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Journal Abstract Search

401 related items for PubMed ID: 3829750

  • 1. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).
    Chan CK, Mohsenin V, Loke J, Virgulto J, Sipski ML, Ferranti R.
    Chest; 1987 Apr; 91(4):567-70. PubMed ID: 3829750
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  • 3. Charcot-Marie-Tooth disease with diaphragmatic weakness.
    Osanai S, Akiba Y, Nakano H, Matsumoto H, Yahara O, Onodera S.
    Intern Med; 1992 Nov; 31(11):1267-70. PubMed ID: 1295621
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  • 4. Phrenic nerve involvement and respiratory muscle weakness in patients with Charcot-Marie-Tooth disease 1A.
    Spiesshoefer J, Henke C, Kabitz HJ, Akova-Oeztuerk E, Draeger B, Herkenrath S, Randerath W, Young P, Brix T, Boentert M.
    J Peripher Nerv Syst; 2019 Sep; 24(3):283-293. PubMed ID: 31393643
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  • 11. Ataxia and other data reviewed in Charcot-Marie-Tooth and Refsum's disease.
    Salisachs P.
    J Neurol Neurosurg Psychiatry; 1982 Dec; 45(12):1085-91. PubMed ID: 6186770
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  • 12. Diaphragm weakness in Charcot-Marie-Tooth disease.
    Laroche CM, Carroll N, Moxham J, Stanley NN, Evans RJ, Green M.
    Thorax; 1988 Jun; 43(6):478-9. PubMed ID: 3420560
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  • 13. Unilateral oculomotor palsy in Charcot-Marie-Tooth disease 1A (CMT 1A).
    Posa A, Emmer A, Kornhuber ME.
    Clin Neurol Neurosurg; 2017 Apr; 155():20-21. PubMed ID: 28214652
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  • 15. Laryngeal electromyographic findings in Charcot-Marie-Tooth disease type II.
    Dray TG, Robinson LR, Hillel AD.
    Arch Neurol; 1999 Jul; 56(7):863-5. PubMed ID: 10404989
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  • 16. Phenotypic convergence in Charcot-Marie-Tooth 2Y with novel VCP mutation.
    Gite J, Milko E, Brady L, Baker SK.
    Neuromuscul Disord; 2020 Mar; 30(3):232-235. PubMed ID: 32165109
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  • 17. Phenotype of Charcot-Marie-Tooth disease Type 2.
    Bienfait HM, Baas F, Koelman JH, de Haan RJ, van Engelen BG, Gabreëls-Festen AA, Ongerboer de Visser BW, Meggouh F, Weterman MA, De Jonghe P, Timmerman V, de Visser M.
    Neurology; 2007 May 15; 68(20):1658-67. PubMed ID: 17502546
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  • 19. Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case.
    Kulshrestha R, Forrester N, Antoniadi T, Willis T, Sethuraman SK, Samuels M.
    Neuromuscul Disord; 2018 Dec 15; 28(12):1016-1021. PubMed ID: 30409445
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