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Journal Abstract Search
198 related items for PubMed ID: 25034270
1. Leukoencephalopathy, cerebral calcifications and cysts: a family study. Karlinger K, Tárnoki ÁD, Tárnoki DL, Polvi A, Lehesjoki AE, Kelemen A, Szegedi L, Turányi E, Kamondi A, Szűcs A. J Neurol; 2014 Oct; 261(10):1911-6. PubMed ID: 25034270 [Abstract] [Full Text] [Related]
2. 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 [No Abstract] [Full Text] [Related]
3. Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. Netravathi M, Kumari R, Kapoor S, Dakle P, Dwivedi MK, Roy SD, Pandey P, Saini J, Ramakrishna A, Navalli D, Satishchandra P, Pal PK, Kumar A, Faruq M. BMC Med Genet; 2015 Feb 10; 16():5. PubMed ID: 25928698 [Abstract] [Full Text] [Related]
5. 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 10; 171(5):445-9. PubMed ID: 25843205 [Abstract] [Full Text] [Related]
6. 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 May 10; 35(4):396-7. PubMed ID: 23635489 [No Abstract] [Full Text] [Related]
8. Cerebroretinal microangiopathy with calcifications and cysts: A case report. Xu W, Zhao J, Zhu Y, Zhang W. Medicine (Baltimore); 2017 Jan 10; 96(1):e5545. PubMed ID: 28072696 [Abstract] [Full Text] [Related]
10. 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 10; 41(4):363-367. PubMed ID: 32543263 [Abstract] [Full Text] [Related]