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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

276 related items for PubMed ID: 8179305

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  • 23. [Peroneal muscle atrophy with talipes cavus. Pyramidal symptoms and sensory disorders in one family. On the problem of the nosological classification of hereditary spinal diseases and polyneuropathies].
    Schnider A, Hess CW, Meier C.
    Schweiz Med Wochenschr; 1990 Nov 24; 120(47):1755-62. PubMed ID: 2255880
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  • 24. Central motor conduction in hereditary motor and sensory neuropathy and hereditary spastic paraplegia.
    Cruz Martínez A, Tejada J.
    Electromyogr Clin Neurophysiol; 1999 Sep 24; 39(6):331-5. PubMed ID: 10499202
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  • 25. Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics.
    Elliott JL, Kwon JM, Goodfellow PJ, Yee WC.
    Neurology; 1997 Jan 24; 48(1):23-8. PubMed ID: 9008488
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  • 29. The electrophysiologic profile of Dejerine-Sottas disease (HMSN III).
    Benstead TJ, Kuntz NL, Miller RG, Daube JR.
    Muscle Nerve; 1990 Jul 24; 13(7):586-92. PubMed ID: 2388657
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  • 32. A rare genetic disorder in the differential diagnosis of the entrapment neuropathies: hereditary neuropathy with liability to pressure palsies.
    Koc F, Güzel R, Benlidayi IC, Yerdelen D, Güzel I, Sarica Y.
    J Clin Rheumatol; 2006 Apr 24; 12(2):78-82. PubMed ID: 16601541
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  • 33. A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.
    Muglia M, Patitucci A, Rizzi R, Ungaro C, Conforti FL, Gabriele AL, Magariello A, Mazzei R, Motti L, Sabadini R, Sprovieri T, Marcello N, Quattrone A.
    J Neurol Sci; 2007 Dec 15; 263(1-2):194-7. PubMed ID: 17707409
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  • 34. Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1.
    Roy EP, Gutmann L, Riggs JE.
    Muscle Nerve; 1989 Jan 15; 12(1):52-5. PubMed ID: 2747736
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