BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 37223130)

  • 1. Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.
    Ruf WP; Boros M; Freischmidt A; Brenner D; Grozdanov V; de Meirelles J; Meyer T; Grehl T; Petri S; Grosskreutz J; Weyen U; Guenther R; Regensburger M; Hagenacker T; Koch JC; Emmer A; Roediger A; Steinbach R; Wolf J; Weishaupt JH; Lingor P; Deschauer M; Cordts I; Klopstock T; Reilich P; Schoeberl F; Schrank B; Zeller D; Hermann A; Knehr A; Günther K; Dorst J; Schuster J; Siebert R; Ludolph AC; Müller K
    Brain Commun; 2023; 5(3):fcad152. PubMed ID: 37223130
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.
    Chiò A; Borghero G; Restagno G; Mora G; Drepper C; Traynor BJ; Sendtner M; Brunetti M; Ossola I; Calvo A; Pugliatti M; Sotgiu MA; Murru MR; Marrosu MG; Marrosu F; Marinou K; Mandrioli J; Sola P; Caponnetto C; Mancardi G; Mandich P; La Bella V; Spataro R; Conte A; Monsurrò MR; Tedeschi G; Pisano F; Bartolomei I; Salvi F; Lauria Pinter G; Simone I; Logroscino G; Gambardella A; Quattrone A; Lunetta C; Volanti P; Zollino M; Penco S; Battistini S; ; Renton AE; Majounie E; Abramzon Y; Conforti FL; Giannini F; Corbo M; Sabatelli M
    Brain; 2012 Mar; 135(Pt 3):784-93. PubMed ID: 22366794
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetics screening in an Italian cohort of patients with Amyotrophic Lateral Sclerosis: the importance of early testing and its implication.
    Libonati L; Cambieri C; Colavito D; Moret F; D'Andrea E; Del Giudice E; Leon A; Inghilleri M; Ceccanti M
    J Neurol; 2024 Apr; 271(4):1921-1936. PubMed ID: 38112783
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and genetic features of amyotrophic lateral sclerosis patients with
    Wiesenfarth M; Günther K; Müller K; Witzel S; Weiland U; Mayer K; Herrmann C; Brenner D; Schuster J; Freischmidt A; Lulé D; Meyer T; Regensburger M; Grehl T; Emmer A; Petri S; Großkreutz J; Rödiger A; Steinbach R; Klopstock T; Reilich P; Schöberl F; Wolf J; Hagenacker T; Weyen U; Zeller D; Ludolph AC; Dorst J
    Brain Commun; 2023; 5(2):fcad087. PubMed ID: 37006326
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic variability in sporadic amyotrophic lateral sclerosis.
    Van Daele SH; Moisse M; van Vugt JJFA; Zwamborn RAJ; van der Spek R; van Rheenen W; Van Eijk K; Kenna K; Corcia P; Vourc'h P; Couratier P; Hardiman O; McLaughin R; Gotkine M; Drory V; Ticozzi N; Silani V; Ratti A; de Carvalho M; Mora Pardina JS; Povedano M; Andersen PM; Weber M; Başak NA; Shaw C; Shaw PJ; Morrison KE; Landers JE; Glass JD; van Es MA; van den Berg LH; Al-Chalabi A; Veldink J; Van Damme P
    Brain; 2023 Sep; 146(9):3760-3769. PubMed ID: 37043475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.
    Cooper-Knock J; Hewitt C; Highley JR; Brockington A; Milano A; Man S; Martindale J; Hartley J; Walsh T; Gelsthorpe C; Baxter L; Forster G; Fox M; Bury J; Mok K; McDermott CJ; Traynor BJ; Kirby J; Wharton SB; Ince PG; Hardy J; Shaw PJ
    Brain; 2012 Mar; 135(Pt 3):751-64. PubMed ID: 22366792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Frequency of C9orf72 hexanucleotide repeat expansion and SOD1 mutations in Portuguese patients with amyotrophic lateral sclerosis.
    Gromicho M; Pinto S; Gisca E; Pronto-Laborinho AC; Andersen PM; de Carvalho M
    Neurobiol Aging; 2018 Oct; 70():325.e7-325.e15. PubMed ID: 29861044
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mild motor impairment as prodromal state in amyotrophic lateral sclerosis: a new diagnostic entity.
    Benatar M; Granit V; Andersen PM; Grignon AL; McHutchison C; Cosentino S; Malaspina A; Wuu J
    Brain; 2022 Oct; 145(10):3500-3508. PubMed ID: 35594156
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72.
