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 *

188 related articles for article (PubMed ID: 23859338)

  • 1. Prevalence gradients of Friedreich's ataxia and R1b haplotype in Europe co-localize, suggesting a common Palaeolithic origin in the Franco-Cantabrian ice age refuge.
    Vankan P
    J Neurochem; 2013 Aug; 126 Suppl 1():11-20. PubMed ID: 23859338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population.
    Zeng J; Wang J; Zeng S; He M; Zeng X; Zhou Y; Liu Z; Jiang H; Tang B
    J Neurol Sci; 2015 Apr; 351(1-2):124-126. PubMed ID: 25765228
    [TBL] [Abstract][Full Text] [Related]  

  • 4. North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion.
    Singh I; Faruq M; Mukherjee O; Jain S; Pal PK; Srivastav MV; Behari M; Srivastava AK; Mukerji M
    Ann Hum Genet; 2010 May; 74(3):202-10. PubMed ID: 20374234
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity.
    Sirugo G; Cocozza S; Brice A; Cavalcanti F; De Michele G; Dones I; Filla A; Koenig M; Lorenzetti D; Monticelli A
    Eur J Hum Genet; 1993; 1(2):133-43. PubMed ID: 7914465
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective.
    Koutsis G; Kladi A; Karadima G; Houlden H; Wood NW; Christodoulou K; Panas M
    J Neurol Sci; 2014 Jan; 336(1-2):87-92. PubMed ID: 24209901
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population.
    Gómez M; Clark RM; Nath SK; Bhatti S; Sharma R; Alonso E; Rasmussen A; Bidichandani SI
    Genomics; 2004 Nov; 84(5):779-84. PubMed ID: 15475256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Clinical and Epidemiological Prevalence Study on Friedreich's Ataxia in Latium, Italy.
    Romano S; Bacigalupo I; Marcotulli C; Cioffi E; Bertini ES; Vasco G; Perna A; Petrucci A; Massa R; Frezza E; Romano C; Salvetti M; Ristori G; Silvestri G; Vanacore N; Casali C
    Neuroepidemiology; 2022; 56(3):212-218. PubMed ID: 35636410
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity.
    Christodoulou K; Deymeer F; Serdaroğlu P; Ozdemir C; Poda M; Georgiou DM; Ioannou P; Tsingis M; Zamba E; Middleton LT
    Neurogenetics; 2001 Jul; 3(3):127-32. PubMed ID: 11523563
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nonataxia symptoms in Friedreich Ataxia: Report from the Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS).
    Reetz K; Dogan I; Hohenfeld C; Didszun C; Giunti P; Mariotti C; Durr A; Boesch S; Klopstock T; Rodríguez de Rivera Garrido FJ; Schöls L; Giordano I; Bürk K; Pandolfo M; Schulz JB;
    Neurology; 2018 Sep; 91(10):e917-e930. PubMed ID: 30097477
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Friedreich's ataxia GAA repeat expansion in patients with recessive or sporadic ataxia.
    Geschwind DH; Perlman S; Grody WW; Telatar M; Montermini L; Pandolfo M; Gatti RA
    Neurology; 1997 Oct; 49(4):1004-9. PubMed ID: 9339680
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Friedreich Ataxia: Diagnostic Yield and Minimal Frequency in South Brazil.
    Fussiger H; Saraiva-Pereira ML; Leistner-Segal S; Jardim LB
    Cerebellum; 2019 Feb; 18(1):147-151. PubMed ID: 29938355
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The expanded mtDNA phylogeny of the Franco-Cantabrian region upholds the pre-neolithic genetic substrate of Basques.
    Cardoso S; Valverde L; Alfonso-Sánchez MA; Palencia-Madrid L; Elcoroaristizabal X; Algorta J; Catarino S; Arteta D; Herrera RJ; Zarrabeitia MT; Peña JA; de Pancorbo MM
    PLoS One; 2013; 8(7):e67835. PubMed ID: 23844106
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western Europe.
    Myres NM; Rootsi S; Lin AA; Järve M; King RJ; Kutuev I; Cabrera VM; Khusnutdinova EK; Pshenichnov A; Yunusbayev B; Balanovsky O; Balanovska E; Rudan P; Baldovic M; Herrera RJ; Chiaroni J; Di Cristofaro J; Villems R; Kivisild T; Underhill PA
    Eur J Hum Genet; 2011 Jan; 19(1):95-101. PubMed ID: 20736979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Friedreich's disease. A linkage study in southern and central Italy.
    Cavalcanti F; Cocozza S; Filla A; De Michele G; Pianese L; Porcellini A; Monticelli A; Pandolfo M; Banfi S; Varrone S
    Acta Neurol (Napoli); 1992; 14(4-6):519-23. PubMed ID: 1363458
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Frequency and Genetic Profile of Compound Heterozygous Friedreich's Ataxia Patients-the Brazilian Experience.
    Peluzzo TM; Bonadia LC; Donatti A; Molck MC; Jardim LB; Marques W; Lopes-Cendes IT; França MC
    Cerebellum; 2019 Dec; 18(6):1143-1146. PubMed ID: 31243663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.