BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

438 related articles for article (PubMed ID: 25123918)

  • 1. Genetic architecture of ALS in Sardinia.
    Borghero G; Pugliatti M; Marrosu F; Marrosu MG; Murru MR; Floris G; Cannas A; Parish LD; Occhineri P; Cau TB; Loi D; Ticca A; Traccis S; Manera U; Canosa A; Moglia C; Calvo A; Barberis M; Brunetti M; Pliner HA; Renton AE; Nalls MA; Traynor BJ; Restagno G; Chiò A;
    Neurobiol Aging; 2014 Dec; 35(12):2882.e7-2882.e12. PubMed ID: 25123918
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene.
    Chiò A; Borghero G; Pugliatti M; Ticca A; Calvo A; Moglia C; Mutani R; Brunetti M; Ossola I; Marrosu MG; Murru MR; Floris G; Cannas A; Parish LD; Cossu P; Abramzon Y; Johnson JO; Nalls MA; Arepalli S; Chong S; Hernandez DG; Traynor BJ; Restagno G;
    Arch Neurol; 2011 May; 68(5):594-8. PubMed ID: 21220647
    [TBL] [Abstract][Full Text] [Related]  

  • 3. ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations.
    Chiò A; Restagno G; Brunetti M; Ossola I; Calvo A; Canosa A; Moglia C; Floris G; Tacconi P; Marrosu F; Marrosu MG; Murru MR; Majounie E; Renton AE; Abramzon Y; Pugliatti M; Sotgiu MA; Traynor BJ; Borghero G;
    J Neurol Neurosurg Psychiatry; 2012 Jul; 83(7):730-3. PubMed ID: 22550220
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
    Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
    J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population.
    Vrabec K; Koritnik B; Leonardis L; Dolenc-Grošelj L; Zidar J; Smith B; Vance C; Shaw C; Rogelj B; Glavač D; Ravnik-Glavač M
    Neurobiol Aging; 2015 Mar; 36(3):1601.e17-20. PubMed ID: 25585530
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion.
    Chiò A; Mora G; Sabatelli M; Caponnetto C; Lunetta C; Traynor BJ; Johnson JO; Nalls MA; Calvo A; Moglia C; Borghero G; Trojsi F; La Bella V; Volanti P; Simone I; Salvi F; Logullo FO; Riva N; Carrera P; Giannini F; Mandrioli J; Tanel R; Capasso M; Tremolizzo L; Battistini S; Murru MR; Origone P; Zollino M; Penco S; ; ; Mazzini L; D'Alfonso S; Restagno G; Brunetti M; Barberis M; Conforti FL
    Neurobiol Aging; 2016 Mar; 39():218.e5-8. PubMed ID: 26733254
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Extensive genetics of ALS: a population-based study in Italy.
    Chiò A; Calvo A; Mazzini L; Cantello R; Mora G; Moglia C; Corrado L; D'Alfonso S; Majounie E; Renton A; Pisano F; Ossola I; Brunetti M; Traynor BJ; Restagno G;
    Neurology; 2012 Nov; 79(19):1983-9. PubMed ID: 23100398
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Disease survival and progression in TARDBP ALS patients from Sardinia, Italy.
    Borghero G; Pili F; Muroni A; Ercoli T; Pateri MI; Pilotto S; Maccabeo A; Defazio G
    J Neurol; 2024 Feb; 271(2):929-934. PubMed ID: 37855870
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
    Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V
    J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genotype-phenotype landscape of familial amyotrophic lateral sclerosis in Australia.
    McCann EP; Williams KL; Fifita JA; Tarr IS; O'Connor J; Rowe DB; Nicholson GA; Blair IP
    Clin Genet; 2017 Sep; 92(3):259-266. PubMed ID: 28105640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis.
    Soong BW; Lin KP; Guo YC; Lin CC; Tsai PC; Liao YC; Lu YC; Wang SJ; Tsai CP; Lee YC
    Neurobiol Aging; 2014 Oct; 35(10):2423.e1-6. PubMed ID: 24908169
    [TBL] [Abstract][Full Text] [Related]  

  • 14. TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
    Del Bo R; Ghezzi S; Corti S; Pandolfo M; Ranieri M; Santoro D; Ghione I; Prelle A; Orsetti V; Mancuso M; Sorarù G; Briani C; Angelini C; Siciliano G; Bresolin N; Comi GP
    Eur J Neurol; 2009 Jun; 16(6):727-32. PubMed ID: 19236453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic studies of Russian patients with amyotrophic lateral sclerosis.
    Lysogorskaia EV; Abramycheva NY; Zakharova MN; Stepanova MS; Moroz AA; Rossokhin AV; Illarioshkin SN
    Amyotroph Lateral Scler Frontotemporal Degener; 2015; 17(1-2):135-41. PubMed ID: 26551617
    [TBL] [Abstract][Full Text] [Related]  

  • 16. C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population.
    Sabatelli M; Conforti FL; Zollino M; Mora G; Monsurrò MR; Volanti P; Marinou K; Salvi F; Corbo M; Giannini F; Battistini S; Penco S; Lunetta C; Quattrone A; Gambardella A; Logroscino G; Simone I; Bartolomei I; Pisano F; Tedeschi G; Conte A; Spataro R; La Bella V; Caponnetto C; Mancardi G; Mandich P; Sola P; Mandrioli J; Renton AE; Majounie E; Abramzon Y; Marrosu F; Marrosu MG; Murru MR; Sotgiu MA; Pugliatti M; Rodolico C; ; Moglia C; Calvo A; Ossola I; Brunetti M; Traynor BJ; Borghero G; Restagno G; Chiò A
    Neurobiol Aging; 2012 Aug; 33(8):1848.e15-20. PubMed ID: 22418734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.
    Giannoccaro MP; Bartoletti-Stella A; Piras S; Pession A; De Massis P; Oppi F; Stanzani-Maserati M; Pasini E; Baiardi S; Avoni P; Parchi P; Liguori R; Capellari S
    J Neurol; 2017 Jul; 264(7):1426-1433. PubMed ID: 28620717
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.
    Bertolin C; D'Ascenzo C; Querin G; Gaiani A; Boaretto F; Salvoro C; Vazza G; Angelini C; Cagnin A; Pegoraro E; Sorarù G; Mostacciuolo ML
    Neurobiol Aging; 2014 May; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: the TARDBP Ala382Thr mutation and C9orf72 expansion.
    Lorefice L; Murru MR; Fenu G; Corongiu D; Frau J; Cuccu S; Coghe GC; Tranquilli S; Cocco E; Marrosu MG
    J Neurol Sci; 2015 Oct; 357(1-2):229-34. PubMed ID: 26233805
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.