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Journal Abstract Search

374 related items for PubMed ID: 28462717

  • 21. Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort.
    Samra K, MacDougall AM, Bouzigues A, Bocchetta M, Cash DM, Greaves CV, Convery RS, van Swieten JC, Jiskoot L, Seelaar H, Moreno F, Sanchez-Valle R, Laforce R, Graff C, Masellis M, Tartaglia MC, Rowe JB, Borroni B, Finger E, Synofzik M, Galimberti D, Vandenberghe R, de Mendonça A, Butler CR, Gerhard A, Ducharme S, Le Ber I, Tiraboschi P, Santana I, Pasquier F, Levin J, Otto M, Sorbi S, Rohrer JD, Russell LL, Genetic FTD Initiative (GENFI).
    J Neurol Sci; 2023 Aug 15; 451():120711. PubMed ID: 37348248
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  • 22. Sex differences in the prevalence of genetic mutations in FTD and ALS: A meta-analysis.
    Curtis AF, Masellis M, Hsiung GR, Moineddin R, Zhang K, Au B, Millett G, Mackenzie I, Rogaeva E, Tierney MC.
    Neurology; 2017 Oct 10; 89(15):1633-1642. PubMed ID: 28916533
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  • 26. Long Non-Coding RNA Profile in Genetic Symptomatic and Presymptomatic Frontotemporal Dementia: A GENFI Study.
    Serpente M, Fenoglio C, Arcaro M, Carandini T, Sacchi L, Pintus M, Rotondo E, Borracci V, Ghezzi L, Bouzigues A, Russell LL, Foster PH, Ferry-Bolder E, van Swieten JC, Jiskoot LC, Seelaar H, Sánchez Valle R, Laforce R, Graff C, Vandenberghe R, de Mendonça A, Tiraboschi P, Santana I, Gerhard A, Levin J, Sorbi S, Otto M, Pasquier F, Ducharme S, Butler CR, Le Ber I, Finger E, Tartaglia MC, Masellis M, Rowe JB, Synofzik M, Moreno F, Borroni B, Rohrer JD, Arighi A, Galimberti D, Genetic FTD Initiative GENFI .
    J Alzheimers Dis; 2024 Oct 10; 100(s1):S187-S196. PubMed ID: 39121124
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  • 27. A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort.
    Moore K, Convery R, Bocchetta M, Neason M, Cash DM, Greaves C, Russell LL, Clarke MTM, Peakman G, van Swieten J, Jiskoot L, Moreno F, Barandiaran M, Sanchez-Valle R, Borroni B, Laforce R, Doré MC, Masellis M, Tartaglia MC, Graff C, Galimberti D, Rowe JB, Finger E, Synofzik M, Karnath HO, Vandenberghe R, de Mendonça A, Maruta C, Tagliavini F, Santana I, Ducharme S, Butler C, Gerhard A, Levin J, Danek A, Otto M, Warren JD, Rohrer JD, Genetic FTD Initiative, GENFI*.
    Appl Neuropsychol Adult; 2022 Oct 10; 29(1):112-119. PubMed ID: 32024404
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  • 28. Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia.
    Sogorb-Esteve A, Nilsson J, Swift IJ, Heller C, Bocchetta M, Russell LL, Peakman G, Convery RS, van Swieten JC, Seelaar H, Borroni B, Galimberti D, Sanchez-Valle R, Laforce R, Moreno F, Synofzik M, Graff C, Masellis M, Tartaglia MC, Rowe JB, Vandenberghe R, Finger E, Tagliavini F, Santana I, Butler CR, Ducharme S, Gerhard A, Danek A, Levin J, Otto M, Sorbi S, Le Ber I, Pasquier F, Gobom J, Brinkmalm A, Blennow K, Zetterberg H, Rohrer JD, GENetic FTD Initiative.
    Alzheimers Res Ther; 2022 Aug 31; 14(1):118. PubMed ID: 36045450
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  • 30. Frontotemporal dementia.
    Deleon J, Miller BL.
    Handb Clin Neurol; 2018 Aug 31; 148():409-430. PubMed ID: 29478591
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  • 31. Distinct Neuroanatomical Correlates of Neuropsychiatric Symptoms in the Three Main Forms of Genetic Frontotemporal Dementia in the GENFI Cohort.
