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Journal Abstract Search

112 related items for PubMed ID: 1908057

  • 21. Renal tubular defects in recurring bilateral nephrolithiasis.
    D'Angelo A, Pagano F, Ossi E, Lupo A, Valvo E, Messa P, Tessitore N, Maschio G.
    Clin Nephrol; 1976 Aug; 6(2):352-60. PubMed ID: 954242
    [Abstract] [Full Text] [Related]

  • 22. Clinical features of X-linked nephrolithiasis in childhood.
    Langlois V, Bernard C, Scheinman SJ, Thakker RV, Cox JP, Goodyer PR.
    Pediatr Nephrol; 1998 Oct; 12(8):625-9. PubMed ID: 9811383
    [Abstract] [Full Text] [Related]

  • 23. Familial pure proximal renal tubular acidosis--a clinical and genetic study.
    Katzir Z, Dinour D, Reznik-Wolf H, Nissenkorn A, Holtzman E.
    Nephrol Dial Transplant; 2008 Apr; 23(4):1211-5. PubMed ID: 17881426
    [Abstract] [Full Text] [Related]

  • 24. [X-linked recessively inherited peroneal muscular atrophy].
    Wang DS.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):139-40, 190. PubMed ID: 2591266
    [Abstract] [Full Text] [Related]

  • 25. A common molecular basis for three inherited kidney stone diseases.
    Lloyd SE, Pearce SH, Fisher SE, Steinmeyer K, Schwappach B, Scheinman SJ, Harding B, Bolino A, Devoto M, Goodyer P, Rigden SP, Wrong O, Jentsch TJ, Craig IW, Thakker RV.
    Nature; 1996 Feb 01; 379(6564):445-9. PubMed ID: 8559248
    [Abstract] [Full Text] [Related]

  • 26. Characterization of the peripheral retinopathy in X-linked and autosomal recessive Alport syndrome.
    Shaw EA, Colville D, Wang YY, Zhang KW, Dagher H, Fassett R, Guymer R, Savige J.
    Nephrol Dial Transplant; 2007 Jan 01; 22(1):104-8. PubMed ID: 17071739
    [Abstract] [Full Text] [Related]

  • 27. [Distal renal tubular acidosis and nephrolithiasis in 3 cases of primary Sjögren syndrome].
    Aguilera S, López R, Valdivieso A.
    Rev Med Chil; 1996 Dec 01; 124(12):1467-75. PubMed ID: 9334481
    [Abstract] [Full Text] [Related]

  • 28. Renal tubular dysfunctions in patients with idiopathic calcium nephrolithiasis.
    Pabico RC, McKenna BA, Freeman RB.
    Miner Electrolyte Metab; 1987 Dec 01; 13(6):462-8. PubMed ID: 3696099
    [Abstract] [Full Text] [Related]

  • 29. Ambulatory evaluation of nephrolithiasis: an update of a 1980 protocol.
    Levy FL, Adams-Huet B, Pak CY.
    Am J Med; 1995 Jan 01; 98(1):50-9. PubMed ID: 7825619
    [Abstract] [Full Text] [Related]

  • 30. HIV-associated nephropathy. A unique combined glomerular, tubular, and interstitial lesion.
    Cohen AH, Nast CC.
    Mod Pathol; 1988 Mar 01; 1(2):87-97. PubMed ID: 3070550
    [Abstract] [Full Text] [Related]

  • 31. A family with retinitis pigmentosa and ESRD with late presentation, hypertension and absence of polyuria or salt wasting.
    Friedlaender MM, Rubinger D, Silver J, Zlotogora J, Merin S, Popovtzer MM.
    Clin Nephrol; 1986 Apr 01; 25(4):202-6. PubMed ID: 3698352
    [Abstract] [Full Text] [Related]

  • 32. Familial glomerular disease with asymptomatic proteinuria and nephrotic syndrome: a new clinical entity.
    Mathis BJ, Calabrese KE, Slick GL.
    J Am Osteopath Assoc; 1992 Jul 01; 92(7):875-80, 883-4. PubMed ID: 1429048
    [Abstract] [Full Text] [Related]

  • 33. Familial urate nephropathy.
    Richmond JM, Kincaid-Smith P, Whitworth JA, Becker GJ.
    Clin Nephrol; 1981 Oct 01; 16(4):163-8. PubMed ID: 7296976
    [Abstract] [Full Text] [Related]

  • 34. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance.
    Pochet JM, Bobrie G, Landais P, Goldfarb B, Grünfeld JP.
    Nephrol Dial Transplant; 1989 Oct 01; 4(12):1016-21. PubMed ID: 2517321
    [Abstract] [Full Text] [Related]

  • 35. Chronic renal failure and nephrolithiasis in a solitary kidney: role of intervention.
    Goel MC, Ahlawat R, Kumar M, Kapoor R.
    J Urol; 1997 May 01; 157(5):1574-7. PubMed ID: 9112479
    [Abstract] [Full Text] [Related]

  • 36. Family history may be misleading in the diagnosis of Dent's disease.
    Anglani F, Bernich P, Tosetto E, Cara M, Lupo A, Nalesso F, D'Angelo A, Gambaro G.
    Urol Res; 2006 Feb 01; 34(1):61-3. PubMed ID: 16416111
    [Abstract] [Full Text] [Related]

  • 37. Increased oxidative DNA damage seen in renal biopsies adjacent stones in patients with nephrolithiasis.
    Kittikowit W, Waiwijit U, Boonla C, Ruangvejvorachai P, Pimratana C, Predanon C, Ratchanon S, Tosukhowong P.
    Urolithiasis; 2014 Oct 01; 42(5):387-94. PubMed ID: 25022262
    [Abstract] [Full Text] [Related]

  • 38. Progressive neurologic deterioration and renal failure due to storage of glutamyl ribose-5-phosphate.
    Williams JC, Butler IJ, Rosenberg HS, Verani R, Scott CI, Conley SB.
    N Engl J Med; 1984 Jul 19; 311(3):152-5. PubMed ID: 6738601
    [Abstract] [Full Text] [Related]

  • 39. Dent disease with compound heterozygous mutations leading to severe chronic renal failure in a female patient.
    Holder M, Bald M, Leichter HE, Ludwig M.
    Pediatr Nephrol; 2004 Jan 19; 19(1):122; author reply 123. PubMed ID: 14648329
    [No Abstract] [Full Text] [Related]

  • 40. Nephrolithiasis Associated with Nephrocalcinosis Is Primarily Composed of Carbonate Apatite.
    Kiener TA, Moré E, Franzen M, Cadamuro J, Schwarz C, Bergmann C, Salmhofer H.
    Kidney Blood Press Res; 2024 Jan 19; 49(1):239-244. PubMed ID: 38513628
    [Abstract] [Full Text] [Related]

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