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Journal Abstract Search

473 related items for PubMed ID: 25024321

  • 21. Secretory leukocyte protease inhibitor protein regulates the penetrance of frontotemporal lobar degeneration in progranulin mutation carriers.
    Ghidoni R, Flocco R, Paterlini A, Glionna M, Caruana L, Tonoli E, Binetti G, Benussi L.
    J Alzheimers Dis; 2014; 38(3):533-9. PubMed ID: 24018267
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  • 26. Progranulin transcripts with short and long 5' untranslated regions (UTRs) are differentially expressed via posttranscriptional and translational repression.
    Capell A, Fellerer K, Haass C.
    J Biol Chem; 2014 Sep 12; 289(37):25879-89. PubMed ID: 25056957
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  • 33. Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulin.
    Caroppo P, Le Ber I, Camuzat A, Clot F, Naccache L, Lamari F, De Septenville A, Bertrand A, Belliard S, Hannequin D, Colliot O, Brice A.
    JAMA Neurol; 2014 Dec 12; 71(12):1562-6. PubMed ID: 25317628
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  • 34. Clinical, neuropathological, and genetic characteristics of the novel IVS9+1delG GRN mutation in a patient with frontotemporal dementia.
    Taipa R, Tuna A, Damásio J, Pinto PS, Cavaco S, Pereira S, Milterberger-Miltenyi G, Galimberti D, Melo-Pires M.
    J Alzheimers Dis; 2012 Dec 12; 30(1):83-90. PubMed ID: 22366770
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  • 35. The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementia.
    Calvi A, Cioffi SM, Caffarra P, Fenoglio C, Serpente M, Pietroboni AM, Arighi A, Ghezzi L, Gardini S, Scarpini E, Galimberti D.
    J Alzheimers Dis; 2015 Dec 12; 44(1):277-82. PubMed ID: 25261445
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  • 37. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.
    Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, Rossor MN, Collinge J, Mead S.
    Brain; 2008 Mar 12; 131(Pt 3):706-20. PubMed ID: 18234697
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