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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

140 related items for PubMed ID: 16113197

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  • 2. [A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness].
    Fukuda H, Kitani M, Imaoka K.
    Rinsho Shinkeigaku; 1993 Feb; 33(2):175-81. PubMed ID: 8319389
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  • 3. Laryngeal neuropathy of Charcot-Marie-Tooth disease: further observations and novel mutations associated with vocal fold paresis.
    Benson B, Sulica L, Guss J, Blitzer A.
    Laryngoscope; 2010 Feb; 120(2):291-6. PubMed ID: 19950375
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  • 4. Charcot-Marie-Tooth Disease type 1 and pediatric true vocal fold paralysis.
    Boseley ME, Bloch I, Hartnick CJ.
    Int J Pediatr Otorhinolaryngol; 2006 Feb; 70(2):345-7. PubMed ID: 16084600
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  • 5. [Anesthetic and postoperative management of Charcot-Marie-Tooth disease associated with vocal cord paralysis].
    Watanabe T, Yamashita M, Kondo Y, Sato S, Mizutani T, Watanabe T, Naito H.
    Masui; 1982 May; 31(5):530-4. PubMed ID: 7131729
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  • 8. Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24.
    McEntagart ME, Reid SL, Irrthum A, Douglas JB, Eyre KE, Donaghy MJ, Anderson NE, Rahman N.
    Ann Neurol; 2005 Feb; 57(2):293-7. PubMed ID: 15668982
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  • 10. Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF.
    Gerding WM, Koetting J, Epplen JT, Neusch C.
    Neuromuscul Disord; 2009 Oct; 19(10):701-3. PubMed ID: 19541485
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  • 12. Outcome of vocal cord paralysis in infants.
    Lee CC, Su BH, Lin HC, Tsai YC, Lin CD, Lin TW.
    Acta Paediatr Taiwan; 2004 Oct; 45(5):278-81. PubMed ID: 15868810
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  • 14. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
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  • 15. [Respiratory disorders in type-1 hereditary motor and sensory neuropathy].
    Akiba Y, Kimura T, Kitaoka T, Toyoshima E, Fujiuchi S, Osanai S, Nakano H, Ohsaki Y, Yahara O, Kikuchi K.
    Nihon Kyobu Shikkan Gakkai Zasshi; 1996 Aug; 34(8):850-5. PubMed ID: 8965393
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  • 18. [Midmotoraxonal reexcitation observed in a patient with hereditary motor and sensory neuropathy (HMSN) type IA].
    Hasegawa O, Komiyama A, Kubota-nara Y, Matsumoto S, Kurita R.
    Rinsho Shinkeigaku; 1996 Jan; 36(1):65-7. PubMed ID: 8689795
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