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13. A novel missense mutation (L198R) in the Friedreich's ataxia gene. Al-Mahdawi S; Pook M; Chamberlain S Hum Mutat; 2000 Jul; 16(1):95. PubMed ID: 10874325 [No Abstract] [Full Text] [Related]
14. Friedreich's ataxia: a clinical and genetic analysis. Reddy PL; Grewal RP Clin Neurol Neurosurg; 2007 Feb; 109(2):200-2. PubMed ID: 17049722 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Early onset of Friedreich's ataxia in a compound heterozygote. McGovern MC; Stewart M; Morrison PJ; Webb D; Hawkins S Arch Dis Child; 2000 Jul; 83(1):74-5. PubMed ID: 10869006 [TBL] [Abstract][Full Text] [Related]
19. Friedreich's ataxia: clinical heterogeneity in two sisters. Armani M; Zortea M; Pastorello E; Lombardi S; Tonello S; Zuliani L; Rigoni MT; Trevisan CP Neurol Sci; 2006 Jun; 27(2):140-2. PubMed ID: 16816915 [TBL] [Abstract][Full Text] [Related]
20. Friedreich's ataxia: a new mutation in two compound heterozygous siblings with unusual clinical onset. Lamba LD; Ciotti P; Giribaldi G; Di Maria E; Varese A; Di Stadio M; Schenone A; Mandich P; Bellone E Eur Neurol; 2009; 61(4):240-3. PubMed ID: 19182486 [No Abstract] [Full Text] [Related] [Next] [New Search]