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24. Familial proximal renal tubular acidosis. A distinct clinical entity. Brenes LG; Brenes JN; Hernandez MM Am J Med; 1977 Aug; 63(2):244-52. PubMed ID: 888846 [TBL] [Abstract][Full Text] [Related]
25. Osteopetrosis, renal tubular acidosis and basal ganglia calcification in three sisters. Whyte MP; Murphy WA; Fallon MD; Sly WS; Teitelbaum SL; McAlister WH; Avioli LV Am J Med; 1980 Jul; 69(1):64-74. PubMed ID: 7386510 [TBL] [Abstract][Full Text] [Related]
26. Oral administration of sodium bicarbonate to patients with renal tubular acidosis. Shioji R; Sasaki Y; Hurukawa Y; Saito H; Michimata Y Tohoku J Exp Med; 1974 Sep; 114(1):1-13. PubMed ID: 4432240 [No Abstract] [Full Text] [Related]
27. [Renal tubular acidoses in children]. Foulard M Lille Med; 1974 May; 19(5):598-602. PubMed ID: 4431280 [No Abstract] [Full Text] [Related]
28. Distal renal tubular acidosis in children with chronic hydronephrosis. Hutcheon RA; Kaplan BS; Drummond KN J Pediatr; 1976 Sep; 89(3):372-76. PubMed ID: 956961 [TBL] [Abstract][Full Text] [Related]
29. Cerebral calcification, osteopetrosis and renal tubular acidosis: is it carbonic anhydrase-II deficiency? Sh Ali AA; Al-Mashta SA Saudi J Kidney Dis Transpl; 2013 May; 24(3):561-5. PubMed ID: 23640632 [TBL] [Abstract][Full Text] [Related]
31. Carbonic anhydrase II deficiency: a rare autosomal recessive disorder of osteopetrosis, renal tubular acidosis, and cerebral calcification. Cotter M; Connell T; Colhoun E; Smith OP; McMahon C J Pediatr Hematol Oncol; 2005 Feb; 27(2):115-7. PubMed ID: 15701991 [TBL] [Abstract][Full Text] [Related]
32. Renal tubular acidosis and deafness: report of a large family. Bajaj G; Quan A Am J Kidney Dis; 1996 Jun; 27(6):880-2. PubMed ID: 8651253 [TBL] [Abstract][Full Text] [Related]
33. [Carbonic anhydrase II deficiency: osteopetrosis, renal tubular acidosis and intracranial calcifications. Review of the literature and 3 cases]. Cochat P; Loras-Duclaux I; Guibaud P Pediatrie; 1987; 42(2):121-8. PubMed ID: 3112731 [TBL] [Abstract][Full Text] [Related]
35. Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation. Shah GN; Bonapace G; Hu PY; Strisciuglio P; Sly WS Hum Mutat; 2004 Sep; 24(3):272. PubMed ID: 15300855 [TBL] [Abstract][Full Text] [Related]
36. Carbonic anhydrase II deficiency syndrome: recessive osteopetrosis with renal tubular acidosis and cerebral calcification. Ohlsson A; Cumming WA; Paul A; Sly WS Pediatrics; 1986 Mar; 77(3):371-81. PubMed ID: 3081869 [TBL] [Abstract][Full Text] [Related]