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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

107 related items for PubMed ID: 2665489

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Molecular genetic basis of primary inherited optic neuropathies.
    Votruba M.
    Eye (Lond); 2004 Nov; 18(11):1126-32. PubMed ID: 15534598
    [Abstract] [Full Text] [Related]

  • 23.
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  • 24. The G401D mutation of OPA1 causes autosomal dominant optic atrophy and hearing loss in a Chinese family.
    Ke T, Nie SW, Yang QB, Liu JP, Zhou LN, Ren X, Liu JY, Wang Q, Liu MG.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Oct; 23(5):481-5. PubMed ID: 17029191
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. Leber's hereditary optic neuropathy.
    Letchavanakul A, Dechphongsaphilas W, Dhamcharee V.
    J Med Assoc Thai; 1999 Oct; 82(10):1051-5. PubMed ID: 10561972
    [Abstract] [Full Text] [Related]

  • 27. Bilateral sudden sensorineural hearing loss caused by Charcot-Marie-Tooth disease.
    Papadakis CE, Hajiioannou JK, Kyrmizakis DE, Bizakis JG.
    J Laryngol Otol; 2003 May; 117(5):399-401. PubMed ID: 12803792
    [Abstract] [Full Text] [Related]

  • 28. Dejerine-Sottas syndrome and vestibular loss due to a point mutation in the PMP22 gene.
    Jen J, Baloh RH, Ishiyama A, Baloh RW.
    J Neurol Sci; 2005 Oct 15; 237(1-2):21-4. PubMed ID: 15992829
    [Abstract] [Full Text] [Related]

  • 29. [DNA diagnosis of mitochondrial diseases is now possible].
    Larsson NG, Holme E, Tulinius MH.
    Lakartidningen; 1989 Nov 29; 86(48):4235-6. PubMed ID: 2593758
    [No Abstract] [Full Text] [Related]

  • 30. Hereditary optic neuropathies share a common mitochondrial coupling defect.
    Chevrollier A, Guillet V, Loiseau D, Gueguen N, de Crescenzo MA, Verny C, Ferre M, Dollfus H, Odent S, Milea D, Goizet C, Amati-Bonneau P, Procaccio V, Bonneau D, Reynier P.
    Ann Neurol; 2008 Jun 29; 63(6):794-8. PubMed ID: 18496845
    [Abstract] [Full Text] [Related]

  • 31. [Hereditary optic nerve atrophy. A clinical-genealogical status over Danish families with Leber disease].
    Rosenberg T, Kann E, Nørby S.
    Ugeskr Laeger; 1995 May 08; 157(19):2707-11. PubMed ID: 7770969
    [Abstract] [Full Text] [Related]

  • 32. [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 08; 33(5):519-24. PubMed ID: 8365058
    [Abstract] [Full Text] [Related]

  • 33. Autosomal dominant hereditary sensory neuropathy with chronic cough and gastro-oesophageal reflux: clinical features in two families linked to chromosome 3p22-p24.
    Spring PJ, Kok C, Nicholson GA, Ing AJ, Spies JM, Bassett ML, Cameron J, Kerlin P, Bowler S, Tuck R, Pollard JD.
    Brain; 2005 Dec 08; 128(Pt 12):2797-810. PubMed ID: 16311270
    [Abstract] [Full Text] [Related]

  • 34. [Hereditary neuropathy with recurrent mononeuropathy (tomaculous neuropathy)].
    Serena M, Bardin PG.
    Riv Neurol; 1988 Dec 08; 58(3):97-105. PubMed ID: 3175463
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. Familial spastic paraplegia.
    Phanthumchinda K, Somrealvongkul B.
    J Med Assoc Thai; 1989 Feb 08; 72(2):62-6. PubMed ID: 2738487
    [Abstract] [Full Text] [Related]

  • 37. Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
    Leonardis L, Zidar J, Popovic M, Timmerman V, Löfgren A, Van Broeckhoven C, Butinar D.
    Pflugers Arch; 2000 Feb 08; 439(3 Suppl):R208-10. PubMed ID: 10653194
    [Abstract] [Full Text] [Related]

  • 38. Calcification of the central nervous system in a new hereditary neurological syndrome.
    Reske-Nielsen E, Jensen PK, Hein-Sørensen O, Abelskov K.
    Acta Neuropathol; 1988 Feb 08; 75(6):590-6. PubMed ID: 3376762
    [Abstract] [Full Text] [Related]

  • 39. Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).
    Weiller C, Ferbert A.
    Eur Arch Psychiatry Clin Neurosci; 1991 Feb 08; 240(4-5):246-9. PubMed ID: 1647219
    [Abstract] [Full Text] [Related]

  • 40. [Syndrome of optic nerve atrophy, diabetes mellitus and diabetes insipidus].
    Kolomoĭskaia MB.
    Ter Arkh; 1990 Feb 08; 62(12):90-2. PubMed ID: 2084933
    [Abstract] [Full Text] [Related]

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