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 *

117 related articles for article (PubMed ID: 33612544)

  • 21. 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]  

  • 22. Cerebrospinal fluid soluble TREM2 levels in frontotemporal dementia differ by genetic and pathological subgroup.
    Woollacott IOC; Nicholas JM; Heslegrave A; Heller C; Foiani MS; Dick KM; Russell LL; Paterson RW; Keshavan A; Fox NC; Warren JD; Schott JM; Zetterberg H; Rohrer JD
    Alzheimers Res Ther; 2018 Aug; 10(1):79. PubMed ID: 30111356
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Amyotrophic lateral sclerosis with primary progressive aphasia: a case report and literature review.
    Zhang A; Xu H; Huang J; Guo S; Tian T; Lei X; He D
    Neuro Endocrinol Lett; 2022 Dec; 43(6):293-302. PubMed ID: 36586129
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 20(2):240-249. PubMed ID: 28749476
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia.
    Kim EJ; Kwon JC; Park KH; Park KW; Lee JH; Choi SH; Jeong JH; Kim BC; Yoon SJ; Yoon YC; Kim S; Park KC; Choi BO; Na DL; Ki CS; Kim SH
    Neurobiol Aging; 2014 May; 35(5):1213.e13-7. PubMed ID: 24387985
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic predictors of survival in behavioral variant frontotemporal degeneration.
    Caswell C; McMillan CT; Xie SX; Van Deerlin VM; Suh E; Lee EB; Trojanowski JQ; Lee VM; Irwin DJ; Grossman M; Massimo LM
    Neurology; 2019 Oct; 93(18):e1707-e1714. PubMed ID: 31537715
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Frontotemporal dementia.
    Deleon J; Miller BL
    Handb Clin Neurol; 2018; 148():409-430. PubMed ID: 29478591
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Genetics of dementia in a Finnish cohort.
    Pasanen P; Myllykangas L; Pöyhönen M; Kiviharju A; Siitonen M; Hardy J; Bras J; Paetau A; Tienari PJ; Guerreiro R; Verkkoniemi-Ahola A
    Eur J Hum Genet; 2018 Jun; 26(6):827-837. PubMed ID: 29476165
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The
    Rossi G; Salvi E; Benussi L; Mehmeti E; Geviti A; Bellini S; Longobardi A; Facconi A; Carrara M; Bonvicini C; Nicsanu R; Saraceno C; Ricci M; Giaccone G; Binetti G; Ghidoni R
    Int J Mol Sci; 2022 Oct; 23(21):. PubMed ID: 36361641
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
    Rademakers R; Baker M; Gass J; Adamson J; Huey ED; Momeni P; Spina S; Coppola G; Karydas AM; Stewart H; Johnson N; Hsiung GY; Kelley B; Kuntz K; Steinbart E; Wood EM; Yu CE; Josephs K; Sorenson E; Womack KB; Weintraub S; Pickering-Brown SM; Schofield PR; Brooks WS; Van Deerlin VM; Snowden J; Clark CM; Kertesz A; Boylan K; Ghetti B; Neary D; Schellenberg GD; Beach TG; Mesulam M; Mann D; Grafman J; Mackenzie IR; Feldman H; Bird T; Petersen R; Knopman D; Boeve B; Geschwind DH; Miller B; Wszolek Z; Lippa C; Bigio EH; Dickson D; Graff-Radford N; Hutton M
    Lancet Neurol; 2007 Oct; 6(10):857-68. PubMed ID: 17826340
    [TBL] [Abstract][Full Text] [Related]  

  • 32. C9ORF72 hexanucleotide repeat expansion frequency in patients with Paget's disease of bone.
    Rubino E; Di Stefano M; Galimberti D; Serpente M; Scarpini E; Fenoglio C; Bo M; Rainero I
    Neurobiol Aging; 2020 Jan; 85():154.e1-154.e3. PubMed ID: 31530427
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Screening of dementia genes by whole-exome sequencing in Spanish patients with early-onset dementia: likely pathogenic, uncertain significance and risk variants.
    Ramos-Campoy O; Antonell A; Falgàs N; Balasa M; Borrego-Écija S; Rodríguez-Santiago B; Datta D; Armengol L; Fernández-Villullas G; Bosch B; Olives J; Muñoz-García C; Castellví M; Tort-Merino A; Sánchez-Valle R; Lladó A
    Neurobiol Aging; 2020 Sep; 93():e1-e9. PubMed ID: 32317127
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia.
    Lashley T; Rohrer JD; Mahoney C; Gordon E; Beck J; Mead S; Warren J; Rossor M; Revesz T
    Neuropathol Appl Neurobiol; 2014 Jun; 40(4):502-13. PubMed ID: 24286341
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
    Gallagher MD; Suh E; Grossman M; Elman L; McCluskey L; Van Swieten JC; Al-Sarraj S; Neumann M; Gelpi E; Ghetti B; Rohrer JD; Halliday G; Van Broeckhoven C; Seilhean D; Shaw PJ; Frosch MP; Alafuzoff I; Antonell A; Bogdanovic N; Brooks W; Cairns NJ; Cooper-Knock J; Cotman C; Cras P; Cruts M; De Deyn PP; DeCarli C; Dobson-Stone C; Engelborghs S; Fox N; Galasko D; Gearing M; Gijselinck I; Grafman J; Hartikainen P; Hatanpaa KJ; Highley JR; Hodges J; Hulette C; Ince PG; Jin LW; Kirby J; Kofler J; Kril J; Kwok JB; Levey A; Lieberman A; Llado A; Martin JJ; Masliah E; McDermott CJ; McKee A; McLean C; Mead S; Miller CA; Miller J; Munoz DG; Murrell J; Paulson H; Piguet O; Rossor M; Sanchez-Valle R; Sano M; Schneider J; Silbert LC; Spina S; van der Zee J; Van Langenhove T; Warren J; Wharton SB; White CL; Woltjer RL; Trojanowski JQ; Lee VM; Van Deerlin V; Chen-Plotkin AS
    Acta Neuropathol; 2014 Mar; 127(3):407-18. PubMed ID: 24442578
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation.
    Gliebus G; Bigio EH; Gasho K; Mishra M; Caplan D; Mesulam MM; Geula C
    Neurology; 2010 May; 74(20):1607-10. PubMed ID: 20479359
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.
    Mann DMA; Snowden JS
    Brain Pathol; 2017 Nov; 27(6):723-736. PubMed ID: 28100023
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.