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Journal Abstract Search

270 related items for PubMed ID: 18348718

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  • 3. Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review.
    Auer-Grumbach M, De Jonghe P, Verhoeven K, Timmerman V, Wagner K, Hartung HP, Nicholson GA.
    Arch Neurol; 2003 Mar; 60(3):329-34. PubMed ID: 12633143
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  • 6. SPTLC1 and RAB7 mutation analysis in dominantly inherited and idiopathic sensory neuropathies.
    Klein CJ, Wu Y, Kruckeberg KE, Hebbring SJ, Anderson SA, Cunningham JM, Dyck PJ, Klein DM, Thibodeau SN, Dyck PJ.
    J Neurol Neurosurg Psychiatry; 2005 Jul; 76(7):1022-4. PubMed ID: 15965219
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  • 7. Molecular genetics of hereditary sensory neuropathies.
    Auer-Grumbach M, Mauko B, Auer-Grumbach P, Pieber TR.
    Neuromolecular Med; 2006 Jul; 8(1-2):147-58. PubMed ID: 16775373
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  • 9. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations.
    Hilz MJ.
    Clin Auton Res; 2002 May; 12 Suppl 1():I33-43. PubMed ID: 12102461
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  • 13. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I).
    Houlden H, King R, Blake J, Groves M, Love S, Woodward C, Hammans S, Nicoll J, Lennox G, O'Donovan DG, Gabriel C, Thomas PK, Reilly MM.
    Brain; 2006 Feb; 129(Pt 2):411-25. PubMed ID: 16364956
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  • 14. Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.
    Suh BC, Hong YB, Nakhro K, Nam SH, Chung KW, Choi BO.
    Mol Med Rep; 2014 Feb; 9(2):481-6. PubMed ID: 24247255
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  • 16. Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.
    Rotthier A, Baets J, De Vriendt E, Jacobs A, Auer-Grumbach M, Lévy N, Bonello-Palot N, Kilic SS, Weis J, Nascimento A, Swinkels M, Kruyt MC, Jordanova A, De Jonghe P, Timmerman V.
    Brain; 2009 Oct; 132(Pt 10):2699-711. PubMed ID: 19651702
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  • 17. Hereditary perforating ulcers of the foot: "hereditary sensory radicular neuropathy".
    Shahriaree H, Kotcamp WW, Sheikh S, Sajadi K.
    Clin Orthop Relat Res; 1979 May; (140):189-93. PubMed ID: 289445
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  • 18. The N355K atlastin 1 mutation is associated with hereditary sensory neuropathy and pyramidal tract features.
    Leonardis L, Auer-Grumbach M, Papić L, Zidar J.
    Eur J Neurol; 2012 Jul; 19(7):992-8. PubMed ID: 22340599
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  • 19. Mechanisms of disease in hereditary sensory and autonomic neuropathies.
    Rotthier A, Baets J, Timmerman V, Janssens K.
    Nat Rev Neurol; 2012 Jan 24; 8(2):73-85. PubMed ID: 22270030
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  • 20. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan 24; 46(1):1-18. PubMed ID: 16541790
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