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Journal Abstract Search

183 related items for PubMed ID: 8684395

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. [Clinical features and molecular genetics of autosomal recessive spinocerebellar degenerations].
    Tsuji S.
    Rinsho Shinkeigaku; 2004 Nov; 44(11):785-7. PubMed ID: 15651291
    [Abstract] [Full Text] [Related]

  • 43. Benign hereditary chorea--entity or syndrome?
    Schrag A, Quinn NP, Bhatia KP, Marsden CD.
    Mov Disord; 2000 Mar; 15(2):280-8. PubMed ID: 10752577
    [Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45. Benign hereditary (dominant) chorea of early onset.
    Deonna T, Voumard C.
    Helv Paediatr Acta; 1979 Feb; 34(1):77-83. PubMed ID: 155051
    [Abstract] [Full Text] [Related]

  • 46.
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  • 47. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
    El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F.
    Arch Neurol; 2003 Jul; 60(7):982-8. PubMed ID: 12873855
    [Abstract] [Full Text] [Related]

  • 48. Ataxia with oculomotor apraxia type 2: novel mutations in six patients with juvenile age of onset and elevated serum alpha-fetoprotein.
    Bernard V, Stricker S, Kreuz F, Minnerop M, Gillessen-Kaesbach G, Zühlke C.
    Neuropediatrics; 2008 Dec; 39(6):347-50. PubMed ID: 19569000
    [Abstract] [Full Text] [Related]

  • 49. [Microcephaly with chromosomal instability and immunodeficiency--Nijmegen syndrome].
    Chrzanowska KH.
    Pediatr Pol; 1996 Mar; 71(3):223-34. PubMed ID: 8966094
    [Abstract] [Full Text] [Related]

  • 50. Aprataxin gene mutations in Tunisian families.
    Amouri R, Moreira MC, Zouari M, El Euch G, Barhoumi C, Kefi M, Belal S, Koenig M, Hentati F.
    Neurology; 2004 Sep 14; 63(5):928-9. PubMed ID: 15365154
    [Abstract] [Full Text] [Related]

  • 51. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P, Harrison CJ, Jarosová M, Foroni L.
    Haematologica; 2005 May 14; 90(5):602-11. PubMed ID: 15921375
    [Abstract] [Full Text] [Related]

  • 52. [Benign familial chorea. A not so benign entity].
    Parajua JL, Goñi M, Giménez M, Feijóo M.
    Neurologia; 1989 Nov 14; 4(9):333-5. PubMed ID: 2534715
    [Abstract] [Full Text] [Related]

  • 53. Clinical and genetic heterogeneity in benign hereditary chorea.
    Breedveld GJ, Percy AK, MacDonald ME, de Vries BB, Yapijakis C, Dure LS, Ippel EF, Sandkuijl LA, Heutink P, Arts WF.
    Neurology; 2002 Aug 27; 59(4):579-84. PubMed ID: 12196653
    [Abstract] [Full Text] [Related]

  • 54. Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
    Bauer P, Kreuz FR, Bürk K, Saft C, Andrich J, Heilemann H, Riess O, Schöls L.
    Mov Disord; 2006 Oct 27; 21(10):1734-7. PubMed ID: 16830318
    [Abstract] [Full Text] [Related]

  • 55. [Electrophysiological characteristics of asymptomatic relatives of patients with type 2 spinocerebellar ataxia].
    Velázquez L, Medina EE.
    Rev Neurol; 1998 Dec 27; 27(160):955-63. PubMed ID: 9951012
    [Abstract] [Full Text] [Related]

  • 56. Angelman syndrome: clinical profile.
    Zori RT, Hendrickson J, Woolven S, Whidden EM, Gray B, Williams CA.
    J Child Neurol; 1992 Jul 27; 7(3):270-80. PubMed ID: 1634750
    [Abstract] [Full Text] [Related]

  • 57. [Hereditary ataxia and deafness (Lichtenstein-Knorr disease): study of a family through 5 generations].
    Heras Pérez JA, Asencio Marchante JJ, Ribas Pérez C, Juan-Togores Veguero JM, Portillo Balaguer-Cortés MF.
    Med Clin (Barc); 1986 Oct 18; 87(12):508-9. PubMed ID: 3465984
    [No Abstract] [Full Text] [Related]

  • 58. Ataxia without telangiectasia.
    Friedman JH, Weitberg A.
    Mov Disord; 1993 Apr 18; 8(2):223-6. PubMed ID: 8474496
    [Abstract] [Full Text] [Related]

  • 59. An early-onset recessive cerebellar disorder with distal amyotrophy and, in two patients, gross myoclonia: a probable ataxia telangiectasia variant.
    de Graaf AS, de Jong G, Kleijer WJ.
    Clin Neurol Neurosurg; 1995 Feb 18; 97(1):1-7. PubMed ID: 7788963
    [Abstract] [Full Text] [Related]

  • 60. [Ataxia].
    Dragomir D.
    Pediatrie (Bucur); 1992 Feb 18; 41(4):116-23. PubMed ID: 1335769
    [No Abstract] [Full Text] [Related]

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