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Journal Abstract Search

165 related items for PubMed ID: 6425198

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  • 3. Red blood cell carbonic anhydrase activity in children with distal renal tubular acidosis.
    Kaplan BS, Mills M, Hechtman P, Leblanc D.
    Pediatr Res; 1977 Oct; 11(10 Pt 1):1039-42. PubMed ID: 409983
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  • 4. Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
    Sly WS, Whyte MP, Sundaram V, Tashian RE, Hewett-Emmett D, Guibaud P, Vainsel M, Baluarte HJ, Gruskin A, Al-Mosawi M.
    N Engl J Med; 1985 Jul 18; 313(3):139-45. PubMed ID: 3925334
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  • 5. Carbonic anhydrase II deficiency in three unrelated Japanese patients.
    Aramaki S, Yoshida I, Yoshino M, Kondo M, Sato Y, Noda K, Jo R, Okue A, Sai N, Yamashita F.
    J Inherit Metab Dis; 1993 Jul 18; 16(6):982-90. PubMed ID: 8127074
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  • 7. Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.
    Kondo T, Taniguchi N, Taniguchi K, Matsuda I, Murao M.
    J Clin Invest; 1978 Sep 18; 62(3):610-7. PubMed ID: 99456
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  • 8. Renal tubular acidosis and deafness: report of a large family.
    Bajaj G, Quan A.
    Am J Kidney Dis; 1996 Jun 18; 27(6):880-2. PubMed ID: 8651253
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  • 9. [Distal renal tubular acidosis with nerve deafness].
    Ronconi GF, Pesenti P, Usai AE, Ronconi M, Soffiati G.
    Pediatr Med Chir; 1984 Jun 18; 6(4):549-52. PubMed ID: 6533602
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  • 16. Carbonic anhydrase II deficiency: diagnosis and carrier detection using differential enzyme inhibition and inactivation.
    Sundaram V, Rumbolo P, Grubb J, Strisciuglio P, Sly WS.
    Am J Hum Genet; 1986 Feb 18; 38(2):125-36. PubMed ID: 3080873
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  • 17. Carbonic anhydrase isoenzyme B in erythrocytes of subjects with chronic acidosis.
    Mondrup M, Anker N.
    Clin Chim Acta; 1979 Mar 15; 92(3):361-6. PubMed ID: 108037
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  • 18. A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.
    Borthwick KJ, Kandemir N, Topaloglu R, Kornak U, Bakkaloglu A, Yordam N, Ozen S, Mocan H, Shah GN, Sly WS, Karet FE.
    J Med Genet; 2003 Feb 15; 40(2):115-21. PubMed ID: 12566520
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