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

226 related items for PubMed ID: 11298681

  • 1. Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families.
    Marzouki N, Belal S, Benhamida C, Benlemlih M, Hentati F.
    Clin Genet; 2001 Apr; 59(4):257-62. PubMed ID: 11298681
    [Abstract] [Full Text] [Related]

  • 2. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci.
    Bouhlal Y, El-Euch-Fayeche G, Amouri R, Hentati F.
    Acta Myol; 2005 Oct; 24(2):155-61. PubMed ID: 16550933
    [Abstract] [Full Text] [Related]

  • 3. Primary degenerative cerebellar ataxias in ethnic Bengalees in West Bengal: some observations.
    Chakravarty A, Mukherjee SC.
    Neurol India; 2003 Jun; 51(2):227-34. PubMed ID: 14571010
    [Abstract] [Full Text] [Related]

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

  • 5. Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.
    Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F.
    Neurology; 2000 Apr 11; 54(7):1408-14. PubMed ID: 10751248
    [Abstract] [Full Text] [Related]

  • 6. Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
    Schöls L, Amoiridis G, Przuntek H, Frank G, Epplen JT, Epplen C.
    Brain; 1997 Dec 11; 120 ( Pt 12)():2131-40. PubMed ID: 9448568
    [Abstract] [Full Text] [Related]

  • 7. Sequence variation in GAA repeat expansions may cause differential phenotype display in Friedreich's ataxia.
    McDaniel DO, Keats B, Vedanarayanan VV, Subramony SH.
    Mov Disord; 2001 Nov 11; 16(6):1153-8. PubMed ID: 11748752
    [Abstract] [Full Text] [Related]

  • 8. Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.
    De Castro M, García-Planells J, Monrós E, Cañizares J, Vázquez-Manrique R, Vílchez JJ, Urtasun M, Lucas M, Navarro G, Izquierdo G, Moltó MD, Palau F.
    Hum Genet; 2000 Jan 11; 106(1):86-92. PubMed ID: 10982187
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Early onset cerebellar ataxia with retained tendon reflexes. Clinical, electrophysiological and MRI observations in comparison with Friedreich's ataxia.
    Klockgether T, Petersen D, Grodd W, Dichgans J.
    Brain; 1991 Aug 11; 114 ( Pt 4)():1559-73. PubMed ID: 1884166
    [Abstract] [Full Text] [Related]

  • 11. 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 11; 43(11):2179-83. PubMed ID: 8232925
    [Abstract] [Full Text] [Related]

  • 12. Autosomal recessive cerebellar ataxias.
    Palau F, Espinós C.
    Orphanet J Rare Dis; 2006 Nov 17; 1():47. PubMed ID: 17112370
    [Abstract] [Full Text] [Related]

  • 13. 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 Nov 17; 48(1):21-8. PubMed ID: 15953402
    [Abstract] [Full Text] [Related]

  • 14. Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.
    Bouhlal Y, Zouari M, Kefi M, Ben Hamida C, Hentati F, Amouri R.
    J Neurogenet; 2008 Nov 17; 22(2):139-48. PubMed ID: 18569450
    [Abstract] [Full Text] [Related]

  • 15. Very late onset Friedreich's ataxia without cardiomyopathy is associated with limited GAA expansion in the X25 gene.
    Gellera C, Pareyson D, Castellotti B, Mazzucchelli F, Zappacosta B, Pandolfo M, Di Donato S.
    Neurology; 1997 Oct 17; 49(4):1153-5. PubMed ID: 9339708
    [Abstract] [Full Text] [Related]

  • 16. Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
    Sridharan R, Radhakrishnan K, Ashok PP, Mousa ME.
    Brain; 1985 Dec 17; 108 ( Pt 4)():831-43. PubMed ID: 4075075
    [Abstract] [Full Text] [Related]

  • 17. Typical Friedreich's ataxia without GAA expansions and GAA expansion without typical Friedreich's ataxia.
    McCabe DJ, Ryan F, Moore DP, McQuaid S, King MD, Kelly A, Daly K, Barton DE, Murphy RP.
    J Neurol; 2000 May 17; 247(5):346-55. PubMed ID: 10896266
    [Abstract] [Full Text] [Related]

  • 18. Early onset cerebellar ataxia with retained tendon reflexes: foot deformity in a first grade family member.
    Schelhaas HJ, Hulst MV, Ippel E, Prevo RL, Hageman G.
    Clin Neurol Neurosurg; 1999 Dec 17; 101(4):253-5. PubMed ID: 10622455
    [Abstract] [Full Text] [Related]

  • 19. Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families.
    Benomar A, Yahyaoui M, Meggouh F, Bouhouche A, Boutchich M, Bouslam N, Zaim A, Schmitt M, Belaidi H, Ouazzani R, Chkili T, Koenig M.
    J Neurol Sci; 2002 Jun 15; 198(1-2):25-9. PubMed ID: 12039660
    [Abstract] [Full Text] [Related]

  • 20. Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.
    Belal S, Hentati F, Ben Hamida C, Ben Hamida M.
    Clin Neurosci; 1995 Jun 15; 3(1):39-42. PubMed ID: 7614093
    [Abstract] [Full Text] [Related]

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