Wolf K45E Manual do Utilizador descarregar pdf (Página 118)

Literaturverzeichnis

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111

Jeck N, Reinalter S, Henne T, Marg W, Mallmann R, Pasel K, Vollmer M, Klaus G, Leonhardt A,

Seyberth HW, Konrad M

Hypokalemic salt-losting tubulopathy with chronic renal failure and sensorineuronal deafness

Peditrics 108: E5, 2001a

Jeck N, Derst C, Wischmeyer E, Ott H, Weber S, Rudin C, Seyberth HW, Daut J, Karschin A,

Konrad M

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome

Kidney Intern. 59: 1803-1811, 2001b

Károlyi L, Ziegler A, Pollak M, Fischbach M, Grzeschik KH, Koch MC, Seyberth HW

Gitelman`s syndrome is genetically distinct from other forms of Bartter`s syndrome

Pediatr. Nephrol. 10: 551-554, 1996

Károlyi L, Koch MC, Grzeschik KH, Seyberth HW

The molecular genetic approach to „Bartter`s syndrome“

J. Mol. Med. 76: 317-325, 1998

Kieferle S, Fong P, Bens M, Vandewalle A, Jentsch TJ

Two highly homologous members of the ClC chloride channel family in both rat and human

kidney

Proc. Natl. Acad. Sci. USA 91: 6943-6947, 1994

Köckerling A, Reinalter SC, Seyberth HW

Impaired response to furosemide therapy in hyperprostaglandin E syndrome: Evidence for a

tubular defect in the loop of Henle

J. Pediatr. 129: 519-528, 1996

Köckerling A, Konrad M, Seyberth HW

Hereditäre Salzverlusttubulopathien mit Diurektika-ähnlichem Salzverlust

Dt. Ärzteblatt, Heft 30: A1841-1846, 1998

Konrad M, Vollmer M, Lemmink HH, Van den Heuvel L, Jeck N, Vargas-Poussou R, Lakings A,

Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers N, Seyberth HW, Feldmann D,

Hildebrandt F

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter Syndrome

J. Am. Soc. Nephrol. 11: 1449-1459, 2000

Krishnan SN, Desai T, Ward DC, Haddad GG

Isolation and chromosomal localization of a human ATP-regulated potassium channel

Hum. Genet. 96: 155-160, 1995

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