Acidosis tubular renal

Referencias

Artículos principales

Palmer BF, Kelepouris E, Clegg DJ. Renal tubular acidosis and management strategies: a narrative review. Adv Ther. 2021 Feb;38(2):949-68.Texto completo  Resumen

Kashoor I, Batlle D. Proximal renal tubular acidosis with and without Fanconi syndrome. Kidney Res Clin Pract. 2019 Sep 30;38(3):267-81.Texto completo  Resumen

Giglio S, Montini G, Trepiccione F, et al. Distal renal tubular acidosis: a systematic approach from diagnosis to treatment. J Nephrol. 2021 Mar 26 [online ahead of print].Texto completo  Resumen

Rodriguez Soriano J. Renal tubular acidosis: the clinical entity. J Am Soc Nephrol. 2002 Aug;13(8):2160-70.Texto completo  Resumen

Batlle D, Arruda J. Hyperkalemic forms of renal tubular acidosis: clinical and pathophysiological aspects. Adv Chronic Kidney Dis. 2018 Jul;25(4):321-33. Resumen

Soleimani M, Rastegar A. Pathophysiology of renal tubular acidosis: core curriculum 2016. Am J Kidney Dis. 2016 Sep;68(3):488-98.Texto completo  Resumen

Artículos de referencia

1. Palmer BF, Kelepouris E, Clegg DJ. Renal tubular acidosis and management strategies: a narrative review. Adv Ther. 2021 Feb;38(2):949-68.Texto completo  Resumen

2. Kashoor I, Batlle D. Proximal renal tubular acidosis with and without Fanconi syndrome. Kidney Res Clin Pract. 2019 Sep 30;38(3):267-81.Texto completo  Resumen

3. Giglio S, Montini G, Trepiccione F, et al. Distal renal tubular acidosis: a systematic approach from diagnosis to treatment. J Nephrol. 2021 Mar 26 [online ahead of print].Texto completo  Resumen

4. Rodriguez Soriano J. Renal tubular acidosis: the clinical entity. J Am Soc Nephrol. 2002 Aug;13(8):2160-70.Texto completo  Resumen

5. Alexander RT, Law L, Gil-Peña H, et al. Hereditary distal renal tubular acidosis. In: Adam MP, Ardinger HH, Pagon RA, et al, eds. GeneReviews. Seattle (WA): University of Washington, Seattle; Oct 2019 [internet publication].Texto completo  Resumen

6. Fuster DG, Moe OW. Incomplete distal renal tubular acidosis and kidney stones. Adv Chronic Kidney Dis. 2018 Jul;25(4):366-74. Resumen

7. Foreman JW. Fanconi syndrome. Pediatr Clin North Am. 2019 Feb;66(1):159-67. Resumen

8. Besouw MTP, Bienias M, Walsh P, et al. Clinical and molecular aspects of distal renal tubular acidosis in children. Pediatr Nephrol. 2017 Jun;32(6):987-96. Resumen

9. Tatu CA, Orem WH, Finkelman RB, et al. The etiology of Balkan endemic nephropathy: still more questions than answers. Environ Health Perspect. 1998 Nov;106(11):689-700.Texto completo  Resumen

10. Stefanovic V, Plenakovic M. Fifty years of research in Balkan endemic nephropathy: where are we now? Nephron Clin Pract. 2009;112(2):c51-6.Texto completo  Resumen

11. Nimmannit S, Malasit P, Susaengrat W, et al. Prevalence of endemic distal renal tubular acidosis and renal stone in the northeast of Thailand. Nephron. 1996;72(4):604-10. Resumen

12. Pun KK, Wong CK, Tsui EY, et al. Hypokalemic periodic paralysis due to the Sjögren syndrome in Chinese patients. Ann Intern Med. 1989 Mar 1;110(5):405-6. Resumen

13. Bianic F, Guelfucci F, Robin L, et al. Epidemiology of distal renal tubular acidosis: a study using linked UK primary care and hospital data. Nephron. 2021;145(5):486-95. Resumen

14. Mohebbi N, Wagner CA. Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis. J Nephrol. 2018 Aug;31(4):511-22. Resumen

15. Karet FE. Inherited distal renal tubular acidosis. J Am Soc Nephrol. 2002 Aug;13(8):2178-84.Texto completo  Resumen

16. Elmonem MA, Veys KR, Soliman NA, et al. Cystinosis: a review. Orphanet J Rare Dis. 2016 Apr 22;11:47.Texto completo  Resumen

