Pediatría
Departamento
Hacettepe University
Ankara, TurquíaPublicaciones en colaboración con investigadoras/es de Hacettepe University (6)
2022
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Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study
Nephrology Dialysis Transplantation, Vol. 37, Núm. 12, pp. 2474-2486
2017
2016
2002
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Novel ATP6V1B1 and ATP6V0a4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
Journal of Medical Genetics, Vol. 39, Núm. 11, pp. 796-803
1999
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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness
Nature Genetics, Vol. 21, Núm. 1, pp. 84-90
1997
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Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
Nature Genetics, Vol. 17, Núm. 2, pp. 171-178