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Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrheaSlc26a3/Dra and Slc26a6 in Murine Ameloblasts.Review article: the clinical management of congenital chloride diarrhoea.Update on SLC26A3 mutations in congenital chloride diarrhea.Oral butyrate in treatment of congenital chloride diarrhea.A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR.Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability.The impact of sodium chloride and volume depletion in the chronic kidney disease of congenital chloride diarrheaFollow-up of a child with congenital chloride diarrhoea caused by a novel mutationCongenital chloride diarrhea misdiagnosed as Bartter syndrome
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-0212-4851
@en
name
Satu Wedenoja
@ast
Satu Wedenoja
@en
Satu Wedenoja
@es
Satu Wedenoja
@nl
type
label
Satu Wedenoja
@ast
Satu Wedenoja
@en
Satu Wedenoja
@es
Satu Wedenoja
@nl
prefLabel
Satu Wedenoja
@ast
Satu Wedenoja
@en
Satu Wedenoja
@es
Satu Wedenoja
@nl
P106
P31
P496
0000-0003-0212-4851