These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 38469975)

  • 1. Distinct neural signatures of pulvinar in C9orf72 amyotrophic lateral sclerosis mutation carriers and noncarriers.
    Nigri A; Stanziano M; Fedeli D; Manera U; Ferraro S; Medina Carrion JP; Palermo S; Lequio L; Denegri F; Agosta F; Spinelli EG; Filippi M; Grisoli M; Valentini MC; De Mattei F; Canosa A; Calvo A; Chiò A; Bruzzone MG; Moglia C
    Eur J Neurol; 2024 Jun; 31(6):e16266. PubMed ID: 38469975
    [TBL] [Abstract][Full Text] [Related]  

  • 2. C9orf72 ALS mutation carriers show extensive cortical and subcortical damage compared to matched wild-type ALS patients.
    Nigri A; Umberto M; Stanziano M; Ferraro S; Fedeli D; Medina Carrion JP; Palermo S; Lequio L; Denegri F; Agosta F; Filippi M; Valentini MC; Canosa A; Calvo A; Chiò A; Bruzzone MG; Moglia C
    Neuroimage Clin; 2023; 38():103400. PubMed ID: 37068310
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Longitudinal imaging in
    Floeter MK; Bageac D; Danielian LE; Braun LE; Traynor BJ; Kwan JY
    Neuroimage Clin; 2016; 12():1035-1043. PubMed ID: 27995069
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Network degeneration and dysfunction in presymptomatic
    Lee SE; Sias AC; Mandelli ML; Brown JA; Brown AB; Khazenzon AM; Vidovszky AA; Zanto TP; Karydas AM; Pribadi M; Dokuru D; Coppola G; Geschwind DH; Rademakers R; Gorno-Tempini ML; Rosen HJ; Miller BL; Seeley WW
    Neuroimage Clin; 2017; 14():286-297. PubMed ID: 28337409
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion.
    Lee SE; Khazenzon AM; Trujillo AJ; Guo CC; Yokoyama JS; Sha SJ; Takada LT; Karydas AM; Block NR; Coppola G; Pribadi M; Geschwind DH; Rademakers R; Fong JC; Weiner MW; Boxer AL; Kramer JH; Rosen HJ; Miller BL; Seeley WW
    Brain; 2014 Nov; 137(Pt 11):3047-60. PubMed ID: 25273996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deficits in verbal fluency in presymptomatic
    Lulé DE; Müller HP; Finsel J; Weydt P; Knehr A; Winroth I; Andersen P; Weishaupt J; Uttner I; Kassubek J; Ludolph AC
    J Neurol Neurosurg Psychiatry; 2020 Nov; 91(11):1195-1200. PubMed ID: 32855285
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thalamic nuclei in frontotemporal dementia: Mediodorsal nucleus involvement is universal but pulvinar atrophy is unique to C9orf72.
    Bocchetta M; Iglesias JE; Neason M; Cash DM; Warren JD; Rohrer JD
    Hum Brain Mapp; 2020 Mar; 41(4):1006-1016. PubMed ID: 31696638
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Differential Neuropsychological Profile of Patients With Amyotrophic Lateral Sclerosis With and Without
    Iazzolino B; Peotta L; Zucchetti JP; Canosa A; Manera U; Vasta R; Grassano M; Palumbo F; Brunetti M; Barberis M; Sbaiz L; Moglia C; Calvo A; Chiò A
    Neurology; 2021 Jan; 96(1):e141-e152. PubMed ID: 33106391
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The involvement of language-associated networks, tracts, and cortical regions in frontotemporal dementia and amyotrophic lateral sclerosis: Structural and functional alterations.
    Tahedl M; Tan EL; Chipika RH; Lope J; Hengeveld JC; Doherty MA; McLaughlin RL; Hardiman O; Hutchinson S; McKenna MC; Bede P
    Brain Behav; 2023 Nov; 13(11):e3250. PubMed ID: 37694825
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Presymptomatic grey matter alterations in ALS kindreds: a computational neuroimaging study of asymptomatic C9orf72 and SOD1 mutation carriers.
    Bede P; Lulé D; Müller HP; Tan EL; Dorst J; Ludolph AC; Kassubek J
    J Neurol; 2023 Sep; 270(9):4235-4247. PubMed ID: 37178170
    [TBL] [Abstract][Full Text] [Related]  

