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Journal Abstract Search

332 related items for PubMed ID: 15499206

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Transient neonatal cystinuria.
    Boutros M, Vicanek C, Rozen R, Goodyer P.
    Kidney Int; 2005 Feb; 67(2):443-8. PubMed ID: 15673291
    [Abstract] [Full Text] [Related]

  • 3. Molecular genetic analysis of SLC3A1 and SLC7A9 genes in Czech and Slovak cystinuric patients.
    Skopková Z, Hrabincová E, Stástná S, Kozák L, Adam T.
    Ann Hum Genet; 2005 Sep; 69(Pt 5):501-7. PubMed ID: 16138908
    [Abstract] [Full Text] [Related]

  • 4. Clinical and genetic analysis of patients with cystinuria in the United Kingdom.
    Rhodes HL, Yarram-Smith L, Rice SJ, Tabaksert A, Edwards N, Hartley A, Woodward MN, Smithson SL, Tomson C, Welsh GI, Williams M, Thwaites DT, Sayer JA, Coward RJ.
    Clin J Am Soc Nephrol; 2015 Jul 07; 10(7):1235-45. PubMed ID: 25964309
    [Abstract] [Full Text] [Related]

  • 5. A Novel Mutation in SLC3A1 Gene in Patients With Cystinuria.
    Markazi S, Kheirollahi M, Doosti A, Mohammadi M, Koulivand L.
    Iran J Kidney Dis; 2016 Jan 07; 10(1):44-7. PubMed ID: 26837681
    [Abstract] [Full Text] [Related]

  • 6. Twenty-four novel mutations identified in a cohort of 85 patients by direct sequencing of the SLC3A1 and SLC7A9 cystinuria genes.
    Di Perna M, Louizou E, Fischetti L, Dedoussis GV, Stanziale P, Michelakakis H, Zelante L, Pras E, Bisceglia L.
    Genet Test; 2008 Sep 07; 12(3):351-5. PubMed ID: 18752446
    [Abstract] [Full Text] [Related]

  • 7. Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria.
    Yuen YP, Lam CW, Lai CK, Tong SF, Li PS, Tam S, Kwan EY, Chan SY, Tsang WK, Chan KY, Mak WL, Cheng CW, Chan YW.
    Kidney Int; 2006 Jan 07; 69(1):123-8. PubMed ID: 16374432
    [Abstract] [Full Text] [Related]

  • 8. Cystinuria: current diagnosis and management.
    Saravakos P, Kokkinou V, Giannatos E.
    Urology; 2014 Apr 07; 83(4):693-9. PubMed ID: 24246330
    [Abstract] [Full Text] [Related]

  • 9. Digenic Inheritance in Cystinuria Mouse Model.
    Espino M, Font-Llitjós M, Vilches C, Salido E, Prat E, López de Heredia M, Palacín M, Nunes V.
    PLoS One; 2015 Apr 07; 10(9):e0137277. PubMed ID: 26359869
    [Abstract] [Full Text] [Related]

  • 10. An animal model of type A cystinuria due to spontaneous mutation in 129S2/SvPasCrl mice.
    Livrozet M, Vandermeersch S, Mesnard L, Thioulouse E, Jaubert J, Boffa JJ, Haymann JP, Baud L, Bazin D, Daudon M, Letavernier E.
    PLoS One; 2014 Apr 07; 9(7):e102700. PubMed ID: 25048459
    [Abstract] [Full Text] [Related]

  • 11. Cystinuria subtype and the risk of nephrolithiasis.
    Goodyer P, Saadi I, Ong P, Elkas G, Rozen R.
    Kidney Int; 1998 Jul 07; 54(1):56-61. PubMed ID: 9648063
    [Abstract] [Full Text] [Related]

  • 12. Identification of novel cystinuria mutations and polymorphisms in SLC3A1 and SLC7A9 genes: absence of SLC7A10 gene mutations in cystinuric patients.
    Chatzikyriakidou A, Sofikitis N, Georgiou I.
    Genet Test; 2005 Jul 07; 9(3):175-84. PubMed ID: 16225397
    [Abstract] [Full Text] [Related]

  • 13. Mutation analysis of SLC3A1 and SLC7A9 genes in patients with cystinuria.
    Koulivand L, Mohammadi M, Ezatpour B, Salehi R, Markazi S, Dashti S, Kheirollahi M.
    Urolithiasis; 2015 Oct 07; 43(5):447-53. PubMed ID: 26123750
    [Abstract] [Full Text] [Related]

  • 14. In silico analysis of SLC3A1 and SLC7A9 mutations in Iranian patients with Cystinuria.
    Mahdavi M, Koulivand L, Khorrami M, Mirsafaie M, Kheirollahi M.
    Mol Biol Rep; 2018 Oct 07; 45(5):1165-1173. PubMed ID: 30069816
    [Abstract] [Full Text] [Related]

  • 15. [From gene to disease; SLC3A1, SLC7A9 and cystinuria].
    Breuning MH, Hamdy NA.
    Ned Tijdschr Geneeskd; 2003 Feb 08; 147(6):245-7. PubMed ID: 12621979
    [Abstract] [Full Text] [Related]

  • 16. Cystinuria.
    Mattoo A, Goldfarb DS.
    Semin Nephrol; 2008 Mar 08; 28(2):181-91. PubMed ID: 18359399
    [Abstract] [Full Text] [Related]

  • 17. Clinical, biochemical and molecular characterization of cystinuria in a cohort of 12 patients.
    Barbosa M, Lopes A, Mota C, Martins E, Oliveira J, Alves S, De Bonis P, Mota Mdo C, Dias C, Rodrigues-Santos P, Fortuna AM, Quelhas D, Lacerda L, Bisceglia L, Cardoso ML.
    Clin Genet; 2012 Jan 08; 81(1):47-55. PubMed ID: 21255007
    [Abstract] [Full Text] [Related]

  • 18. Delineation of cystinuria in Saudi Arabia: A case series.
    Obaid A, Nashabat M, Al Fakeeh K, Al Qahtani AT, Alfadhel M.
    BMC Nephrol; 2017 Feb 06; 18(1):50. PubMed ID: 28166740
    [Abstract] [Full Text] [Related]

  • 19. A mouse model of type B cystinuria due to spontaneous mutation in FVB/NJcl mice.
    Sasaki H, Sasaki T, Hiura K, Watanabe M, Sasaki N.
    Urolithiasis; 2022 Dec 06; 50(6):679-684. PubMed ID: 35988091
    [Abstract] [Full Text] [Related]

  • 20. SLC3A1 and SLC7A9 mutations in autosomal recessive or dominant canine cystinuria: a new classification system.
    Brons AK, Henthorn PS, Raj K, Fitzgerald CA, Liu J, Sewell AC, Giger U.
    J Vet Intern Med; 2013 Dec 06; 27(6):1400-8. PubMed ID: 24001348
    [Abstract] [Full Text] [Related]

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