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Journal Abstract Search

168 related items for PubMed ID: 1647219

  • 1. Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).
    Weiller C, Ferbert A.
    Eur Arch Psychiatry Clin Neurosci; 1991; 240(4-5):246-9. PubMed ID: 1647219
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  • 3. Leber's optic atrophy: VEP and BAEP changes in 16 asymptomatic subjects.
    Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A.
    Acta Neurol Scand; 1991 Oct; 84(4):366. PubMed ID: 1772010
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  • 4. BAEP changes in Leber's hereditary optic atrophy: further confirmation of multisystem involvement.
    Mondelli M, Rossi A, Scarpini C, Dotti MT, Federico A.
    Acta Neurol Scand; 1990 Apr; 81(4):349-53. PubMed ID: 2360403
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  • 5. Visual and somatosensory evoked potentials in hereditary motor-sensory neuropathies.
    Nevsímalová S, Ponca I, Fiksa J.
    Schweiz Arch Neurol Psychiatr (1985); 1990 Apr; 141(3):217-28. PubMed ID: 1696024
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  • 6. Neurological outcome in 22 treated adolescents with hyperphenylalaninemia. A clinical and electrophysiological study.
    Ludolph AC, Ullrich K, Nedjat S, Masur H, Bick U.
    Acta Neurol Scand; 1992 Apr; 85(4):243-8. PubMed ID: 1316707
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  • 7. Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.
    Chalmers RM, Riordan-Eva P, Wood NW.
    J Neurol Neurosurg Psychiatry; 1997 Apr; 62(4):385-7. PubMed ID: 9120454
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  • 8. Coenzyme Q10 therapy in hereditary motor sensory neuropathy type VI with novel mitofusin 2 mutation.
    Takahashi R, Ikeda T, Hamaguchi A, Iwasa K, Yamada M.
    Intern Med; 2012 Apr; 51(7):791-3. PubMed ID: 22466841
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  • 10. Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.
    Meyer E, Michaelides M, Tee LJ, Robson AG, Rahman F, Pasha S, Luxon LM, Moore AT, Maher ER.
    Mol Vis; 2010 Apr 13; 16():650-64. PubMed ID: 20405026
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  • 11. Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
    Butinar D, Zidar J, Leonardis L, Popovic M, Kalaydjieva L, Angelicheva D, Sininger Y, Keats B, Starr A.
    Ann Neurol; 1999 Jul 13; 46(1):36-44. PubMed ID: 10401778
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  • 12. Hereditary motor and sensory neuropathy type VI with optic atrophy.
    Voo I, Allf BE, Udar N, Silva-Garcia R, Vance J, Small KW.
    Am J Ophthalmol; 2003 Oct 13; 136(4):670-7. PubMed ID: 14516807
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  • 15. Central motor conduction in hereditary motor and sensory neuropathy and hereditary spastic paraplegia.
    Cruz Martínez A, Tejada J.
    Electromyogr Clin Neurophysiol; 1999 Sep 13; 39(6):331-5. PubMed ID: 10499202
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  • 16. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
    Adachi T, Imaoka K, Shirasawa A, Yamaguchi S, Kobayashi S.
    Rinsho Shinkeigaku; 1998 Dec 13; 38(12):1037-41. PubMed ID: 10349345
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  • 17. A multimodal neurophysiological assessment in terminal renal failure.
    Yu YL, Cheng IK, Chang CM, Bruce IC, Mok KY, Zhong WY, Chan YW.
    Acta Neurol Scand; 1991 Feb 13; 83(2):89-95. PubMed ID: 2017903
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  • 18. Peripheral late waves in patients with hereditary motor sensory neuropathy.
    Christova LG, Alexandrov AS, Ishpekova BA.
    Electromyogr Clin Neurophysiol; 1999 Sep 13; 39(6):345-8. PubMed ID: 10499204
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  • 20. [A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].
    Saito T, Nishioka M, Ogino M, Endo K, Kowa H.
    Rinsho Shinkeigaku; 1993 May 13; 33(5):519-24. PubMed ID: 8365058
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