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 *

138 related articles for article (PubMed ID: 26465287)

  • 21. C9ORF72 familial motor neuron disease - frontotemporal dementia associated with lung adenocarcinoma and anti-Ma2/Ta antibodies: a chance association?
    Geevasinga N; Burrell JR; Hibbert M; Vucic S; Ng K
    Eur J Neurol; 2014 Apr; 21(4):e31-3. PubMed ID: 24628901
    [No Abstract]   [Full Text] [Related]  

  • 22. Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosis.
    Byrne S; Heverin M; Elamin M; Bede P; Lynch C; Kenna K; MacLaughlin R; Walsh C; Al Chalabi A; Hardiman O
    Ann Neurol; 2013 Nov; 74(5):699-708. PubMed ID: 23836460
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion.
    Luigetti M; Quaranta D; Conte A; Piccininni C; Lattante S; Romano A; Silvestri G; Zollino M; Sabatelli M
    Amyotroph Lateral Scler Frontotemporal Degener; 2013 Jan; 14(1):66-9. PubMed ID: 22708871
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Rapidly progressive frontotemporal dementia and bulbar amyotrophic lateral sclerosis in Portuguese patients with C9orf72 mutation.
    Chester C; de Carvalho M; Miltenberger G; Pereira S; Dillen L; van der Zee J; van Broeckhoven C; de Mendonça A
    Amyotroph Lateral Scler Frontotemporal Degener; 2013 Jan; 14(1):70-2. PubMed ID: 22742426
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.
    Siddique T; Figlewicz DA; Pericak-Vance MA; Haines JL; Rouleau G; Jeffers AJ; Sapp P; Hung WY; Bebout J; McKenna-Yasek D
    N Engl J Med; 1991 May; 324(20):1381-4. PubMed ID: 2020294
    [TBL] [Abstract][Full Text] [Related]  

  • 26. C9orf72 hexanucleotide repeat expansions as the causative mutation for chromosome 9p21-linked amyotrophic lateral sclerosis and frontotemporal dementia.
    Daoud H; Suhail H; Sabbagh M; Belzil V; Szuto A; Dionne-Laporte A; Khoris J; Camu W; Salachas F; Meininger V; Mathieu J; Strong M; Dion PA; Rouleau GA
    Arch Neurol; 2012 Sep; 69(9):1159-63. PubMed ID: 22964911
    [TBL] [Abstract][Full Text] [Related]  

  • 27. ALS: Recent Developments from Genetics Studies.
    Therrien M; Dion PA; Rouleau GA
    Curr Neurol Neurosci Rep; 2016 Jun; 16(6):59. PubMed ID: 27113253
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study.
    Debray S; Race V; Crabbé V; Herdewyn S; Matthijs G; Goris A; Dubois B; Thijs V; Robberecht W; Van Damme P
    Neurobiol Aging; 2013 Dec; 34(12):2890.e7-2890.e12. PubMed ID: 23870417
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Criteria for diagnosis of familial amyotrophic lateral sclerosis. European FALS Collaborative Group.
    Swash M; Leigh N
    Neuromuscul Disord; 1992; 2(1):7-9. PubMed ID: 1356048
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The role of DNA damage response in amyotrophic lateral sclerosis.
    Sun Y; Curle AJ; Haider AM; Balmus G
    Essays Biochem; 2020 Oct; 64(5):847-861. PubMed ID: 33078197
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Amyotrophic lateral sclerosis.
    Younger DS; Brown RH
    Handb Clin Neurol; 2023; 196():203-229. PubMed ID: 37620070
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Amyotrophic Lateral Sclerosis Genetic Studies: From Genome-wide Association Mapping to Genome Sequencing.
    He J; Mangelsdorf M; Fan D; Bartlett P; Brown MA
    Neuroscientist; 2015 Dec; 21(6):599-615. PubMed ID: 25378359
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Clinical and neuroimaging characterization of two C9orf72-positive siblings with amyotrophic lateral sclerosis and schizophrenia.
    Vázquez-Costa JF; Beltrán E; Sopena P; Sabater A; Cardona F; Vilchez JJ; Pérez-Tur J; Sevilla T
    Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(3-4):297-300. PubMed ID: 26613114
    [No Abstract]   [Full Text] [Related]  

  • 34. Familial adult motor neuron disease: amyotrophic lateral sclerosis.
    Mulder DW; Kurland LT; Offord KP; Beard CM
    Neurology; 1986 Apr; 36(4):511-7. PubMed ID: 3960325
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Emerging insights into the complex genetics and pathophysiology of amyotrophic lateral sclerosis.
    Goutman SA; Hardiman O; Al-Chalabi A; Chió A; Savelieff MG; Kiernan MC; Feldman EL
    Lancet Neurol; 2022 May; 21(5):465-479. PubMed ID: 35334234
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Atypical forms of familial amyotrophic lateral sclerosis.
    Gregoire N; Serratrice G
    Adv Exp Med Biol; 1987; 209():159-64. PubMed ID: 3577907
    [No Abstract]   [Full Text] [Related]  

  • 37. Motor neuron disease: Brain transcriptome profiling reveals involvement of divergent pathways in C9orf72-associated and sporadic ALS.
    Malkki H
    Nat Rev Neurol; 2015 Sep; 11(9):484. PubMed ID: 26240037
    [No Abstract]   [Full Text] [Related]  

  • 38. CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis.
    Blair IP; Vance C; Durnall JC; Williams KL; Thoeng A; Shaw CE; Nicholson GA
    J Neurol Neurosurg Psychiatry; 2008 Jul; 79(7):849-50. PubMed ID: 18270236
    [No Abstract]   [Full Text] [Related]  

  • 39. Amyotrophic lateral sclerosis: a complex syndrome that needs an integrated research approach.
    Riancho J; Gil-Bea FJ; Santurtun A; López de Munaín A
    Neural Regen Res; 2019 Feb; 14(2):193-196. PubMed ID: 30530996
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Modelling amyotrophic lateral sclerosis in rodents.
    Todd TW; Petrucelli L
    Nat Rev Neurosci; 2022 Apr; 23(4):231-251. PubMed ID: 35260846
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.