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Journal Abstract Search

122 related items for PubMed ID: 8538664

  • 21. Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.
    Yurrebaso I, Casado OL, Barcena J, Perez de Nanclares G, Aguirre U.
    Neuromuscul Disord; 2014 Jan; 24(1):56-62. PubMed ID: 24239057
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  • 23. Deletions of chromosome 17p11.2 in multifocal neuropathies.
    Tyson J, Malcolm S, Thomas PK, Harding AE.
    Ann Neurol; 1996 Feb; 39(2):180-6. PubMed ID: 8967749
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  • 24. Molecular basis of hereditary neuropathies.
    Chance PF.
    Phys Med Rehabil Clin N Am; 2001 May; 12(2):277-91. PubMed ID: 11345007
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  • 28. [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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  • 29. Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation.
    Lenssen PP, Gabreëls-Festen AA, Valentijn LJ, Jongen PJ, van Beersum SE, van Engelen BG, van Wensen PJ, Bolhuis PA, Gabreëls FJ, Mariman EC.
    Brain; 1998 Aug 07; 121 ( Pt 8)():1451-8. PubMed ID: 9712007
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  • 33. Hereditary neuropathy with liability to pressure palsies in infancy.
    Goikhman I, Meer J, Zelnik N.
    Pediatr Neurol; 2003 Apr 07; 28(4):307-9. PubMed ID: 12849887
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  • 34. Peripheral nerve biopsy study in 19 cases with 17p11.2 deletion.
    Vital A, Vital C, Latour P, Ferrer X, Rouanet-Larivière M, Brechenmacher C, Lagueny A.
    J Neuropathol Exp Neurol; 2004 Nov 07; 63(11):1167-72. PubMed ID: 15581184
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  • 35. Clinical and neurophysiological findings in patients with hereditary neuropathy with liability to pressure palsy and chromosome 17p11.2 deletion.
    Pabón Meneses RM, Azcona Ganuza G, Urriza Mena J, Ibiricu Yanguas A, Gila Useros L, García de Gurtubay I.
    Neurologia (Engl Ed); 2022 May 07; 37(4):243-249. PubMed ID: 35595399
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  • 37. [Hereditary neuropathy with recurrent mononeuropathy (tomaculous neuropathy)].
    Serena M, Bardin PG.
    Riv Neurol; 1988 May 07; 58(3):97-105. PubMed ID: 3175463
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  • 39. Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy.
    Potulska-Chromik A, Sinkiewicz-Darol E, Ryniewicz B, Lipowska M, Kabzińska D, Kochański A, Kostera-Pruszczyk A.
    Muscle Nerve; 2014 Dec 07; 50(6):914-8. PubMed ID: 24668782
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  • 40. [Molecular genetic diagnosis and clinical features of hereditary neuropathy with liability to pressure palsies in Belarusian patients].
    Asadchuk TV, Rumiantseva NV, Naumchik IV, Likhachev SA, Pleshko IV, Shalkevich LV, Jevneronok IV, Kachan JP.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2016 Dec 07; 116(1):64-69. PubMed ID: 26977628
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