These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

221 related items for PubMed ID: 9120454

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.
    Chalmers RM, Bird AC, Harding AE.
    J Neurol Neurosurg Psychiatry; 1996 Feb; 60(2):195-6. PubMed ID: 8708653
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy.
    Thomas PK, Claus D, King RH.
    J Neurol; 1999 Feb; 246(2):107-12. PubMed ID: 10195405
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
    Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, Hamilton SR, Van Stavern G, Krajewski KM, Stajich J, Tournev I, Verhoeven K, Langerhorst CT, de Visser M, Baas F, Bird T, Timmerman V, Shy M, Vance JM.
    Ann Neurol; 2006 Feb; 59(2):276-81. PubMed ID: 16437557
    [Abstract] [Full Text] [Related]

  • 6. New form of autosomal-recessive axonal hereditary sensory motor neuropathy.
    Eckhardt SM, Hicks EM, Herron B, Morrison PJ, Aicardi J.
    Pediatr Neurol; 1998 Sep; 19(3):234-5. PubMed ID: 9806145
    [Abstract] [Full Text] [Related]

  • 7. Autosomal dominant HMSN with proximal involvement: new Brazilian cases.
    Patroclo CB, Lino AM, Marchiori PE, Brotto MW, Hirata MT.
    Arq Neuropsiquiatr; 2009 Sep; 67(3B):892-6. PubMed ID: 19838524
    [Abstract] [Full Text] [Related]

  • 8. 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; 136(4):670-7. PubMed ID: 14516807
    [Abstract] [Full Text] [Related]

  • 9. Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.
    MacDermot KD, Walker RW.
    J Neurol Neurosurg Psychiatry; 1987 Oct; 50(10):1342-7. PubMed ID: 3479531
    [Abstract] [Full Text] [Related]

  • 10. Hereditary motor and sensory neuropathy with congenital glaucoma. Report on a family.
    Arruda WO, Comerlato EA, Scola RH, Silvado CE, Werneck LC.
    Arq Neuropsiquiatr; 1999 Jun; 57(2A):190-4. PubMed ID: 10412516
    [Abstract] [Full Text] [Related]

  • 11. Proximal Dominant Hereditary Motor and Sensory Neuropathy with TFG Mutation: First Case Report from India.
    Ansari AF, Jagiasi K, Ojha P, Ansari R, Nagendra S, Kharat S.
    Neurol India; 2022 Jun; 70(3):1220-1222. PubMed ID: 35864671
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis.
    Dyck PJ, Litchy WJ, Minnerath S, Bird TD, Chance PF, Schaid DJ, Aronson AE.
    Ann Neurol; 1994 May; 35(5):608-15. PubMed ID: 8179305
    [Abstract] [Full Text] [Related]

  • 14. Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1.
    Lee J, Jung SC, Hong YB, Yoo JH, Koo H, Lee JH, Hong HD, Kim SB, Chung KW, Choi BO.
    Mol Med Rep; 2016 Jul; 14(1):33-40. PubMed ID: 27150940
    [Abstract] [Full Text] [Related]

  • 15. Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait.
    Tolmie JL, Wilcox DE, McWilliam R, Assindi A, Stephenson JB.
    J Med Genet; 1988 Nov; 25(11):754-7. PubMed ID: 2976839
    [Abstract] [Full Text] [Related]

  • 16. TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophy.
    Désir J, Coppieters F, Van Regemorter N, De Baere E, Abramowicz M, Cordonnier M.
    Mol Vis; 2012 Nov; 18():1849-57. PubMed ID: 22815638
    [Abstract] [Full Text] [Related]

  • 17. [A case of hereditary motor and sensory neuropathy (HMSN) with excessive myelin outfolding with autosomal recessive inheritance].
    Ohnishi A, Narazaki O, Hanai T.
    J UOEH; 1998 Dec 01; 20(4):345-52. PubMed ID: 9883484
    [Abstract] [Full Text] [Related]

  • 18. Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma.
    Kiwaki T, Umehara F, Takashima H, Nakagawa M, Kamimura K, Kashio N, Sakamoto Y, Unoki K, Nobuhara Y, Michizono K, Watanabe O, Arimura H, Osame M.
    Neurology; 2000 Aug 08; 55(3):392-7. PubMed ID: 10932274
    [Abstract] [Full Text] [Related]

  • 19. Homozygous hypertrophic hereditary motor and sensory neuropathies.
    Sghirlanzoni A, Pareyson D, Marazzi R, Cavaletti G, Bellone E, Mandich P, Balestrini MR, Riva D.
    Ital J Neurol Sci; 1994 Feb 08; 15(1):5-14. PubMed ID: 8206746
    [Abstract] [Full Text] [Related]

  • 20. 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 08; 107(2):145-54. PubMed ID: 1564512
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.