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Titolo:
Molecular genetics of renal tubular disorders
Autore:
Hildebrandt, F;
Indirizzi:
Univ Freiburg, Kinderklin, D-79106 Freiburg, Germany Univ Freiburg Freiburg Germany D-79106 erklin, D-79106 Freiburg, Germany
Titolo Testata:
NIEREN-UND HOCHDRUCKKRANKHEITEN
fascicolo: 6, volume: 30, anno: 2001,
pagine: 242 - 260
SICI:
0300-5224(200106)30:6<242:MGORTD>2.0.ZU;2-S
Fonte:
ISI
Lingua:
GER
Soggetto:
BARTTERS-SYNDROME; NA+/GLUCOSE COTRANSPORTER; SENSORINEURAL DEAFNESS; HYPOKALEMIC ALKALOSIS; MUTATIONS; CHANNEL; ACIDOSIS; PROTEIN; SUBUNIT; HETEROGENEITY;
Keywords:
renal tubular disorders; hereditary disorders of renal transport; disease gene identification;
Tipo documento:
Review
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
27
Recensione:
Indirizzi per estratti:
Indirizzo: Hildebrandt, F Univ Freiburg, Kinderklin, Mathildenstr 1, D-79106 Freiburg, Germany Univ Freiburg Mathildenstr 1 Freiburg Germany D-79106 many
Citazione:
F. Hildebrandt, "Molecular genetics of renal tubular disorders", NIEREN HOCH, 30(6), 2001, pp. 242-260

Abstract

In recent years, the identification of disease genes for renal tubular disorders has greatly enhanced the knowledge to the pathophysiology of renal tubular disorders. In this survey, new pathophysiologic insights are described for different tubular segments, together with the classical symptoms that arise from defects of the respective tubular segments.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/04/20 alle ore 04:33:05