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PUBMED FOR HANDHELDS

Journal Abstract Search


214 related items for PubMed ID: 19005991

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  • 6. [Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family].
    Sakka R, Kerkeni E, Chaabouni M, Chioukh FZ, Ben Amor S, M'rad R, Ben Yahia S, Chaabouni H, Monastiri K.
    Tunis Med; 2015 Mar; 93(3):170-4. PubMed ID: 26367406
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  • 7. Retinal detachment and prophylaxis in type 1 Stickler syndrome.
    Ang A, Poulson AV, Goodburn SF, Richards AJ, Scott JD, Snead MP.
    Ophthalmology; 2008 Jan; 115(1):164-8. PubMed ID: 17675240
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  • 8. Distinguishing Marshall from Stickler syndrome: a clinical and genetic challenge.
    Janssen EJM, Stegmann APA, Stumpel CTRM.
    Clin Dysmorphol; 2021 Jan; 30(1):58-61. PubMed ID: 32897902
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  • 12. Hunter syndrome (MPS II-B): a report of bilateral vitreous floaters and maculopathy.
    Anawis MA.
    Ophthalmic Genet; 2006 Jun; 27(2):71-2. PubMed ID: 16754210
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  • 13. [Vitreous changes in Stickler syndrome].
    Betis F, Hofman P, Gastaud P.
    J Fr Ophtalmol; 2003 Apr; 26(4):386-90. PubMed ID: 12843897
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  • 15. Hereditary vitreoretinal degeneration, cleft lip and palate, deafness, and skeletal dysplasia.
    Regenbogen L, Godel V.
    Am J Ophthalmol; 1980 Mar; 89(3):414-8. PubMed ID: 6966133
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  • 16. [Two cases of Kniest dysplasia--ocular manifestations].
    Kagotani Y, Takao K, Nomura K, Okubo K.
    Nippon Ganka Gakkai Zasshi; 1995 Mar; 99(3):376-83. PubMed ID: 7732932
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  • 18. Clinical features of the congenital vitreoretinopathies.
    Edwards AO.
    Eye (Lond); 2008 Oct; 22(10):1233-42. PubMed ID: 18309337
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