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212 related items for PubMed ID: 1564512

  • 1. Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    J Neurol Sci; 1992 Feb; 107(2):145-54. PubMed ID: 1564512
    [Abstract] [Full Text] [Related]

  • 2.
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  • 3. Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases.
    Schenone A, Abbruzzese M, Uccelli A, Mandich P, James R, Bellone E, Giunchedi M, Rolando S, Capello E, Mandich R [corrected to Mandich P].
    J Neurol Sci; 1994 Mar; 122(1):20-7. PubMed ID: 8195799
    [Abstract] [Full Text] [Related]

  • 4. X-linked dominant hereditary motor and sensory neuropathy.
    Hahn AF, Brown WF, Koopman WJ, Feasby TE.
    Brain; 1990 Oct; 113 ( Pt 5)():1511-25. PubMed ID: 2245309
    [Abstract] [Full Text] [Related]

  • 5. Hereditary motor and sensory neuropathy with calf muscle enlargement.
    Sakashita Y, Sakato S, Komai K, Takamori M.
    J Neurol Sci; 1992 Nov; 113(1):118-22. PubMed ID: 1469450
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  • 6. Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Gooskens RH, Stegeman DF.
    Brain; 1991 Aug; 114 ( Pt 4)():1855-70. PubMed ID: 1884182
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  • 7. Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers.
    Mancardi GL, Di Rocco M, Schenone A, Veneselli E, Doria M, Abbruzzese M, Tabaton M, Borrone C.
    J Neurol Sci; 1992 Jul; 110(1-2):121-30. PubMed ID: 1506851
    [Abstract] [Full Text] [Related]

  • 8. Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.
    Gabreëls-Festen AA, Gabreëls FJ, Hoogendijk JE, Bolhuis PA, Jongen PJ, Vingerhoets HM.
    Acta Neuropathol; 1993 Jul; 86(6):630-5. PubMed ID: 8310819
    [Abstract] [Full Text] [Related]

  • 9. 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; 38(2):95-101. PubMed ID: 9553747
    [Abstract] [Full Text] [Related]

  • 10. The status of HMSN type III.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    Neuromuscul Disord; 1994 Jan; 4(1):63-9. PubMed ID: 8173353
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  • 11. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
    Eirís-Punal J, Vidal-Lijó M, Barros-Angueira F, Lopez-Fernández MJ, Pintos-Martínez E, Beiras-Iglesias A, Castro-Gago M.
    Rev Neurol; 1994 Jan; 31(6):506-10. PubMed ID: 11055050
    [Abstract] [Full Text] [Related]

  • 12. Autosomal recessive form of hereditary motor and sensory neuropathy type I.
    Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Joosten EM, Janssen-van Kempen TW.
    Neurology; 1992 Sep; 42(9):1755-61. PubMed ID: 1513466
    [Abstract] [Full Text] [Related]

  • 13. Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics.
    Elliott JL, Kwon JM, Goodfellow PJ, Yee WC.
    Neurology; 1997 Jan; 48(1):23-8. PubMed ID: 9008488
    [Abstract] [Full Text] [Related]

  • 14. Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III).
    Lynch DR, Hara H, Yum SW, Chance PF, Scherer SS, Bird SJ, Fischbeck KH.
    Neurology; 1997 Aug; 49(2):601-3. PubMed ID: 9270606
    [Abstract] [Full Text] [Related]

  • 15. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C.
    Rom J Neurol Psychiatry; 1993 Aug; 31(3-4):207-19. PubMed ID: 8011484
    [Abstract] [Full Text] [Related]

  • 16. Infantile hereditary neuropathy with hypomyelination: report of two siblings with different expressivity.
    Balestrini MR, Cavaletti G, D'Angelo A, Tredici G.
    Neuropediatrics; 1991 May; 22(2):65-70. PubMed ID: 1857496
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  • 17. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA, McLeod JG, Conchin TE.
    Brain; 1987 Feb; 110 ( Pt 1)():121-48. PubMed ID: 3467805
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  • 19. Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Stegeman DF, Vos AJ, Busch HF.
    Brain; 1990 Dec; 113 ( Pt 6)():1629-43. PubMed ID: 2276038
    [Abstract] [Full Text] [Related]

  • 20. Hereditary motor and sensory neuropathy--Lom, a novel demyelinating neuropathy associated with deafness in gypsies. Clinical, electrophysiological and nerve biopsy findings.
    Kalaydjieva L, Nikolova A, Turnev I, Petrova J, Hristova A, Ishpekova B, Petkova I, Shmarov A, Stancheva S, Middleton L, Merlini L, Trogu A, Muddle JR, King RH, Thomas PK.
    Brain; 1998 Mar; 121 ( Pt 3)():399-408. PubMed ID: 9549516
    [Abstract] [Full Text] [Related]

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