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18. Palmer BF, Clegg DJ. Hyperchloremic normal gap metabolic acidosis. Minerva Endocrinol. 2019 Dec;44(4):363-77. Resumen

19. Batlle D, Arruda J. Hyperkalemic forms of renal tubular acidosis: clinical and pathophysiological aspects. Adv Chronic Kidney Dis. 2018 Jul;25(4):321-33. Resumen

20. Bello CHPRT, Duarte JS, Vasconcelos C. Diabetes mellitus and hyperkalemic renal tubular acidosis: case reports and literature review. J Bras Nefrol. 2017 Oct-Dec;39(4):481-5.Texto completo  Resumen

21. Schwarz C, Benesch T, Kodras K, et al. Complete renal tubular acidosis late after kidney transplantation. Nephrol Dial Transplant. 2006 Sep;21(9):2615-20.Texto completo  Resumen

22. Kocyigit I, Unal A, Kavuncuoglu F, et al. Renal tubular acidosis in renal transplantation recipients. Ren Fail. 2010 Jul;32(6):687-90. Resumen

23. Online Mendelian Inheritance in Man (OMIM). Fanconi renotubular syndrome 1; FRTS 1: gene map locus 15q15.3. May 2017 [internet publication].Texto completo

24. Patil S, Subramany S, Patil S, et al. Ibuprofen abuse-a case of rhabdomyolysis, hypokalemia, and hypophosphatemia with drug-induced mixed renal tubular acidosis. Kidney Int Rep. 2018 Jun 8;3(5):1237-8.Texto completo  Resumen

25. Ng JL, Morgan DJR, Loh NK, et al. Life-threatening hypokalemia associated with ibuprofen-induced renal tubular acidosis. Med J Aust. 2011 Mar 21;194(6):313-6. Resumen

26. Medland NA, Chow EP, Walker RG, et al. Incidence of renal Fanconi syndrome in patients taking antiretroviral therapy including tenofovir disoproxil fumarate. Int J STD AIDS. 2018 Mar;29(3):227-36. Resumen

27. Palazzo V, Provenzano A, Becherucci F, et al. The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis. Kidney Int. 2017 May;91(5):1243-55. Resumen

28. Watanabe T. Improving outcomes for patients with distal renal tubular acidosis: recent advances and challenges ahead. Pediatric Health Med Ther. 2018 Dec 12;9:181-90.Texto completo  Resumen

29. Alexander RT, Bitzan M. Renal tubular acidosis. Pediatr Clin North Am. 2019 Feb;66(1):135-57. Resumen

30. El Bitar S, Weerasinghe C, El-Charabaty E, et al. Renal tubular acidosis an adverse effect of PD-1 inhibitor immunotherapy. Case Rep Oncol Med. 2018 Jan 31;2018:8408015.Texto completo  Resumen

31. Kaplan MM. Primary biliary cirrhosis. N Engl J Med. 1996 Nov 21;335(21):1570-80. Resumen

32. Haque SK, Ariceta G, Battle G. Proximal renal tubular acidosis: a not so rare disorder of multiple etiologies. Nephrol Dial Transplant. 2012 Dec;27(12):4273-87.Texto completo  Resumen

33. Sly WS, Hewett-Emmett D, Whyte MP, et al. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. Proc Natl Acad Sci U S A. 1983 May;80(9):2752-6. Resumen

34. Sly WS, Whyte MP, Sundaram V, et al. Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. N Engl J Med. 1985 Jul 18;313(3):139-45. Resumen

35. Batlle D, Moorthi KM, Schluter W, et al. Distal renal tubular acidosis and the potassium enigma. Semin Nephrol. 2006 Nov;26(6):471-8. Resumen

36. Karet FE, Finberg KE, Nelson RD, et al: Mutations in the gene encoding the B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness. Nat Genet. 1999 Jan;21(1):84-90. Resumen

37. Smith AN, Skaug J, Choate KA, et al. Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing. Nat Genet. 2000 Sep;26(1):71-5. Resumen

38. Zhang J, Fuster DG, Cameron MA, et al. Incomplete distal renal tubular acidosis from a heterozygous mutation of the V-ATPase B1 subunit. Am J Physiol Renal Physiol. 2014 Nov 1;307(9):F1063-71.Texto completo  Resumen

39. Kurtz I. Renal tubular acidosis: H+/base and ammonia transport abnormalities and clinical syndromes. Adv Chronic Kidney Dis. 2018 Jul;25(4):334-50.Texto completo  Resumen

