These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 9452994)

  • 1. X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations.
    Scheinman SJ
    Kidney Int; 1998 Jan; 53(1):3-17. PubMed ID: 9452994
    [No Abstract]   [Full Text] [Related]  

  • 2. Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis.
    Thakker RV
    Kidney Int; 2000 Mar; 57(3):787-93. PubMed ID: 10720930
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ClC-5 chloride channel and kidney stones: what is the link?
    Silva IV; Morales MM; Lopes AG
    Braz J Med Biol Res; 2001 Mar; 34(3):315-23. PubMed ID: 11262581
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
    Scheinman SJ; Cox JP; Lloyd SE; Pearce SH; Salenger PV; Hoopes RR; Bushinsky DA; Wrong O; Asplin JR; Langman CB; Norden AG; Thakker RV
    Kidney Int; 2000 Jan; 57(1):232-9. PubMed ID: 10620204
    [TBL] [Abstract][Full Text] [Related]  

  • 5. CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis.
    Hoopes RR; Hueber PA; Reid RJ; Braden GL; Goodyer PR; Melnyk AR; Midgley JP; Moel DI; Neu AM; VanWhy SK; Scheinman SJ
    Kidney Int; 1998 Sep; 54(3):698-705. PubMed ID: 9734595
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-linked recessive nephrolithiasis: presentation and diagnosis in children.
    Schurman SJ; Norden AG; Scheinman SJ
    J Pediatr; 1998 May; 132(5):859-62. PubMed ID: 9602200
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease.
    Igarashi T; Inatomi J; Ohara T; Kuwahara T; Shimadzu M; Thakker RV
    Kidney Int; 2000 Aug; 58(2):520-7. PubMed ID: 10916075
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular pathology of renal chloride channels in Dent's disease and Bartter's syndrome.
    Thakker RV
    Exp Nephrol; 2000; 8(6):351-60. PubMed ID: 11014932
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CLCN5 mutation Ser244Leu is associated with X-linked renal failure without X-linked recessive hypophosphatemic rickets.
    Kelleher CL; Buckalew VM; Frederickson ED; Rhodes DJ; Conner DA; Seidman JG; Seidman CE
    Kidney Int; 1998 Jan; 53(1):31-7. PubMed ID: 9452997
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new approach to mRNA in proximal tubule cells of patients with CLCN5 channelopathy.
    Morimoto T; Chiba A; Kondo Y; Takahashi S; Igarashi T; Inoue CN; Iinuma K
    Pediatr Nephrol; 2001 Feb; 16(2):110-2. PubMed ID: 11261675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
    Igarashi T; Günther W; Sekine T; Inatomi J; Shiraga H; Takahashi S; Suzuki J; Tsuru N; Yanagihara T; Shimazu M; Jentsch TJ; Thakker RV
    Kidney Int; 1998 Dec; 54(6):1850-6. PubMed ID: 9853249
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic causes of hypercalciuric nephrolithiasis.
    Stechman MJ; Loh NY; Thakker RV
    Pediatr Nephrol; 2009 Dec; 24(12):2321-32. PubMed ID: 18446382
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Medical genetics. Crystal-clear chloride channels.
    Hebert SC
    Nature; 1996 Feb; 379(6564):398-9. PubMed ID: 8559242
    [No Abstract]   [Full Text] [Related]  

  • 14. Molecular and clinical studies of Dent's disease in Japan: biochemical examination and renal ultrasonography do not predict carrier state.
    Matsuyama T; Awazu M; Oikawa T; Inatomi J; Sekine T; Igarashi T
    Clin Nephrol; 2004 Apr; 61(4):231-7. PubMed ID: 15125028
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dietary salt and renal stone disease.
    Devuyst O
    Lancet; 1997 Feb; 349(9050):507. PubMed ID: 9040605
    [No Abstract]   [Full Text] [Related]  

  • 16. [Dent's disease: hereditary nephrolithiasis related to defective tubular endocytosis processes].
    Tosetto E; Anglani F; Graziotto R; Citron L; D'Angelo A; Gambaro G
    G Ital Nefrol; 2003; 20(6):578-88. PubMed ID: 14732909
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 379(6564):445-9. PubMed ID: 8559248
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Making a "dent" in hereditary hypercalciuric nephrolithiasis.
    Stapleton FB
    J Pediatr; 1998 May; 132(5):764-5. PubMed ID: 9602182
    [No Abstract]   [Full Text] [Related]  

  • 19. Dent's disease--a nephrolithiasis disorder associated with defective receptor-mediated endocytosis.
    Thakker R
    Bull Mem Acad R Med Belg; 2004; 159(Pt 2):199-211. PubMed ID: 15615094
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
    Lloyd SE; Gunther W; Pearce SH; Thomson A; Bianchi ML; Bosio M; Craig IW; Fisher SE; Scheinman SJ; Wrong O; Jentsch TJ; Thakker RV
    Hum Mol Genet; 1997 Aug; 6(8):1233-9. PubMed ID: 9259268
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.