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Journal Abstract Search

250 related items for PubMed ID: 18364116

  • 21. Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.
    Wolf MT, Zalewski I, Martin FC, Ruf R, Müller D, Hennies HC, Schwarz S, Panther F, Attanasio M, Acosta HG, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Nieto VG, Hildebrandt F.
    Nephrol Dial Transplant; 2005 May; 20(5):909-14. PubMed ID: 15741201
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  • 24. Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance.
    Finsterer J, Löscher W, Quasthoff S, Wanschitz J, Auer-Grumbach M, Stevanin G.
    J Neurol Sci; 2012 Jul 15; 318(1-2):1-18. PubMed ID: 22554690
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  • 28. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.
    Lossos A, Stevanin G, Meiner V, Argov Z, Bouslam N, Newman JP, Gomori JM, Klebe S, Lerer I, Elleuch N, Silverstein S, Durr A, Abramsky O, Ben-Nariah Z, Brice A.
    Arch Neurol; 2006 May 15; 63(5):756-60. PubMed ID: 16682547
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  • 29. A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q.
    Wang DY, Fan BJ, Chua JK, Tam PO, Leung CK, Lam DS, Pang CP.
    Invest Ophthalmol Vis Sci; 2006 Dec 15; 47(12):5315-21. PubMed ID: 17122119
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  • 31. Spastic paraplegia 15: linkage and clinical description of three Tunisian families.
    Boukhris A, Feki I, Denis E, Miladi MI, Brice A, Mhiri C, Stevanin G.
    Mov Disord; 2008 Feb 15; 23(3):429-33. PubMed ID: 18098276
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  • 32. [Linkage studies of a familial spastic paraplegia pedigree from Tibet].
    Li H, Huang S, Zhu Y, La B, Bai Z, Mu Y, Fischer C, Vogel F, Lo WH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Feb 10; 16(1):5-8. PubMed ID: 9949231
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  • 33. A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.
    Stevanin G, Paternotte C, Coutinho P, Klebe S, Elleuch N, Loureiro JL, Denis E, Cruz VT, Dürr A, Prud'homme JF, Weissenbach J, Brice A, Hazan J.
    Neurology; 2007 May 22; 68(21):1837-40. PubMed ID: 17515546
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  • 34. Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.
    Zhao X, Alvarado D, Rainier S, Lemons R, Hedera P, Weber CH, Tukel T, Apak M, Heiman-Patterson T, Ming L, Bui M, Fink JK.
    Nat Genet; 2001 Nov 22; 29(3):326-31. PubMed ID: 11685207
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  • 35. Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation.
    Fink JK, Hedera P.
    Semin Neurol; 1999 Nov 22; 19(3):301-9. PubMed ID: 12194386
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  • 36. Autosomal dominant hereditary spastic paraplegia with axonal sensory motor polyneuropathy maps to chromosome 21q 22.3.
    Peddareddygari LR, Hanna PA, Igo RP, Luo YA, Won S, Hirano M, Grewal RP.
    Int J Neurosci; 2016 Nov 22; 126(7):600-6. PubMed ID: 26000935
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  • 37. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.
    França MC, D'Abreu A, Maurer-Morelli CV, Seccolin R, Appenzeller S, Alessio A, Damasceno BP, Nucci A, Cendes F, Lopes-Cendes I.
    Mov Disord; 2007 Aug 15; 22(11):1556-62. PubMed ID: 17516453
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  • 39. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.
    Shibasaki Y, Tanaka H, Iwabuchi K, Kawasaki S, Kondo H, Uekawa K, Ueda M, Kamiya T, Katayama Y, Nakamura A, Takashima H, Nakagawa M, Masuda M, Utsumi H, Nakamuro T, Tada K, Kurohara K, Inoue K, Koike F, Sakai T, Tsuji S, Kobayashi H.
    Ann Neurol; 2000 Jul 15; 48(1):108-12. PubMed ID: 10894224
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