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 *

120 related articles for article (PubMed ID: 9091786)

  • 1. Genetic abnormalities in Friedreich's ataxia.
    Filla A; De Michele G; Cocozza S
    N Engl J Med; 1997 Apr; 336(14):1021-2; author reply 1022. PubMed ID: 9091786
    [No Abstract]   [Full Text] [Related]  

  • 2. Friedreich's ataxia. Revision of the phenotype according to molecular genetics.
    Schöls L; Amoiridis G; Przuntek H; Frank G; Epplen JT; Epplen C
    Brain; 1997 Dec; 120 ( Pt 12)():2131-40. PubMed ID: 9448568
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features.
    Illarioshkin SN; Bagieva GK; Klyushnikov SA; Ovchinnikov IV; Markova ED; Ivanova-Smolenskaya IA
    Eur J Neurol; 2000 Sep; 7(5):535-40. PubMed ID: 11054139
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular analysis of Friedreich's ataxia locus in the Indian population.
    Mukerji M; Choudhry S; Saleem Q; Padma MV; Maheshwari MC; Jain S
    Acta Neurol Scand; 2000 Oct; 102(4):227-9. PubMed ID: 11071107
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic abnormalities in Friedreich's ataxia.
    Dutka DP; Nunez DJ
    N Engl J Med; 1997 Apr; 336(14):1021; author reply 1022. PubMed ID: 9091785
    [No Abstract]   [Full Text] [Related]  

  • 6. Challenges ahead for trials in Friedreich's ataxia.
    Lynch DR; Kichula E
    Lancet Neurol; 2016 Dec; 15(13):1300-1301. PubMed ID: 27839636
    [No Abstract]   [Full Text] [Related]  

  • 7. Marked variation in the cardiomyopathy associated with Friedreich's ataxia.
    Dutka DP; Donnelly JE; Nihoyannopoulos P; Oakley CM; Nunez DJ
    Heart; 1999 Feb; 81(2):141-7. PubMed ID: 9922348
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic abnormalities in Friedreich's ataxia.
    Madhani HD
    N Engl J Med; 1997 Apr; 336(14):1022; author reply 1022-3. PubMed ID: 9091787
    [No Abstract]   [Full Text] [Related]  

  • 9. GAA expansion size and age at onset of Friedreich's ataxia.
    Mateo I; Llorca J; Volpini V; Corral J; Berciano J; Combarros O
    Neurology; 2003 Jul; 61(2):274-5. PubMed ID: 12874424
    [No Abstract]   [Full Text] [Related]  

  • 10. Trinucleotide (GAA)n repeat expansion in two families with Friedreich's ataxia with retained reflexes.
    Kellett MW; Fletcher NA; Wood N; Enevoldson TP
    J Neurol Neurosurg Psychiatry; 1997 Dec; 63(6):780-3. PubMed ID: 9416816
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and genetic abnormalities in patients with Friedreich's ataxia.
    Dürr A; Cossee M; Agid Y; Campuzano V; Mignard C; Penet C; Mandel JL; Brice A; Koenig M
    N Engl J Med; 1996 Oct; 335(16):1169-75. PubMed ID: 8815938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The GAA repeat expansion in intron 1 of the frataxin gene is related to the severity of cardiac manifestation in patients with Friedreich's ataxia.
    Bit-Avragim N; Perrot A; Schöls L; Hardt C; Kreuz FR; Zühlke C; Bubel S; Laccone F; Vogel HP; Dietz R; Osterziel KJ
    J Mol Med (Berl); 2001; 78(11):626-32. PubMed ID: 11269509
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GAA trinucleotide repeat expansion in variant Friedreich's ataxia families.
    Cruz-Martínez A; Anciones B; Palau F
    Muscle Nerve; 1997 Sep; 20(9):1121-6. PubMed ID: 9270667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.
    Reetz K; Dogan I; Costa AS; Dafotakis M; Fedosov K; Giunti P; Parkinson MH; Sweeney MG; Mariotti C; Panzeri M; Nanetti L; Arpa J; Sanz-Gallego I; Durr A; Charles P; Boesch S; Nachbauer W; Klopstock T; Karin I; Depondt C; vom Hagen JM; Schöls L; Giordano IA; Klockgether T; Bürk K; Pandolfo M; Schulz JB
    Lancet Neurol; 2015 Feb; 14(2):174-82. PubMed ID: 25566998
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.
    De Castro M; García-Planells J; Monrós E; Cañizares J; Vázquez-Manrique R; Vílchez JJ; Urtasun M; Lucas M; Navarro G; Izquierdo G; Moltó MD; Palau F
    Hum Genet; 2000 Jan; 106(1):86-92. PubMed ID: 10982187
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of Friedreich's ataxia confirmed by DNA-analysis.
    Atanassov N; Markova V
    Folia Med (Plovdiv); 1998; 40(3):11-3. PubMed ID: 10658348
    [TBL] [Abstract][Full Text] [Related]  

  • 17. GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases.
    Gacy AM; Goellner GM; Spiro C; Chen X; Gupta G; Bradbury EM; Dyer RB; Mikesell MJ; Yao JZ; Johnson AJ; Richter A; Melançon SB; McMurray CT
    Mol Cell; 1998 Mar; 1(4):583-93. PubMed ID: 9660942
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Safety and efficacy of interferon γ in friedreich's ataxia.
    Vavla M; D'Angelo MG; Arrigoni F; Toschi N; Peruzzo D; Gandossini S; Russo A; Diella E; Tirelli S; Salati R; Scarpazza P; Luffarelli R; Fortuni S; Rufini A; Condò I; Testi R; Martinuzzi A
    Mov Disord; 2020 Feb; 35(2):370-371. PubMed ID: 31930551
    [No Abstract]   [Full Text] [Related]  

  • 19. Intronic GAA triplet repeat expansion in Friedreich's ataxia presenting with pure sensory ataxia.
    Berciano J; Combarros O; De Castro M; Palau F
    J Neurol; 1997 Jun; 244(6):390-1. PubMed ID: 9249627
    [No Abstract]   [Full Text] [Related]  

  • 20. Friedreich's ataxia: clinical aspects and pathogenesis.
    Pandolfo M
    Semin Neurol; 1999; 19(3):311-21. PubMed ID: 12194387
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.