6 Literaturverzeichnis
Bartter FC, Pronove P, Gill jr. JR, MacCardle RC
Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis.
A new syndrome
Am. J. Med. 33: 811-828, 1962
Bettinelli A, Bianchetti MG, Girardin E, Caringella A, Cecconi M, Appiani AC, Pavanello L,
Gastaldi R, Isimbaldi C, Lama G, Marchesoni C, Matteuci C, Patriarca P, Di Natale B, Setzu C,
Vitucci P
Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic
alkalosis: Bartter and Gitelman syndromes
J. Paediatr. 120: 38-43, 1992
Bettinelli A, Biachetti MG, Borella P, Volpini E, Metta MG, Basilico E, Selicorni A, Bargellini A,
Grassi MR
Genetic heterogeneity in tubular hypomagnesemia-hypokalemia with hypocalciuria (Gitelman`s
syndrome)
Kidney Int. 47: 547-551, 1995
Birkenhäger R, Otto E, Schürmann MJ, Vollmer M, Ruf EM, Maier-Lutz I, Beekmann F, Fekete
A, Omran H, Feldmann D, Milford DV, Jeck N, Konrad M, Landau D, Knoers N, Antignac C,
Sudbrak R, Kispert A, Hildebrandt F
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Nature Gen., 2001
Boim MA, Ho K, Shuck ME, Bienkowski MJ, Block JH, Slightom JL, Yang Y, Brenner BM,
Hebert SC
ROMK inwardly rectifying ATP-sensitive K
+
channel. II. Cloning and distribution of alternative
forms
Am. J. Physiol. 268: F1132-F1140, 1995
Brandt S, Jentsch TJ
ClC-6 and ClC-7 are novel broadly expressed members of the ClC channel family
FEBS Letters 377: 15-20, 1995
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