    Sellami L, Bocchetta M, Masellis M, Cash DM, Dick KM, van Swieten J, Borroni B, Galimberti D, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni G, Finger E, de Mendonça A, Sorbi S, Warren JD, Rohrer JD, Laforce R, Genetic FTD Initiative, GENFI.
    J Alzheimers Dis; 2018 Aug 31; 65(1):147-163. PubMed ID: 30010122
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  • 32. Cerebral blood flow in presymptomatic MAPT and GRN mutation carriers: A longitudinal arterial spin labeling study.
    Dopper EG, Chalos V, Ghariq E, den Heijer T, Hafkemeijer A, Jiskoot LC, de Koning I, Seelaar H, van Minkelen R, van Osch MJ, Rombouts SA, van Swieten JC.
    Neuroimage Clin; 2016 Aug 31; 12():460-5. PubMed ID: 27625986
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  • 33. Confirmation of high frequency of C9orf72 mutations in patients with frontotemporal dementia from Sweden.
    Öijerstedt L, Chiang HH, Björkström J, Forsell C, Lilius L, Lindström AK, Thonberg H, Graff C.
    Neurobiol Aging; 2019 Dec 31; 84():241.e21-241.e25. PubMed ID: 30992141
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  • 34. Patterns of regional cerebellar atrophy in genetic frontotemporal dementia.
    Bocchetta M, Cardoso MJ, Cash DM, Ourselin S, Warren JD, Rohrer JD.
    Neuroimage Clin; 2016 Dec 31; 11():287-290. PubMed ID: 26977398
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  • 35. A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy.
    Sassi C, Capozzo R, Gibbs R, Crews C, Zecca C, Arcuti S, Copetti M, Barulli MR, Brescia V, Singleton AB, Logroscino G.
    J Alzheimers Dis; 2016 May 30; 53(2):475-85. PubMed ID: 27258413
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  • 36. The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects.
    Blauwendraat C, Wilke C, Simón-Sánchez J, Jansen IE, Reifschneider A, Capell A, Haass C, Castillo-Lizardo M, Biskup S, Maetzler W, Rizzu P, Heutink P, Synofzik M.
    Genet Med; 2018 Feb 30; 20(2):240-249. PubMed ID: 28749476
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  • 37. Circulating Non-Coding RNA Levels Are Altered in Autosomal Dominant Frontotemporal Dementia.
    Fenoglio C, Serpente M, Visconte C, Arcaro M, Sorrentino F, D'Anca M, Arighi A, Rotondo E, Vimercati R, Rossi G, Scarpini E, Galimberti D.
    Int J Mol Sci; 2022 Nov 25; 23(23):. PubMed ID: 36499048
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  • 38. Early symptoms in symptomatic and preclinical genetic frontotemporal lobar degeneration.
    Tavares TP, Mitchell DGV, Coleman KK, Coleman BL, Shoesmith CL, Butler CR, Santana I, Danek A, Gerhard A, de Mendonca A, Borroni B, Tartaglia MC, Graff C, Galimberti D, Tagliavini F, Moreno F, Frisoni G, Rowe JB, Levin J, Van Swieten JC, Otto M, Synofzik M, Sanchez-Valle R, Vandenberghe R, Laforce RJ, Ghidoni R, Sorbi S, Ducharme S, Masellis M, Rohrer J, Finger E, GENFI Initiative.
    J Neurol Neurosurg Psychiatry; 2020 Sep 25; 91(9):975-984. PubMed ID: 32769115
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  • 39. An update on genetic frontotemporal dementia.
    Greaves CV, Rohrer JD.
    J Neurol; 2019 Aug 25; 266(8):2075-2086. PubMed ID: 31119452
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  • 40. C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort.
    Tan YJ, Yong ACW, Foo JN, Lian MM, Lim WK, Dominguez J, Fong ZH, Narasimhalu K, Chiew HJ, Ng KP, Ting SKS, Kandiah N, Ng ASL.
    Ann Clin Transl Neurol; 2023 Apr 25; 10(4):568-578. PubMed ID: 36799407
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