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Journal Abstract Search

177 related items for PubMed ID: 18479928

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  • 23. Serum progranulin levels in patients with frontotemporal lobar degeneration and Alzheimer's disease: detection of GRN mutations in a Spanish cohort.
    Antonell A, Gil S, Sánchez-Valle R, Balasa M, Bosch B, Prat MC, Chiollaz AC, Fernández M, Yagüe J, Molinuevo JL, Lladó A.
    J Alzheimers Dis; 2012; 31(3):581-91. PubMed ID: 22647257
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  • 26. Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.
    López de Munain A, Alzualde A, Gorostidi A, Otaegui D, Ruiz-Martínez J, Indakoetxea B, Ferrer I, Pérez-Tur J, Sáenz A, Bergareche A, Barandiarán M, Poza JJ, Zabalza R, Ruiz I, Urtasun M, Fernández-Manchola I, Olasagasti B, Espinal JB, Olaskoaga J, Ruibal M, Moreno F, Carrera N, Martí Massó JF.
    Biol Psychiatry; 2008 May 15; 63(10):946-52. PubMed ID: 17950702
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  • 27. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
    Gass J, Cannon A, Mackenzie IR, Boeve B, Baker M, Adamson J, Crook R, Melquist S, Kuntz K, Petersen R, Josephs K, Pickering-Brown SM, Graff-Radford N, Uitti R, Dickson D, Wszolek Z, Gonzalez J, Beach TG, Bigio E, Johnson N, Weintraub S, Mesulam M, White CL, Woodruff B, Caselli R, Hsiung GY, Feldman H, Knopman D, Hutton M, Rademakers R.
    Hum Mol Genet; 2006 Oct 15; 15(20):2988-3001. PubMed ID: 16950801
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  • 28. Alteration in cell cycle-related proteins in lymphoblasts from carriers of the c.709-1G>A PGRN mutation associated with FTLD-TDP dementia.
    Alquezar C, Esteras N, Bartolomé F, Merino JJ, Alzualde A, López de Munain A, Martín-Requero Á.
    Neurobiol Aging; 2012 Feb 15; 33(2):429.e7-20. PubMed ID: 21232819
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  • 30. Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.
    Whitwell JL, Jack CR, Baker M, Rademakers R, Adamson J, Boeve BF, Knopman DS, Parisi JF, Petersen RC, Dickson DW, Hutton ML, Josephs KA.
    Arch Neurol; 2007 Mar 15; 64(3):371-6. PubMed ID: 17353379
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  • 36. The granulin gene family: from cancer to dementia.
    Bateman A, Bennett HP.
    Bioessays; 2009 Nov 15; 31(11):1245-54. PubMed ID: 19795409
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  • 37. Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.
    Skoglund L, Brundin R, Olofsson T, Kalimo H, Ingvast S, Blom ES, Giedraitis V, Ingelsson M, Lannfelt L, Basun H, Glaser A.
    Neurogenetics; 2009 Feb 15; 10(1):27-34. PubMed ID: 18855025
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  • 38. Clinicopathologic correlation in PGRN mutations.
    Davion S, Johnson N, Weintraub S, Mesulam MM, Engberg A, Mishra M, Baker M, Adamson J, Hutton M, Rademakers R, Bigio EH.
    Neurology; 2007 Sep 11; 69(11):1113-21. PubMed ID: 17522386
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  • 39. Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series.
    Borroni B, Archetti S, Alberici A, Agosti C, Gennarelli M, Bigni B, Bonvicini C, Ferrari M, Bellelli G, Galimberti D, Scarpini E, Di Lorenzo D, Caimi L, Caltagirone C, Di Luca M, Padovani A.
    Neurogenetics; 2008 Jul 11; 9(3):197-205. PubMed ID: 18392865
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  • 40. Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration.
    Krüger J, Kaivorinne AL, Udd B, Majamaa K, Remes AM.
    Eur J Neurol; 2009 Jan 11; 16(1):27-30. PubMed ID: 19049508
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