HDACi Correct Frataxin Deficiency in a FA Mouse Model, April 9, 2008
Antioxidant Therapy in Inherited Ataxias by Massimo Pandolfo, 03/25/2008
Latest news on Friedreich’s Ataxia therapeutic approaches, gofar, October 2007
FA Research update by FARA's president (april 2006)
Friedreich Ataxia, an overview #1
Friedreich ataxia: an overview #2
MDA's Friedreich Ataxia information (extensive)
Recombinant human erythropoietin: effects on frataxin expression in vitro - July 2005
Friedreich ataxia, the oxidative stress paradox - December 2004
Friedreich’s ataxia – yesterday, today and tomorrow - Neurol India 2003;51:176-182
Finaly a mouse model for Friedreich ataxia - February 2001
Another article on the FA mouse model - January 2001
PRE-NATAL diagnosis of Friedreich's Ataxia - January 2001
Increased levels of plasma malondialdehyde in Friedreich ataxia - December 2000
Friedreich Ataxia Research Update - Fall 2000
Friedreich ataxia: an overview - January 2000
Living with Friedreich's Ataxia
Molecular basis of FRDA-Pandolfo-technical - January 2000
FA Research Timeline ('96 to '98)
Friedreich's Ataxia hearing research
GeneClinics Reviews for Friedreich's Ataxia
GeneClinics Testing for Friedreich's Ataxia
GeneClinics Research for Friedreich's Ataxia
OMIM entry for FRDA (Friedreich's Ataxia)
OMIM entry for FRDA2 (Friedreich's Ataxia)
WUSTL entry for FRDA and FRDA2
Pediatric Database description of Friedreich's Ataxia
OMIM entry for AVED (Ataxia, Friedreich-like with Selective Vitamin E Deficiency):
Study reveals clues to Friedreich's Ataxia:
International Symposium On Inherited Ataxias
Science Online Frataxin And Iron Accumulation In The Mitochondria
Symposium in France paper on yeast and iron regulation
NIH Press Release Study May Reveal Clues to Friedreich's Ataxia
Pippets Parlour Good set of FA links by research student
Small FA survey results - 2001
Another MitoQ article - august 2003
Friedrich’s Ataxia drug breakthrough discovered (MitoQ) - january 2003
OMIM entry for AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY
GeneClinics Testing for ARSACS
ARSAL
autosomal recessive spastic ataxia with frequent leucoencephalopqathy
The A-T Appeal Ataxia-Telangiectasia group in the UK. (Glynis Watkins)
Pediatric Database description of A-T :
OMIM entry for A-T (Ataxia Telangiectasia):
GeneClinics Reviews for Ataxia-Telangiectasia Variant 1 (ATV1)
GeneClinics Research for Ataxia-Telangiectasia Variant 1 (ATV1)
GeneClinics Testing for Ataxia-Telangiectasia Variant 1 (ATV1)
OMIM entry for Spinocerebellar ataxia type 8 (A Recessive Infant-Onset Spinocerebellar Ataxia)