  • 11. "Switchboard" malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis.
    Chipika RH; Finegan E; Li Hi Shing S; McKenna MC; Christidi F; Chang KM; Doherty MA; Hengeveld JC; Vajda A; Pender N; Hutchinson S; Donaghy C; McLaughlin RL; Hardiman O; Bede P
    Neuroimage Clin; 2020; 27():102300. PubMed ID: 32554322
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The neural correlates and clinical characteristics of psychosis in the frontotemporal dementia continuum and the
    Devenney EM; Landin-Romero R; Irish M; Hornberger M; Mioshi E; Halliday GM; Kiernan MC; Hodges JR
    Neuroimage Clin; 2017; 13():439-445. PubMed ID: 28116236
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterogeneous brain FDG-PET metabolic patterns in patients with C9orf72 mutation.
    Castelnovo V; Caminiti SP; Riva N; Magnani G; Silani V; Perani D
    Neurol Sci; 2019 Mar; 40(3):515-521. PubMed ID: 30554355
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Radiogenomics of
    Bonham LW; Geier EG; Sirkis DW; Leong JK; Ramos EM; Wang Q; Karydas A; Lee SE; Sturm VE; Sawyer RP; Friedberg A; Ichida JK; Gitler AD; Sugrue L; Cordingley M; Bee W; Weber E; Kramer JH; Rankin KP; Rosen HJ; Boxer AL; Seeley WW; Ravits J; Miller BL; Yokoyama JS
    J Neurosci; 2023 Jan; 43(2):333-345. PubMed ID: 36446586
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile.
    Devenney E; Hornberger M; Irish M; Mioshi E; Burrell J; Tan R; Kiernan MC; Hodges JR
    JAMA Neurol; 2014 Mar; 71(3):331-9. PubMed ID: 24445580
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Connectivity-based characterisation of subcortical grey matter pathology in frontotemporal dementia and ALS: a multimodal neuroimaging study.
    Bede P; Omer T; Finegan E; Chipika RH; Iyer PM; Doherty MA; Vajda A; Pender N; McLaughlin RL; Hutchinson S; Hardiman O
    Brain Imaging Behav; 2018 Dec; 12(6):1696-1707. PubMed ID: 29423814
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p.
    Hsiung GY; DeJesus-Hernandez M; Feldman HH; Sengdy P; Bouchard-Kerr P; Dwosh E; Butler R; Leung B; Fok A; Rutherford NJ; Baker M; Rademakers R; Mackenzie IR
    Brain; 2012 Mar; 135(Pt 3):709-22. PubMed ID: 22344582
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Resting-state fMRI functional connectome of C9orf72 mutation status.
    Stanziano M; Fedeli D; Manera U; Ferraro S; Medina Carrion JP; Palermo S; Sciortino P; Cogoni M; Agosta F; Basaia S; Filippi M; Grisoli M; Valentini MC; De Mattei F; Canosa A; Calvo A; Bruzzone MG; Chiò A; Nigri A; Moglia C
    Ann Clin Transl Neurol; 2024 Mar; 11(3):686-697. PubMed ID: 38234062
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
    Van Mossevelde S; van der Zee J; Gijselinck I; Engelborghs S; Sieben A; Van Langenhove T; De Bleecker J; Baets J; Vandenbulcke M; Van Laere K; Ceyssens S; Van den Broeck M; Peeters K; Mattheijssens M; Cras P; Vandenberghe R; De Jonghe P; Martin JJ; De Deyn PP; Cruts M; Van Broeckhoven C;
    Brain; 2016 Feb; 139(Pt 2):452-67. PubMed ID: 26674655
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Eye movement alterations in presymptomatic C9orf72 expansion gene carriers.
    Behler A; Knehr A; Finsel J; Kunz MS; Lang C; Müller K; Müller HP; Pinkhardt EH; Ludolph AC; Lulé D; Kassubek J
    J Neurol; 2021 Sep; 268(9):3390-3399. PubMed ID: 33709219
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.