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PUBMED FOR HANDHELDS

Journal Abstract Search


197 related items for PubMed ID: 7614093

  • 1. Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.
    Belal S, Hentati F, Ben Hamida C, Ben Hamida M.
    Clin Neurosci; 1995; 3(1):39-42. PubMed ID: 7614093
    [Abstract] [Full Text] [Related]

  • 2. Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.
    Marzouki N, Benomar A, Yahyaoui M, Birouk N, Elouazzani M, Chkili T, Benlemlih M.
    Eur J Med Genet; 2005; 48(1):21-8. PubMed ID: 15953402
    [Abstract] [Full Text] [Related]

  • 3. [Friedreich's ataxia and hereditary vitamin E deficiency. Case study].
    Labauge P, Cavalier L, Ichalalène L, Castelnovo G.
    Rev Neurol (Paris); 1998 May; 154(4):339-41. PubMed ID: 9773063
    [Abstract] [Full Text] [Related]

  • 4. Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families.
    Ben Hamida M, Belal S, Sirugo G, Ben Hamida C, Panayides K, Ionannou P, Beckmann J, Mandel JL, Hentati F, Koenig M.
    Neurology; 1993 Nov; 43(11):2179-83. PubMed ID: 8232925
    [Abstract] [Full Text] [Related]

  • 5. Friedreich ataxia.
    Johnson WG.
    Clin Neurosci; 1995 Nov; 3(1):33-8. PubMed ID: 7614092
    [Abstract] [Full Text] [Related]

  • 6. First case of ataxia with isolated vitamin E deficiency in the Netherlands.
    Ponten SC, Kwee ML, Wolters ECh, Zijlmans JC.
    Parkinsonism Relat Disord; 2007 Jul; 13(5):315-6. PubMed ID: 17049453
    [Abstract] [Full Text] [Related]

  • 7. Attempts to identify the chromosomal localization of the Friedreich's ataxia locus.
    Chamberlain S, Worrall C, Williamson R.
    Adv Neurol; 1988 Jul; 48():257-60. PubMed ID: 2891256
    [No Abstract] [Full Text] [Related]

  • 8. Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency.
    El Euch-Fayache G, Bouhlal Y, Amouri R, Feki M, Hentati F.
    Brain; 2014 Feb; 137(Pt 2):402-10. PubMed ID: 24369383
    [Abstract] [Full Text] [Related]

  • 9. Ataxia with vitamin E deficiency associated with deafness.
    Kara B, Uzümcü A, Uyguner O, Rosti RO, Koçbaş A, Ozmen M, Kayserili H.
    Turk J Pediatr; 2008 Feb; 50(5):471-5. PubMed ID: 19102053
    [Abstract] [Full Text] [Related]

  • 10. Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich's ataxia.
    Hammans SR, Kennedy CR.
    J Neurol Neurosurg Psychiatry; 1998 Mar; 64(3):368-70. PubMed ID: 9527151
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  • 19. Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia.
    Houshmand M, Panahi MS, Nafisi S, Soltanzadeh A, Alkandari FM.
    Mitochondrion; 2006 Apr; 6(2):82-8. PubMed ID: 16581313
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  • 20. Ataxia with vitamin E deficiency in southeast Norway, case report.
    Koht J, Bjørnarå KA, Jørum E, Tallaksen CM.
    Acta Neurol Scand Suppl; 2009 Apr; (189):42-5. PubMed ID: 19566498
    [Abstract] [Full Text] [Related]


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