Une cause rare de stagnation pondérale à la naissance : le pseudohypoaldostéronisme de type I-Reference-Cited by-同舟云学术

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Une cause rare de stagnation pondérale à la naissance : le pseudohypoaldostéronisme de type I

Published:2012-05 Issue:5 Volume:19 Page:488-492
ISSN:0929-693X
Container-title:Archives de Pédiatrie
language:fr
Short-container-title:Archives de Pédiatrie

Author:

Derache A.-F.,Rousseau S.,Holder-Espinasse M.,Bouquillon S.,Bresson S.,Ythier H.,Ganga-Zandzou P.-S.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference11 articles.

1. Pleiotropic action of aldosterone in epithelia mediated by transcription and post-transcription mechanisms;Verrey;Kidney Int,2000

2. Mineralocorticoid resistance;Zennaro;Trends Endocrinol Metab,2004

3. Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism;Pujo;Hum Mutat,2007

4. Autosomal dominant pseudohypoaldosteronism type I: mechanisms, evidence for neonatal lethality and phenotypic expression in adults;Geller;J Am Soc Nephrol,2006

5. Pseudohypoaldosteronisms, report on a ten-patient series;Belot;Nephrol Dial Transplant,2008

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1. Hipercalcemia en pacientes con mutación en NR3C2 y SCNN1B;Medicina Clínica;2023-11

2. Hypercalcemia in patients with mutations in NR3C2 and SCNN1B;Medicina Clínica (English Edition);2023-11

3. 30 YEARS OF THE MINERALOCORTICOID RECEPTOR: Mineralocorticoid receptor mutations;Journal of Endocrinology;2017-07

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