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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

276 related items for PubMed ID: 8179305

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  • 3. A new type of hereditary motor and sensory neuropathy linked to chromosome 3.
    Takashima H, Nakagawa M, Nakahara K, Suehara M, Matsuzaki T, Higuchi I, Higa H, Arimura K, Iwamasa T, Izumo S, Osame M.
    Ann Neurol; 1997 Jun; 41(6):771-80. PubMed ID: 9189038
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  • 4. Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough.
    Miura S, Shibata H, Kida H, Noda K, Tomiyasu K, Yamamoto K, Iwaki A, Ayabe M, Aizawa H, Taniwaki T, Fukumaki Y.
    J Neurol Sci; 2008 Oct 15; 273(1-2):88-92. PubMed ID: 18662816
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  • 8. [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 15; 33(2):175-81. PubMed ID: 8319389
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  • 9. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Feb 15; 31(3-4):207-19. PubMed ID: 8011484
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  • 11. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Electromyogr Clin Neurophysiol; 1998 Mar 15; 38(2):95-101. PubMed ID: 9553747
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  • 12. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD, Ott J, Giblett ER, Chance PF, Sumi SM, Kraft GH.
    Ann Neurol; 1983 Dec 15; 14(6):679-84. PubMed ID: 6651251
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  • 14. [Hereditary neuropathy with liability to pressure palsies].
    Smith TA, Rasmussen K, Hertz JM.
    Ugeskr Laeger; 1999 Jun 07; 161(23):3463-5. PubMed ID: 10388355
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  • 16. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.
    Priest JM, Fischbeck KH, Nouri N, Keats BJ.
    Genomics; 1995 Sep 20; 29(2):409-12. PubMed ID: 8666389
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  • 18. Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.
    Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD.
    Brain; 2005 Dec 20; 128(Pt 12):2797-810. PubMed ID: 16311270
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  • 19. Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathy.
    Gregory R, Thomas PK, King RH, Hallam PL, Malcolm S, Hughes RA, Harding AE.
    Ann Neurol; 1993 Jun 20; 33(6):649-52. PubMed ID: 8498845
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