]   Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome [J].
Karolyi, L ;
Ziegler, A ;
Pollak, M ;
Fischbach, M ;
Grzeschik, KH ;
Koch, MC ;
Seyberth, HW .
PEDIATRIC NEPHROLOGY, 1996, 10 (05) :551-554