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Journal Abstract Search

122 related items for PubMed ID: 7307870

  • 1. Ophthalmoplegia-plus.
    Godel V, Nemet P, Reider-Groswasser I, Messer G, Lazar M.
    Doc Ophthalmol; 1981 Nov; 51(4):373-82. PubMed ID: 7307870
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  • 2. Kearns-Sayre syndrome.
    Nemet P, Godel V, Lazar M.
    Birth Defects Orig Artic Ser; 1982 Nov; 18(6):263-8. PubMed ID: 7171761
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  • 3. [Progressive external ophthalmoplegia and its associations. A case with ocular hypertension, tapeto-retinal degeneration and cardiac alterations].
    Bec P, Arne JL.
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 Dec; 34(12):879-86. PubMed ID: 4282463
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  • 5. Autosomal dominant Kearns-Sayre syndrome.
    Leveille AS, Newell FW.
    Ophthalmology; 1980 Feb; 87(2):99-108. PubMed ID: 7383548
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  • 6. [Kearns syndrome. Progressive external ophthalmoplegia, retinal pigment degeneration and heart conduction disorders].
    Boltshauser E, Jerusalem F, Niemeyer G, Huber C.
    Schweiz Med Wochenschr; 1977 Dec 17; 107(50):1880-8. PubMed ID: 594731
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  • 7. Jensen's rectus muscle union in paralytic esotropia.
    Chen QK, Zang Q.
    Chin Med J (Engl); 1980 Sep 17; 93(9):647-9. PubMed ID: 6775899
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  • 9. Third degree atrioventricular block, chronic progressive external ophthalmoplegia and pigmentary degeneration of retina. Case report and survey of the literature.
    Petersen E.
    Acta Med Scand; 1978 Sep 17; 203(1-2):39-42. PubMed ID: 626112
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  • 10. Special types of muscle anomalies associated with Graves' disease.
    Knapp P.
    Ophthalmology; 1979 Dec 17; 86(12):2081-4. PubMed ID: 583615
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  • 13. Acquired Adult Onset Cyclic Esotropia in Patients With Myopic Strabismus Fixus and Intraocular Lens Implantation.
    Yan J, Wen Y.
    J Craniofac Surg; 2017 Sep 17; 28(6):e513-e515. PubMed ID: 28692503
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  • 14. [Surgical treatment of paralytic convergent strabismus using a modification of Jensen's method].
    Krstić L, Drincić R, Smiljanić N, Milosavljević K.
    Vojnosanit Pregl; 1993 Sep 17; 50(3):262-5. PubMed ID: 8212652
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  • 17. A dominantly inherited progressive disease in a black family characterised by cerebellar and retinal degeneration, external ophthalmoplegia and abnormal mitochondria.
    Cooles P, Michaud R, Best PV.
    J Neurol Sci; 1988 Nov 17; 87(2-3):275-88. PubMed ID: 3210038
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