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 *

115 related articles for article (PubMed ID: 31837909)

  • 1. One novel GRN null mutation, two different aphasia phenotypes.
    Coppola C; Oliva M; Saracino D; Pappatà S; Zampella E; Cimini S; Ricci M; Giaccone G; Di Iorio G; Rossi G
    Neurobiol Aging; 2020 Mar; 87():141.e9-141.e14. PubMed ID: 31837909
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation.
    Bessi V; Piaceri I; Padiglioni S; Bagnoli S; Berti V; Sorbi S; Nacmias B
    J Neurol Sci; 2018 Sep; 392():34-37. PubMed ID: 30097151
    [No Abstract]   [Full Text] [Related]  

  • 3. A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review.
    Hosaka T; Ishii K; Miura T; Mezaki N; Kasuga K; Ikeuchi T; Tamaoka A
    BMC Neurol; 2017 Sep; 17(1):182. PubMed ID: 28915852
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Primary Progressive Aphasia Associated With
    Saracino D; Ferrieux S; Noguès-Lassiaille M; Houot M; Funkiewiez A; Sellami L; Deramecourt V; Pasquier F; Couratier P; Pariente J; Géraudie A; Epelbaum S; Wallon D; Hannequin D; Martinaud O; Clot F; Camuzat A; Bottani S; Rinaldi D; Auriacombe S; Sarazin M; Didic M; Boutoleau-Bretonnière C; Thauvin-Robinet C; Lagarde J; Roué-Jagot C; Sellal F; Gabelle A; Etcharry-Bouyx F; Morin A; Coppola C; Levy R; Dubois B; Brice A; Colliot O; Gorno-Tempini ML; Teichmann M; Migliaccio R; Le Ber I;
    Neurology; 2021 Jul; 97(1):e88-e102. PubMed ID: 33980708
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms.
    Puoti G; Lerza MC; Ferretti MG; Bugiani O; Tagliavini F; Rossi G
    J Alzheimers Dis; 2014; 42(3):939-47. PubMed ID: 25024321
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Crossed aphasia confirmed by fMRI in a case with nonfluent variant of primary progressive aphasia carrying a GRN mutation.
    Canu E; Bessi V; Leocadi M; Padiglioni S; Nacmias B; Sorbi S; Filippi M; Agosta F
    J Neurol; 2019 May; 266(5):1274-1279. PubMed ID: 30923936
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Progranulin-associated PiB-negative logopenic primary progressive aphasia.
    Josephs KA; Duffy JR; Strand EA; Machulda MM; Vemuri P; Senjem ML; Perkerson RB; Baker MC; Lowe V; Jack CR; Rademakers R; Whitwell JL
    J Neurol; 2014 Mar; 261(3):604-14. PubMed ID: 24449064
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.
    Cioffi SM; Galimberti D; Barocco F; Spallazzi M; Fenoglio C; Serpente M; Arcaro M; Gardini S; Scarpini E; Caffarra P
    J Alzheimers Dis; 2016 Sep; 54(2):717-21. PubMed ID: 27567822
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal Dominant Frontotemporal Lobar Degeneration in a Filipino Family with Progranulin Mutation.
    Dominguez J; Ng A; Yu J; Guevarra AC; Daroy ML; Alfon A; Catindig JA; Dizon M; Santiago J; Del Moral MC; Yu J; Jamerlan A; Ligsay A; Bagyinszky E; An SS; Kim S
    Dement Geriatr Cogn Disord; 2020; 49(6):557-564. PubMed ID: 33486486
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rare GRN mutation in a patient diagnosed with primary progressive aphasia and  parkinsonism.
    Perković R; Jerčić KG; Frančić M; Ozretić D; Borovečki F
    Acta Neurol Belg; 2023 Apr; 123(2):727-729. PubMed ID: 35980504
    [No Abstract]   [Full Text] [Related]  

  • 11. The progranulin (GRN) Cys157LysfsX97 mutation is associated with nonfluent variant of primary progressive aphasia clinical phenotype.
    Caso F; Villa C; Fenoglio C; Santangelo R; Agosta F; Coppi E; Falautano M; Comi G; Filippi M; Scarpini E; Magnani G; Galimberti D
    J Alzheimers Dis; 2012; 28(4):759-63. PubMed ID: 22072213
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia.
    Cerami C; Marcone A; Galimberti D; Villa C; Fenoglio C; Scarpini E; Cappa SF
    J Alzheimers Dis; 2013; 36(3):415-20. PubMed ID: 23624518
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiency.
    Saracino D; Sellami L; Clot F; Camuzat A; Lamari F; Rucheton B; Benyounes I; Roué-Jagot C; Lagarde J; Sarazin M; Jornea L; Forlani S; LeGuern E; Dubois B; Brice A; Le Ber I
    Neurobiol Aging; 2020 Jan; 85():154.e9-154.e11. PubMed ID: 31262553
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Progranulin-associated primary progressive aphasia: a distinct phenotype?
    Rohrer JD; Crutch SJ; Warrington EK; Warren JD
    Neuropsychologia; 2010 Jan; 48(1):288-97. PubMed ID: 19766663
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frontotemporal Dementia due to the Novel GRN Arg161GlyfsX36 Mutation.
    Gazzina S; Archetti S; Alberici A; Bonomi E; Cosseddu M; Di Lorenzo D; Padovani A; Borroni B
    J Alzheimers Dis; 2017; 57(4):1185-1189. PubMed ID: 28304311
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Functional characterization of a novel progranulin mutation in a patient with progressive nonfluent aphasia.
    Gaweda-Walerych K; Sitek EJ; Narożańska E; Wezyk M; Brockhuis B; Zekanowski C; Sławek J
    Neurobiol Aging; 2018 Dec; 72():186.e9-186.e12. PubMed ID: 30057241
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Serum C-Peptide, Visfatin, Resistin, and Ghrelin are Altered in Sporadic and GRN-Associated Frontotemporal Lobar Degeneration.
    Zanardini R; Benussi L; Fostinelli S; Saraceno C; Ciani M; Borroni B; Padovani A; Binetti G; Ghidoni R
    J Alzheimers Dis; 2018; 61(3):1053-1060. PubMed ID: 29226876
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Missense mutation in GRN gene affecting RNA splicing and plasma progranulin level in a family affected by frontotemporal lobar degeneration.
    Luzzi S; Colleoni L; Corbetta P; Baldinelli S; Fiori C; Girelli F; Silvestrini M; Caroppo P; Giaccone G; Tagliavini F; Rossi G
    Neurobiol Aging; 2017 Jun; 54():214.e1-214.e6. PubMed ID: 28285794
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
    Le Ber I; Camuzat A; Hannequin D; Pasquier F; Guedj E; Rovelet-Lecrux A; Hahn-Barma V; van der Zee J; Clot F; Bakchine S; Puel M; Ghanim M; Lacomblez L; Mikol J; Deramecourt V; Lejeune P; de la Sayette V; Belliard S; Vercelletto M; Meyrignac C; Van Broeckhoven C; Lambert JC; Verpillat P; Campion D; Habert MO; Dubois B; Brice A;
    Brain; 2008 Mar; 131(Pt 3):732-46. PubMed ID: 18245784
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Variability of clinical syndromes and cerebral glucose metabolism in symptomatic frontotemporal lobar degeneration associated with progranulin mutations.
    Licata A; Grimmer T; Winkelmann J; Wagner M; Goldhardt O; Riedl L; Roßmeier C; Yakushev I; Diehl-Schmid J
    Amyotroph Lateral Scler Frontotemporal Degener; 2020 Aug; 21(5-6):389-395. PubMed ID: 32567375
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.