Landau D, Shalev H, Ohaly M, Carmi R
Infantile variant of Bartter syndrome and sensorineuronal deafness. A new autosomal rezessive
disorder
Am. J. Medi. Genet. 59: 454-459, 1995
Lee WS, Hebert SC
ROMK inwardly rectifying ATP-sensitive K+ channel. I. Expression in rat distal nephron
segments
Am. J. Physiol. 268: F1124-F1131, 1995
Lemmink HH. Heuvel LPWJ van den, Dijk HA van, Merkx GFM, Smilde TJ, Taschner PEM,
Monnens LAH, Hebert SC, Knoers NVAM
Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with
identification of mutations in Dutch families
Pediatr. Nephrol. 10: 403-407, 1996
Leonhardt A, Timmermanns G, Roth B, Seyberth HW
Calcium homeostasis and hypercalciuria in hyperprostaglandin E syndrome
J. Pediatr. 120: 546-554, 1992
López-Nieto CE, Brenner BM
Molecular basis of inherited disorders of renal solute transport
Curr. Opin. Nephrol. Hypert. 6: 411-421, 1997
Lüthy C, Bettinelli A, Iselin S, Metta MG, Basilico E, Oetliker OH, Bianchetti MG
Normal prostaglandinuria E
2
in Gitelman`s syndrome, the hypocalciuric variant of Bartter`s
syndrome
Am. J. Kidney Dis. 25: 824-828, 1995
Mackie FE, Hodson EM, Roy LP, Knight JF
Neonatal Bartter syndrome-use of indomethacin in the newborn period and preservation of
growth failure
Pediatr. Nephrol. 10: 756-758, 1996
Mastroianni N, De Fusco M, Zollo M, Arrigo G, Zuffardi O, Bettinelli A, Ballabio A, Casari G
Molecular cloning, expression pattern and chromosomal localization of the human Na-Cl
thiazide-sensitive cotransporter
Genomics 35: 486-493, 1996a
Komentarze do niniejszej Instrukcji