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232 related items for PubMed ID: 12717671
1. [Nasu Hakola disease: a report of the first two cases in Bolivia]. Molina-Monasterios MC, Molina-Abecia H. Rev Neurol; ; 36(9):837-40. PubMed ID: 12717671 [Abstract] [Full Text] [Related]
2. A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola disease. Kuroda R, Satoh J, Yamamura T, Anezaki T, Terada T, Yamazaki K, Obi T, Mizoguchi K. J Neurol Sci; 2007 Jan 15; 252(1):88-91. PubMed ID: 17125796 [Abstract] [Full Text] [Related]
6. Psychosocial reactions in the spouses of patients suffering polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy. Hakola HP. J Clin Psychiatry; 1990 Jan 15; 51(1):21-4. PubMed ID: 2295586 [Abstract] [Full Text] [Related]
7. Immunohistochemical characterization of microglia in Nasu-Hakola disease brains. Satoh J, Tabunoki H, Ishida T, Yagishita S, Jinnai K, Futamura N, Kobayashi M, Toyoshima I, Yoshioka T, Enomoto K, Arai N, Arima K. Neuropathology; 2011 Aug 15; 31(4):363-75. PubMed ID: 21118401 [Abstract] [Full Text] [Related]
8. Nasu-Hakola disease: The first case reported by Nasu and review: The 50th Anniversary of Japanese Society of Neuropathology. Kaneko M, Sano K, Nakayama J, Amano N. Neuropathology; 2010 Oct 15; 30(5):463-70. PubMed ID: 20500450 [Abstract] [Full Text] [Related]
10. Brain and bone damage in KARAP/DAP12 loss-of-function mice correlate with alterations in microglia and osteoclast lineages. Nataf S, Anginot A, Vuaillat C, Malaval L, Fodil N, Chereul E, Langlois JB, Dumontel C, Cavillon G, Confavreux C, Mazzorana M, Vico L, Belin MF, Vivier E, Tomasello E, Jurdic P. Am J Pathol; 2005 Jan 15; 166(1):275-86. PubMed ID: 15632019 [Abstract] [Full Text] [Related]
17. [Molecular Pathogenesis of Nasu-Hakola Disease Brain Lesions]. Satoh J. Brain Nerve; 2016 May 15; 68(5):543-50. PubMed ID: 27156507 [Abstract] [Full Text] [Related]
18. Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts. Paloneva J, Kestilä M, Wu J, Salminen A, Böhling T, Ruotsalainen V, Hakola P, Bakker AB, Phillips JH, Pekkarinen P, Lanier LL, Timonen T, Peltonen L. Nat Genet; 2000 Jul 15; 25(3):357-61. PubMed ID: 10888890 [Abstract] [Full Text] [Related]