    Boeve BF; Boylan KB; Graff-Radford NR; DeJesus-Hernandez M; Knopman DS; Pedraza O; Vemuri P; Jones D; Lowe V; Murray ME; Dickson DW; Josephs KA; Rush BK; Machulda MM; Fields JA; Ferman TJ; Baker M; Rutherford NJ; Adamson J; Wszolek ZK; Adeli A; Savica R; Boot B; Kuntz KM; Gavrilova R; Reeves A; Whitwell J; Kantarci K; Jack CR; Parisi JE; Lucas JA; Petersen RC; Rademakers R
    Brain; 2012 Mar; 135(Pt 3):765-83. PubMed ID: 22366793
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frequency of
    Yilmaz R; Grehl T; Eckrich L; Marschalkowski I; Weishaupt K; Valkadinov I; Simic M; Brenner D; Andersen PM; Wolf J; Weishaupt JH
    Amyotroph Lateral Scler Frontotemporal Degener; 2023 Aug; 24(5-6):414-419. PubMed ID: 36650645
    [No Abstract]   [Full Text] [Related]  

  • 11. The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.
    Simón-Sánchez J; Dopper EG; Cohn-Hokke PE; Hukema RK; Nicolaou N; Seelaar H; de Graaf JR; de Koning I; van Schoor NM; Deeg DJ; Smits M; Raaphorst J; van den Berg LH; Schelhaas HJ; De Die-Smulders CE; Majoor-Krakauer D; Rozemuller AJ; Willemsen R; Pijnenburg YA; Heutink P; van Swieten JC
    Brain; 2012 Mar; 135(Pt 3):723-35. PubMed ID: 22300876
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Apolipoprotein B-100-mediated motor neuron degeneration in sporadic amyotrophic lateral sclerosis.
    Wong JK; Roselle AK; Shue TM; Shimshak SJE; Beaty JM; Celestin NM; Gao I; Griffin RP; Cudkowicz ME; Sadiq SA
    Brain Commun; 2022; 4(4):fcac207. PubMed ID: 36043141
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS).
    Edgar S; Ellis M; Abdul-Aziz NA; Goh KJ; Shahrizaila N; Kennerson ML; Ahmad-Annuar A
    Neurobiol Aging; 2021 Dec; 108():200-206. PubMed ID: 34404558
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genotype-phenotype correlation in Tunisian patients with Amyotrophic Lateral Sclerosis.
    Kacem I; Sghaier I; Peverelli S; Souissi E; Ticozzi N; Gharbi A; Ratti A; Berrechid AG; Silani V; Gouider R
    Neurobiol Aging; 2022 Dec; 120():27-33. PubMed ID: 36108486
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis.
    Jang JH; Kwon MJ; Choi WJ; Oh KW; Koh SH; Ki CS; Kim SH
    Neurobiol Aging; 2013 Apr; 34(4):1311.e7-9. PubMed ID: 23088937
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic Epidemiology of Amyotrophic Lateral Sclerosis in Norway: A 2-Year Population-Based Study.
    Olsen CG; Busk ØL; Aanjesen TN; Alstadhaug KB; Bjørnå IK; Braathen GJ; Breivik KL; Demic N; Flemmen HØ; Hallerstig E; HogenEsch I; Holla ØL; Jøntvedt AB; Kampman MT; Kleveland G; Kvernmo HB; Ljøstad U; Maniaol A; Morsund ÅH; Nakken O; Novy C; Rekand T; Schlüter K; Schüler S; Tveten K; Tysnes OB; Holmøy T; Høyer H
    Neuroepidemiology; 2022; 56(4):271-282. PubMed ID: 35576897
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort.
    Krüger S; Battke F; Sprecher A; Munz M; Synofzik M; Schöls L; Gasser T; Grehl T; Prudlo J; Biskup S
    Front Mol Neurosci; 2016; 9():92. PubMed ID: 27790088
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK.
    Kwok CT; Wang HY; Morris AG; Smith B; Shaw C; de Belleroche J
    J Neurol Sci; 2015 Feb; 349(1-2):209-13. PubMed ID: 25618255
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia.
    Yang X; Sun X; Liu Q; Liu L; Li J; Cai Z; Zhang K; Liu S; He D; Shen D; Liu M; Cui L; Zhang X
    Orphanet J Rare Dis; 2022 Nov; 17(1):404. PubMed ID: 36345033
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.