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PUBMED FOR HANDHELDS

Journal Abstract Search


161 related items for PubMed ID: 22834668

  • 1. Progressive cerebroretinal microangiopathy with calcifications and cysts syndrome: an unusual cause of complex partial seizure.
    Dusak A, Seferoğlu M, Hakyemez B, Bora I, Parlak M.
    Psychiatry Clin Neurosci; 2012 Aug; 66(5):460. PubMed ID: 22834668
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  • 3. Retinopathy and bone marrow failure revealing Coats plus syndrome.
    Painho T, Conceição C, Kjöllerström P, Batalha S.
    BMJ Case Rep; 2018 Mar 09; 2018():. PubMed ID: 29523622
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  • 4. A case of late-onset leukoencephalopathy, calcifications, and cysts presenting with intracerebral hemorrhage resembling a neoplasm.
    Banks GP, Weiss SA, Pisapia D, Willey JZ.
    Cerebrovasc Dis; 2013 Mar 09; 35(4):396-7. PubMed ID: 23635489
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  • 6. [Neuroimaging findings in cerebroretinal microangiopathy with calcifications and cysts].
    Herrera DA, Vargas SA, Montoya C.
    Biomedica; 2014 Mar 09; 34(2):166-70. PubMed ID: 24967922
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  • 13. Leukoencephalopathy, cerebral calcifications, and cysts: case report.
    Osman NI, Lorincz MT, Hulsing KL, Gebarski SS.
    Clin Neurol Neurosurg; 2012 Jul 09; 114(6):806-9. PubMed ID: 22306422
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  • 14. A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations.
    Han E, Patel NA, Yannuzzi NA, Laura DM, Fan KC, Negron CI, Prakhunhungsit S, Thorson WL, Berrocal AM.
    Ophthalmic Genet; 2020 Aug 09; 41(4):363-367. PubMed ID: 32543263
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  • 15. Coats plus syndrome (cerebroretinal microangiopathy with calcifications and cysts-1): A case report.
    Morgado F, Batista M, Moreno A, Coutinho I.
    Pediatr Dermatol; 2021 Jan 09; 38(1):191-193. PubMed ID: 33010065
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  • 16. Unilateral Coats'-like disease and an intragenic deletion in the TERC gene: A case report.
    Peene G, Smets E, Legius E, Cassiman C.
    Ophthalmic Genet; 2018 Apr 09; 39(2):247-250. PubMed ID: 29161159
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  • 17. Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature review.
    Osman O, Labrune P, Reiner P, Sarov M, Nasser G, Riant F, Tournier-Lasserve E, Chabriat H, Denier C.
    Rev Neurol (Paris); 2020 Mar 09; 176(3):170-179. PubMed ID: 31521395
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  • 18. Gastrointestinal Hemorrhage: A Manifestation of the Telomere Biology Disorders.
    Himes RW, Chiou EH, Queliza K, Shouval DS, Somech R, Agarwal S, Jajoo K, Ziegler DS, Kratz CP, Huang J, Lucas TL, Myers KC, Nelson AS, DiNardo CD, Alter BP, Giri N, Khincha PP, McReynolds LJ, Dufour C, Pierri F, Goldman FD, Sherif Y, Savage SA, Miloh T, Bertuch AA.
    J Pediatr; 2021 Mar 09; 230():55-61.e4. PubMed ID: 32971146
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  • 20. Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene.
    Bisserbe A, Tertian G, Buffet C, Turhan A, Lambotte O, Nasser G, Alvin P, Tardieu M, Riant F, Bergametti F, Tournier-Lasserve E, Denier C.
    Rev Neurol (Paris); 2015 May 09; 171(5):445-9. PubMed ID: 25843205
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