40. Karet FE, Gainza FJ, Gyory AZ, et al. Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6337-42. Resumen

41. Morris RC Jr. Renal tubular acidosis. Mechanisms, classification and implications. N Engl J Med. 1969 Dec 18;281(25):1405-13. Resumen

42. Igarashi T, Inatomi J, Sekine T, et al. Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities. Nat Genet. 1999 Nov;23(3):264-6. Resumen

43. Bernarado AA, Bernardo CM, Espiritu DJ, et al. The sodium bicarbonate cotransporter: structure, function, and regulation. Semin Nephrol. 2006 Sep;26(5):352-60. Resumen

44. Magen D, Berger L, Coady MJ, et al. A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome. N Engl J Med. 2010 Mar 25;362(12):1102-9.Texto completo  Resumen

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48. Klootwijk ED, Reichold M, Helip-Wooley A, et al. Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome. N Engl J Med. 2014 Jan 9;370(2):129-38. Resumen

49. Sacré A, Jouret F, Manicourt D, et al. Topiramate induces type 3 renal tubular acidosis by inhibiting renal carbonic anhydrase. Nephrol Dial Transplant. 2006 Oct;21(10):2995-6.Texto completo  Resumen

50. Palmer BF. Managing hyperkalemia caused by inhibitors of the renin-angiotensin-aldosterone system. N Engl J Med. 2004 Aug 5;351(6):585-92. Resumen

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53. Lopez-Garcia SC, Emma F, Walsh SB, et al. Treatment and long-term outcome in primary distal renal tubular acidosis. Nephrol Dial Transplant. 2019 Jun 1;34(6):981-91. Resumen

54. Batlle DC, Arruda JA, Kurtzman NA. Hyperkalemic distal renal tubular acidosis associated with obstructive uropathy. N Engl J Med. 1981 Feb 12;304(7):373-80. Resumen

55. Thirakomen K, Kozlov N, Arruda JA, et al. Renal hydrogen ion secretion after release of unilateral ureteral obstruction. Am J Physiol. 1976 Oct;231(4):1233-9. Resumen

56. Hanley MJ, Davidson K. Isolated nephron segments from rabbit models of obstructive nephropathy. J Clin Invest. 1982 Jan;69(1):165-74. Resumen

57. Sabatini S, Kurtzman NA. Enzyme activity in obstructive uropathy: basis for salt wastage and the acidification defect. Kidney Int. 1990 Jan;37(1):79-84. Resumen

58. Sebastian A, Schambelan M, Lindenfeld S, et al. Amelioration of metabolic acidosis with fludrocortisone therapy in hyporeninemic hypoaldosteronism. N Engl J Med. 1977 Sep 15;297(11):576-83. Resumen

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60. Brenner RJ, Spring DB, Sebastian A, et al. Incidence of radiographically evident bone disease, nephrocalcinosis, and nephrolithiasis in various types of renal tubular acidosis. N Engl J Med. 1982 Jul 22;307(4):217-21. Resumen

61. Higashihara E, Nutahara K, Tago K, et al. Medullary sponge kidney and renal acidification defect. Kidney Int. 1984 Feb;25(2):453-9. Resumen

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63. Preminger GM, Sakhaee K, Skurla C, et al. Prevention of recurrent calcium stone formation with potassium citrate therapy in patients with distal renal tubular acidosis. J Urol. 1985 Jul;134(1):20-3. Resumen

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74. Morris RC Jr. An experimental renal acidification defect in patients with hereditary fructose intolerance. II. Its distinction from classic renal tubular acidosis; its resemblance to the renal acidification defect associated with the Fanconi syndrome of children with cystinosis. J Clin Invest. 1968 Jul;47(7):1648-63. Resumen

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109. Jelaković B, Dika Ž, Arlt VM, et al. Balkan endemic nephropathy and the causative role of aristolochic acid. Semin Nephrol. 2019 May;39(3):284-96. Resumen

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131. Soleimani M, Rastegar A. Pathophysiology of renal tubular acidosis: core curriculum 2016. Am J Kidney Dis. 2016 Sep;68(3):488-98.Texto completo  Resumen

132. Halperin ML, Margolis BL, Robinson LA, et al. The urine osmolal gap: a clue to estimate urine ammonium in "hybrid" types of metabolic acidosis. Clin Invest Med. 1988 Jun;11(3):198-202. Resumen

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