Harika Alpay

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

David B. Simon, Ranjit S. Bindra, Traci A. Mansfield et al. · Nature Genetics · 1997 · 863 citations

Channelopathies, Genetic Disorder, Chloride Channel Gene +7

Mutations in the chloride-bicarbonate exchanger gene <i>AE1</i> cause autosomal dominant but not autosomal recessive distal renal tubular acidosis

Fiona E. Karet, Á. Z. Györy, Robert J. Unwin et al. · Proceedings of the National Academy of Sciences · 1998 · 270 citations · Full text

Urology, Renal Function, Dominant Drta +15

Clinical and metabolic features of urolithiasis and microlithiasis in children

Harika Alpay, Ahmet Ozen, İbrahim Gökçe · Pediatric Nephrology · 2009 · 143 citations

Urological Research, Urology, Renal Pathology +4

Etiology of chronic renal failure in Turkish children

Aydan Şirin, Sevinç Emre, Harika Alpay et al. · Pediatric Nephrology · 1995 · 96 citations

Glomerular Disease, Glomerulonephritis, Turkish Children +9

Quality of life in children with chronic kidney disease (with child and parent assessments)

Necla Buyan, Mehmet Türkmen, İlmay Bilge et al. · Pediatric Nephrology · 2010 · 95 citations

Quality Of Life, Hemodialysis, Family Medicine +14