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Journal Abstract Search

326 related items for PubMed ID: 17441379

  • 1. [Ocular findings in patients with Steinert myotonic dystrophy].
    Markowska E, Zalewska R, Mariak Z, Wojnar M.
    Przegl Lek; 2006; 63(8):662-3. PubMed ID: 17441379
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  • 2. [Retinopathy of myotonic dystrophy (Steinert)].
    Remky H.
    Bull Mem Soc Fr Ophtalmol; 1972; 85(0):500-4. PubMed ID: 4671825
    [No Abstract] [Full Text] [Related]

  • 3. [Myotonic retinopathy].
    Remky H.
    Klin Monbl Augenheilkd; 1972 Oct; 161(4):372-87. PubMed ID: 4539596
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  • 4. [Maculopathy in Curschmann-Steinert myotonic dystrophy].
    Giusti C.
    Recenti Prog Med; 2003 Jan; 94(1):16-8. PubMed ID: 12632995
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  • 5. [Reticular macular dystrophy and Steinert disease].
    Dumont P, Malthieu D, Turut P, Milazzo S, Sellam R.
    Bull Soc Ophtalmol Fr; 1989 Feb; 89(2):277-8, 281-2. PubMed ID: 2805202
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  • 6. [Maculopathy in Curschmann-Steinert myotonic dystrophy].
    Austermann P, Kuba GB, Kroll P.
    Ophthalmologe; 2000 Nov; 97(11):784-7. PubMed ID: 11130169
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  • 9. [Ocular hypotonia and retinal injuries in Steinert disease. Angiographic aspects].
    Raby O, Bonsch M.
    J Fr Ophtalmol; 1986 Nov; 9(8-9):543-52. PubMed ID: 3819327
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  • 10. Coincident trinucleotide repeat expansions in a patient with myotonic dystrophy type 1 and spinocerebellar ataxia.
    Kolb SJ, Kissel JT.
    J Clin Neuromuscul Dis; 2008 Sep; 10(1):22-3. PubMed ID: 18772697
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  • 12. The expanding clinical and genetic spectrum of the myotonic dystrophies.
    Ricker K.
    Acta Neurol Belg; 2000 Sep; 100(3):151-5. PubMed ID: 11098287
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  • 19. Intergenerational changes of CTG repeat depending on the sex of the transmitting parent in myotonic dystrophy type 1.
    Rakocević-Stojanović V, Savić D, Pavlović S, Lavrnić D, Stević Z, Basta I, Romac S, Apostolski S.
    Eur J Neurol; 2005 Mar; 12(3):236-7. PubMed ID: 15693817
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  • 20. [Multiorgan manifestations in myotonic dystrophy type 1].
    Varga D, Pál E.
    Orv Hetil; 2019 Sep; 160(37):1447-1454. PubMed ID: 31495190
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