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 *

147 related articles for article (PubMed ID: 17522386)

  • 41. Conserved gene signatures shared among
    Minaya MA; Mahali S; Iyer AK; Eteleeb AM; Martinez R; Huang G; Budde J; Temple S; Nana AL; Seeley WW; Spina S; Grinberg LT; Harari O; Karch CM
    Front Mol Biosci; 2023; 10():1051494. PubMed ID: 36845551
    [No Abstract]   [Full Text] [Related]  

  • 42. Progranulin Mutations Affects Brain Oscillatory Activity in Fronto-Temporal Dementia.
    Moretti DV; Benussi L; Fostinelli S; Ciani M; Binetti G; Ghidoni R
    Front Aging Neurosci; 2016; 8():35. PubMed ID: 26973510
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Dissecting the Clinical Heterogeneity and Genotype-Phenotype Correlations of
    Villa C; Pellencin E; Romeo A; Giaccone G; Rossi G; Prioni S; Caroppo P
    Front Biosci (Landmark Ed); 2024 Jan; 29(1):12. PubMed ID: 38287807
    [TBL] [Abstract][Full Text] [Related]  

  • 44. An Autopsy Case of Familial Neuronal Intranuclear Inclusion Disease with Dementia and Neuropathy.
    Yamaguchi N; Mano T; Ohtomo R; Ishiura H; Almansour MA; Mori H; Kanda J; Shirota Y; Taira K; Morikawa T; Ikemura M; Yanagi Y; Murayama S; Shimizu J; Sakurai Y; Tsuji S; Iwata A
    Intern Med; 2018 Dec; 57(23):3459-3462. PubMed ID: 30101925
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
    Sone J; Mitsuhashi S; Fujita A; Mizuguchi T; Hamanaka K; Mori K; Koike H; Hashiguchi A; Takashima H; Sugiyama H; Kohno Y; Takiyama Y; Maeda K; Doi H; Koyano S; Takeuchi H; Kawamoto M; Kohara N; Ando T; Ieda T; Kita Y; Kokubun N; Tsuboi Y; Katoh K; Kino Y; Katsuno M; Iwasaki Y; Yoshida M; Tanaka F; Suzuki IK; Frith MC; Matsumoto N; Sobue G
    Nat Genet; 2019 Aug; 51(8):1215-1221. PubMed ID: 31332381
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mutations in PGRN gene associated with the risk of psoriasis in Pakistan: a case control study.
    Saleem S; Imran Z; Samdani A; Khoso B; Zehra S; Azhar A
    BMC Med Genomics; 2023 Dec; 16(1):335. PubMed ID: 38129828
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Pharmacotherapy for Frontotemporal Dementia.
    Khoury R; Liu Y; Sheheryar Q; Grossberg GT
    CNS Drugs; 2021 Apr; 35(4):425-438. PubMed ID: 33840052
    [TBL] [Abstract][Full Text] [Related]  

  • 48. SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus neuropathy.
    Klein CJ; Wu Y; Cunningham JM; Windebank AJ; Dyck PJ; Friedenberg SM; Klein DM; Dyck PJ
    Arch Neurol; 2009 Feb; 66(2):238-43. PubMed ID: 19204161
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Ribosomal protein SA is a common component of neuronal intranuclear inclusions in polyglutamine diseases and Marinesco bodies.
    Yagita K; Sadashima S; Koyama S; Noguchi H; Hamasaki H; Sasagasako N; Honda H
    Neuropathology; 2024 Feb; 44(1):31-40. PubMed ID: 37340992
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Neuropathology of cervical dystonia.
    Prudente CN; Pardo CA; Xiao J; Hanfelt J; Hess EJ; Ledoux MS; Jinnah HA
    Exp Neurol; 2013 Mar; 241():95-104. PubMed ID: 23195594
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Genetic Interactions of Progranulin Across the ALS-FTD Spectrum and Beyond.
    Doyle JJ; Parker JA
    MicroPubl Biol; 2023; 2023():. PubMed ID: 38188422
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Neuronal Intranuclear Inclusion Disease].
    Sone J; Sobue G
    Brain Nerve; 2017 Jan; 69(1):5-16. PubMed ID: 28126973
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Imaging prodromal FTD: seeing the future through PET crystals.
    Rabinovici GD; Boeve BF
    Neurology; 2013 Oct; 81(15):1282-3. PubMed ID: 24005338
    [No Abstract]   [Full Text] [Related]  

  • 54. The use of CRISPR to generate a whole-gene humanized
    Lins J; Hopkins CE; Brock T; Hart AC
    MicroPubl Biol; 2022; 2022():. PubMed ID: 36204657
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Neuropathological fingerprints of survival, atrophy and language in primary progressive aphasia.
    Mesulam MM; Coventry CA; Bigio EH; Sridhar J; Gill N; Fought AJ; Zhang H; Thompson CK; Geula C; Gefen T; Flanagan M; Mao Q; Weintraub S; Rogalski EJ
    Brain; 2022 Jun; 145(6):2133-2148. PubMed ID: 35441216
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Right temporal variant frontotemporal dementia is pathologically heterogeneous: a case-series and a systematic review.
    Ulugut H; Dijkstra AA; Scarioni M; ; Barkhof F; Scheltens P; Rozemuller AJM; Pijnenburg YAL
    Acta Neuropathol Commun; 2021 Aug; 9(1):131. PubMed ID: 34344452
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A clinical-radiological framework of the right temporal variant of frontotemporal dementia.
    Ulugut Erkoyun H; Groot C; Heilbron R; Nelissen A; van Rossum J; Jutten R; Koene T; van der Flier WM; Wattjes MP; Scheltens P; Ossenkoppele R; Barkhof F; Pijnenburg Y
    Brain; 2020 Sep; 143(9):2831-2843. PubMed ID: 32830218
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Progranulin: Functions and neurologic correlations.
    Townley RA; Boeve BF; Benarroch EE
    Neurology; 2018 Jan; 90(3):118-125. PubMed ID: 29263224
    [No Abstract]   [Full Text] [Related]  

  • 59. Dysexecutive mild cognitive impairment associated to frontal atrophy: Case report.
    Balthazar MLF; Damasceno BP
    Dement Neuropsychol; 2008; 2(1):76-79. PubMed ID: 29213545
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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 8.