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Journal Abstract Search

130 related items for PubMed ID: 7788963

  • 1. 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; 97(1):1-7. PubMed ID: 7788963
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  • 2. Ataxia telangiectasia.
    Paruthi SC, Singh H, Singh H.
    J Assoc Physicians India; 1991 Feb; 39(2):215-6. PubMed ID: 1885492
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  • 4. [Clinico-genetic diagnosis of ataxia telangiectatica (Louis-Bar syndrome)].
    Fuhrmann E, Pfeiffer L, Zschenderlein R, Leonhardt T, Melster U, Kölmel HW.
    Nervenarzt; 1993 Feb; 64(2):140-2. PubMed ID: 8450897
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  • 5. Ataxia-oculomotor apraxia syndrome.
    Gascon GG, Abdo N, Sigut D, Hemidan A, Hannan MA.
    J Child Neurol; 1995 Mar; 10(2):118-22. PubMed ID: 7782601
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  • 6. Choreas, hereditary and other ataxias, tics, myoclonus, and other movement disorders.
    Tolosa E, Berciano J.
    Curr Opin Neurol Neurosurg; 1993 Jun; 6(3):358-68. PubMed ID: 8507906
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  • 10. Amyotrophic lateral sclerosis: a possible example of autosomal recessive inheritance.
    Della Sala S, Lalatta F, Mazzini L.
    Schweiz Arch Neurol Psychiatr (1985); 1991 Jun; 142(2):139-47. PubMed ID: 1710388
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  • 16. Cerebral white-matter changes suggesting leukodystrophy in ataxia telangiectasia.
    Chung EO, Bodensteiner JB, Noorani PA, Schochet SS.
    J Child Neurol; 1994 Jan; 9(1):31-5. PubMed ID: 7512106
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  • 17. Familial paroxysmal ataxia: report of a family.
    Hawkes CH.
    J Neurol Neurosurg Psychiatry; 1992 Mar; 55(3):212-3. PubMed ID: 1564484
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  • 18. Consequences of the delayed diagnosis of ataxia-telangiectasia.
    Cabana MD, Crawford TO, Winkelstein JA, Christensen JR, Lederman HM.
    Pediatrics; 1998 Jul; 102(1 Pt 1):98-100. PubMed ID: 9651420
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