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

68 related items for PubMed ID: 5860349

  • 1. [On a rare familial association of the Brown syndrome with the Marcus Gunn phenomenon].
    Artifoni E, Bertoncini G.
    Ann Ottalmol Clin Ocul; 1965 Jul; 91(7):563-76. PubMed ID: 5860349
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles.
    Brodsky MC.
    Ophthalmology; 1998 Apr; 105(4):717-25. PubMed ID: 9544647
    [Abstract] [Full Text] [Related]

  • 3. The Marcus Gunn phenomenon: discussion and report of three cases.
    Chattopadhyay A, Srinivas K, Sharatchandra B, Kannan N.
    Quintessence Int; 1995 Aug; 26(8):563-6. PubMed ID: 8602433
    [Abstract] [Full Text] [Related]

  • 4. [THE MARCUS-GUNN PHENOMENON ASSOCIATED WITH OCULOMOTOR PARALYSIS AND PERSISTENCE OF THE HYALOID VESSELS].
    CIURLO G.
    Minerva Oftalmol; 1965 Aug; 7(2):65-7. PubMed ID: 14343602
    [No Abstract] [Full Text] [Related]

  • 5. [On the problem of the surgical treatment of the Marcus Gunn synkinetic syndrome in children].
    Virnik LG.
    Vestn Oftalmol; 1967 Aug; 80(4):33-5. PubMed ID: 5609245
    [No Abstract] [Full Text] [Related]

  • 6. [Congenital disorders of the oculomotor system among our cases. Brown's syndrome and Marcus-Gunn synkinesis].
    Krzystkowa KM, Kubatko-Zielińska A.
    Klin Oczna; 1984 Sep; 86(9):383-5. PubMed ID: 6530882
    [No Abstract] [Full Text] [Related]

  • 7. Oculogastrointestinal muscular dystrophy.
    Ionasescu V.
    Am J Med Genet; 1983 May; 15(1):103-12. PubMed ID: 6859110
    [Abstract] [Full Text] [Related]

  • 8. Inverse Marcus Gunn phenomenon.
    Prakash MV, Radhakrishnan M, Yogeshwari A, Nazir W, Maragatham K, Natarajan K.
    Indian J Ophthalmol; 2002 Jun; 50(2):142-4. PubMed ID: 12194575
    [Abstract] [Full Text] [Related]

  • 9. [3 cases of familial external partial bulbar ophthalmoplegia of the "crawfish eye" type].
    Rubino A, Scialfa A.
    Riv Otoneurooftalmol; 1968 Jun; 43(1):1-16. PubMed ID: 5704991
    [No Abstract] [Full Text] [Related]

  • 10. [The Marcus Gunn phenomenon].
    Raverdy P, Theron HP, Souillard C, Remy A.
    Rev Neurol (Paris); 1984 Jun; 140(12):734-7. PubMed ID: 6522914
    [Abstract] [Full Text] [Related]

  • 11. [On paradoxical movement of the upper eyelids (Marcus Gunn syndrome)].
    Koshel' AI.
    Vestn Oftalmol; 1967 Jun; 80(4):79-80. PubMed ID: 5609256
    [No Abstract] [Full Text] [Related]

  • 12. [A case of Marcus-Gunn phenomenon with oculomotor paralysis].
    Kaluzny J.
    Klin Oczna; 1967 Jun; 37(3):389-93. PubMed ID: 5602749
    [No Abstract] [Full Text] [Related]

  • 13. Familial Richner-Hanhart syndrome: genetic, clinical, and metabolic studies.
    Sammartino A, de Crecchio G, Balato N, Lembo G, Federico A, Pallini R.
    Ann Ophthalmol; 1984 Nov; 16(11):1069-74. PubMed ID: 6240214
    [Abstract] [Full Text] [Related]

  • 14. [Congenital familial external ophthalmoplegia].
    Koraszewska-Matuszewska B, Samochowiec-Donocikowa E.
    Klin Oczna; 1984 Oct; 86(10):427-8. PubMed ID: 6535872
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. [Range of variation of clinical forms of congenital familial motility disorders].
    Roggenkämper P, Mertz M.
    Fortschr Ophthalmol; 1984 Oct; 81(4):385-7. PubMed ID: 6479811
    [No Abstract] [Full Text] [Related]

  • 19. [Marcus-Gunn Syndrome. Based on a case report].
    Tahri H, Benatiya I, Bhalil S, Masbahi I, Bouayad A, Daoudi K, Touiza L.
    Bull Soc Belge Ophtalmol; 2004 Oct; (294):45-8. PubMed ID: 15682918
    [Abstract] [Full Text] [Related]

  • 20. [Familial juvenile nephronophthisis].
    Breker H, Hanrath R, Severin M, Finke K, Renner E.
    Med Welt; 1973 Oct 05; 24(40):1518-20. PubMed ID: 4764049
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.