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Journal Abstract Search

176 related items for PubMed ID: 14706470

  • 1.
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  • 2. Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease.
    Gutierrez A, England JD, Sumner AJ, Ferer S, Warner LE, Lupski JR, Garcia CA.
    Muscle Nerve; 2000 Feb; 23(2):182-8. PubMed ID: 10639608
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  • 3. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.
    Birouk N, LeGuern E, Maisonobe T, Rouger H, Gouider R, Tardieu S, Gugenheim M, Routon MC, Léger JM, Agid Y, Brice A, Bouche P.
    Neurology; 1998 Apr; 50(4):1074-82. PubMed ID: 9566397
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  • 4. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families.
    Nicholson G, Nash J.
    Neurology; 1993 Dec; 43(12):2558-64. PubMed ID: 8255457
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  • 5. Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1.
    Kaku DA, Parry GJ, Malamut R, Lupski JR, Garcia CA.
    Neurology; 1993 Dec; 43(12):2664-7. PubMed ID: 8255473
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  • 6. Hypertrophic Charcot-Marie-Tooth disease. Light and electron microscope studies of the sural nerve.
    Low PA, McLeod JG, Prineas JW.
    J Neurol Sci; 1978 Jan; 35(1):93-115. PubMed ID: 624962
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  • 7. Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes.
    Bai Y, Ianokova E, Pu Q, Ghandour K, Levinson R, Martin JJ, Ceuterick-de Groote C, Mazanec R, Seeman P, Shy ME, Li J.
    Arch Neurol; 2006 Dec; 63(12):1787-94. PubMed ID: 17172621
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  • 8. [Subclinical lesions of peripheral nervous system in multiple sclerosis patients].
    Pogorzelski R, Baniukiewicz E, Drozdowski W.
    Neurol Neurochir Pol; 2004 Dec; 38(4):257-64. PubMed ID: 15383952
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  • 9. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG, Low PA.
    Clin Exp Neurol; 1977 Dec; 14():142-53. PubMed ID: 616594
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  • 10. Sensory action potentials and biopsy of the sural nerve in neuropathy.
    Behse F, Buchthal.
    Brain; 1978 Sep; 101(3):473-93. PubMed ID: 213163
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  • 11. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
    Berciano J, García A, Gallardo E, Peeters K, Pelayo-Negro AL, Álvarez-Paradelo S, Gazulla J, Martínez-Tames M, Infante J, Jordanova A.
    J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294
    [Abstract] [Full Text] [Related]

  • 12. Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.
    Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G, Study Group for Hereditary Neuropathy in Japan.
    Brain; 2003 Jan; 126(Pt 1):134-51. PubMed ID: 12477701
    [Abstract] [Full Text] [Related]

  • 13. A cohort study of Han Chinese MFN2-related Charcot-Marie-Tooth 2A.
    Lv H, Wang L, Zhang W, Wang Z, Zuo Y, Liu J, Yuan Y.
    J Neurol Sci; 2015 Nov 15; 358(1-2):153-7. PubMed ID: 26382835
    [Abstract] [Full Text] [Related]

  • 14. Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
    Claeys KG, Züchner S, Kennerson M, Berciano J, Garcia A, Verhoeven K, Storey E, Merory JR, Bienfait HM, Lammens M, Nelis E, Baets J, De Vriendt E, Berneman ZN, De Veuster I, Vance JM, Nicholson G, Timmerman V, De Jonghe P.
    Brain; 2009 Jul 15; 132(Pt 7):1741-52. PubMed ID: 19502294
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  • 17. Transthyretin amyloid polyneuropathies mimicking a demyelinating polyneuropathy.
    Lozeron P, Mariani LL, Dodet P, Beaudonnet G, Théaudin M, Adam C, Arnulf B, Adams D.
    Neurology; 2018 Jul 10; 91(2):e143-e152. PubMed ID: 29907605
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