Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

168 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.
Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP. Simon DB, et al. Nat Genet. 1997 Oct;17(2):171-8. doi: 10.1038/ng1097-171. Nat Genet. 1997. PMID: 9326936
Essential fatty acid deficiency profile in patients with nephrotic-range proteinuria.
Aldámiz-Echevarría L, Vallo A, Aguirre M, Sanjurjo P, Gonzalez-Lamuño D, Elorz J, Prieto JA, Andrade F, Rodríguez-Soriano J. Aldámiz-Echevarría L, et al. Among authors: rodriguez soriano j. Pediatr Nephrol. 2007 Apr;22(4):533-40. doi: 10.1007/s00467-006-0366-1. Epub 2006 Nov 23. Pediatr Nephrol. 2007. PMID: 17123116
168 results