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 *

356 related articles for article (PubMed ID: 35576897)

  • 1. 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]  

  • 2. 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]  

  • 3. Estimated Prevalence and Incidence of Amyotrophic Lateral Sclerosis and SOD1 and C9orf72 Genetic Variants.
    Brown CA; Lally C; Kupelian V; Flanders WD
    Neuroepidemiology; 2021; 55(5):342-353. PubMed ID: 34247168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Seeding activity of human superoxide dismutase 1 aggregates in familial and sporadic amyotrophic lateral sclerosis postmortem neural tissues by real-time quaking-induced conversion.
    Mielke JK; Klingeborn M; Schultz EP; Markham EL; Reese ED; Alam P; Mackenzie IR; Ly CV; Caughey B; Cashman NR; Leavens MJ
    Acta Neuropathol; 2024 Jun; 147(1):100. PubMed ID: 38884646
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population.
    Chen YP; Yu SH; Wei QQ; Cao B; Gu XJ; Chen XP; Song W; Zhao B; Wu Y; Sun MM; Liu FF; Hou YB; Ou RW; Zhang LY; Liu KC; Lin JY; Xu XR; Li CY; Yang J; Jiang Z; Liu J; Cheng YF; Xiao Y; Chen K; Feng F; Cai YY; Li SR; Hu T; Yuan XQ; Guo XY; Liu H; Han Q; Zhou QQ; Shao N; Li JP; Pan PL; Ma S; Shang HF
    J Med Genet; 2022 Sep; 59(9):840-849. PubMed ID: 34544842
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Comprehensive analysis of the mutation spectrum in 301 German ALS families.
    Müller K; Brenner D; Weydt P; Meyer T; Grehl T; Petri S; Grosskreutz J; Schuster J; Volk AE; Borck G; Kubisch C; Klopstock T; Zeller D; Jablonka S; Sendtner M; Klebe S; Knehr A; Günther K; Weis J; Claeys KG; Schrank B; Sperfeld AD; Hübers A; Otto M; Dorst J; Meitinger T; Strom TM; Andersen PM; Ludolph AC; Weishaupt JH;
    J Neurol Neurosurg Psychiatry; 2018 Aug; 89(8):817-827. PubMed ID: 29650794
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The epidemiology and genetics of Amyotrophic lateral sclerosis in China.
    Liu X; He J; Gao FB; Gitler AD; Fan D
    Brain Res; 2018 Aug; 1693(Pt A):121-126. PubMed ID: 29501653
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and genetic characteristics of 1672 cases of amyotrophic lateral sclerosis in China: a single-center retrospective study.
    Shen D; Yang X; He D; Zhang K; Liu S; Sun X; Li J; Cai Z; Liu M; Zhang X; Liu Q; Cui L
    J Neurol; 2024 Aug; 271(8):5541-5548. PubMed ID: 38896262
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Generation of human induced pluripotent stem cell lines from sporadic, sporadic frontotemporal dementia, familial SOD1, and familial C9orf72 amyotrophic lateral sclerosis (ALS) patients.
    Jiang L; Tracey TJ; Gill MK; Howe SL; Power DT; Bharti V; McCombe PA; Henderson RD; Steyn FJ; Ngo ST
    Stem Cell Res; 2024 Aug; 78():103447. PubMed ID: 38796984
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis.
    Stoccoro A; Smith AR; Mosca L; Marocchi A; Gerardi F; Lunetta C; Cereda C; Gagliardi S; Lunnon K; Migliore L; Coppedè F
    Clin Epigenetics; 2020 Sep; 12(1):137. PubMed ID: 32917270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dysregulation of AMPA receptor subunit expression in sporadic ALS post-mortem brain.
    Gregory JM; Livesey MR; McDade K; Selvaraj BT; Barton SK; Chandran S; Smith C
    J Pathol; 2020 Jan; 250(1):67-78. PubMed ID: 31579943
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reduced penetrance of gene variants causing amyotrophic lateral sclerosis.
    Douglas AGL; Baralle D
    J Med Genet; 2024 Feb; 61(3):294-297. PubMed ID: 38123999
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders.
    Olsen CG; Busk ØL; Holla ØL; Tveten K; Holmøy T; Tysnes OB; Høyer H
    Amyotroph Lateral Scler Frontotemporal Degener; 2024 Feb; 25(1-2):177-187. PubMed ID: 37849306
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetics of amyotrophic lateral sclerosis.
    Corcia P; Couratier P; Blasco H; Andres CR; Beltran S; Meininger V; Vourc'h P
    Rev Neurol (Paris); 2017 May; 173(5):254-262. PubMed ID: 28449881
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Advantages of routine next-generation sequencing over standard genetic testing in the amyotrophic lateral sclerosis clinic.
    Scaber J; Thompson AG; Farrimond L; Feneberg E; Proudfoot M; Ossher L; Turner MR; Talbot K
    Eur J Neurol; 2023 Aug; 30(8):2240-2249. PubMed ID: 37159497
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis.
    Nishiyama A; Niihori T; Warita H; Izumi R; Akiyama T; Kato M; Suzuki N; Aoki Y; Aoki M
    Neurobiol Aging; 2017 May; 53():194.e1-194.e8. PubMed ID: 28160950
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.