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Journal Abstract Search

160 related items for PubMed ID: 7922454

  • 1. Autosomal recessive hereditary sensory neuropathy with spastic paraplegia.
    Thomas PK, Misra VP, King RH, Muddle JR, Wroe S, Bhatia KP, Anderson M, Cabello A, Vilchez J, Wadia NH.
    Brain; 1994 Aug; 117 ( Pt 4)():651-9. PubMed ID: 7922454
    [Abstract] [Full Text] [Related]

  • 2. Hereditary distal dominant amyotrophy followed by spastic paraplegia.
    Sunohara N, Tomi H, Kishibayashi J, Mukoyama M.
    Intern Med; 1993 Nov; 32(11):825-31. PubMed ID: 8012082
    [Abstract] [Full Text] [Related]

  • 3. Hereditary sensory neuropathy with spastic paraplegia.
    Cavanagh NP, Eames RA, Galvin RJ, Brett EM, Kelly RE.
    Brain; 1979 Mar; 102(1):79-94. PubMed ID: 218673
    [Abstract] [Full Text] [Related]

  • 4. Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan Gypsies.
    Thomas PK, Kalaydjieva L, Youl B, Rogers T, Angelicheva D, King RH, Guergueltcheva V, Colomer J, Lupu C, Corches A, Popa G, Merlini L, Shmarov A, Muddle JR, Nourallah M, Tournev I.
    Ann Neurol; 2001 Oct; 50(4):452-7. PubMed ID: 11601496
    [Abstract] [Full Text] [Related]

  • 5. Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.
    Bouhouche A, Benomar A, Bouslam N, Chkili T, Yahyaoui M.
    J Med Genet; 2006 May; 43(5):441-3. PubMed ID: 16399879
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Hereditary motor and sensory neuropathy with spastic paraplegia and optic atrophy: report on a family.
    Dillmann U, Heide G, Dietz B, Teshmar E, Schimrigk K.
    J Neurol; 1997 Sep; 244(9):562-5. PubMed ID: 9352453
    [Abstract] [Full Text] [Related]

  • 8. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V)].
    Murayama T, Nagamatsu M, Sugimura K, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1989 Oct; 29(10):1272-7. PubMed ID: 2691166
    [Abstract] [Full Text] [Related]

  • 9. Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies.
    Colomer J, Iturriaga C, Kalaydjieva L, Angelicheva D, King RH, Thomas PK.
    Neuromuscul Disord; 2000 Dec; 10(8):578-83. PubMed ID: 11053685
    [Abstract] [Full Text] [Related]

  • 10. Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.
    Bouhouche A, Benomar A, Bouslam N, Ouazzani R, Chkili T, Yahyaoui M.
    Eur J Hum Genet; 2006 Feb; 14(2):249-52. PubMed ID: 16333315
    [Abstract] [Full Text] [Related]

  • 11. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
    Kobayashi S, Takuma H, Murayama S, Sakurai M, Kanazawa I.
    J Neurol Sci; 2007 Mar 15; 254(1-2):44-8. PubMed ID: 17258771
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. Giant axonal neuropathy in two siblings: clinical histopathological findings.
    Hergüner MO, Zorludemir S, Altunbasak S.
    Clin Neuropathol; 2005 Mar 15; 24(1):48-50. PubMed ID: 15696785
    [Abstract] [Full Text] [Related]

  • 14. A new variant of sensory ataxic neuropathy with autosomal dominant inheritance.
    van Dijk GW, Wokke JH, Oey PL, Franssen H, Ippel PF, Veldman H.
    Brain; 1995 Dec 15; 118 ( Pt 6)():1557-63. PubMed ID: 8595484
    [Abstract] [Full Text] [Related]

  • 15. Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding in two siblings.
    Barbieri F, Santangelo R, Capparelli G, Ciccarelli A, Crisci C.
    Can J Neurol Sci; 1994 Feb 15; 21(1):29-33. PubMed ID: 8180900
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 114 ( Pt 4)():1855-70. PubMed ID: 1884182
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  • 18. Dejerine-sottas disease with a novel de novo dominant mutation, Ser 149 Arg, of the peripheral myelin protein 22.
    Ohnishi A, Yamamoto T, Izawa K, Yamamori S, Takahashi K, Mega H, Jinnai K.
    Acta Neuropathol; 2000 Mar 15; 99(3):327-30. PubMed ID: 10663978
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  • 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 15; 121 ( Pt 3)():399-408. PubMed ID: 9549516
    [Abstract] [Full Text] [Related]

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