Recessive ataxias    -  Chairman:  Burk - Filla  

Filla A.             9.30-10.00 Recessive ataxias
Chessa L.       10.00-10.20 Ataxias associated with DNA repair
Brusco A.       10.20-10,40 8q24,3;xq translocation. Cerebellar hypoplasia and mental retardation
Molinari M.       10,40-11.00 Ataxia as action prediction failure: impact on treatment and neurorehabilitation 
Dominant ataxias  -  Chairman:  Giunti  - Taroni  

Taroni F.            11,30-12,00 The expanding field of “nonexpanded” dominant ataxias
Brunt E.             12,00-12,30 Cell biological and pathological results in polyq
Giunti P.            12,30-12,50 SCA 11
Orsi L.               12,50-13,10 SCA15 in italian families
Piacentini S.      13,10-13,30 Neuroimaging in hereditary ataxias

Treatment/Rehabilitation   -  Chairman:  Brunt - Pandolfo 15.00-18.00 

Pandolfo M.    HDAC inhibitors and Idebenone
Mariotti C.       Epo, Cepo and Deferipron
Saccà F.        Epo and lithium
Casali C.        Rehabilitation 
Sunday October 3, 2010    

Euroataxia session             9:00-12:30 

Pandolfo M./Mariotti/Burk    9:00-10:00 Efacts

Euroataxia assembly         10:00-12:30


Source AISA website

The legacy of Marie Schlau: literature to help cure Friedreich's Ataxia

If you feel like reading an unputdownable novel while collaborating with a just and solidary cause, "The Legacy of Marie Schlau" is your book! 100% of all funds raised will be dedicated to medical research to find a cure for Friedreich's Ataxia, a neurodegenerative disease that affects mostly young people, shortening their life expectancy and confining them to a wheelchair.

The life of Marie Schlau, a German Jewish girl born in 1833 hides great unsolved mysteries: accidents, disappearances, enigmas, unknown diagnoses, disturbing murders, love, tenderness, greed, lies, death ... alternatively a different story unfolds every time and takes us closer to the present. Thus, there are two parallel stories unravelling, each in a different age and place, which surprisingly converge in a revelatory chapter.

Paperback and Kindle versions for "The legacy of Marie Schlau" available for sale at Amazon now!


Research projects currently being financed by BabelFAmily

Currently, BabelFAmily is financing two promising research projects aimed at finding a cure for Friedreich's Ataxia. Whenever you make a donation to us or purchase a copy of "The legacy of Marie Schlau", this is where all funds raised will be devoted to:

1) Gene Therapy for Friedreich's Ataxia research project:

The project is the result of an initiative of Spanish people affected by this rare disease who are grouped in GENEFA in collaboration with the Spanish Federation of Ataxias and the BabelFAmily. The Friedreich’s Ataxia Research Alliance (FARA), one of the main patients’ associations in the United States now joins the endeavour.

2) Frataxin delivery research project:
The associations of patients and families Babel Family and the Asociación Granadina de la Ataxia de Friedreich (ASOGAF) channel 80,000 euros of their donations (50% from each organisation) into a new 18-month project at the Institute for Research in Biomedicine (IRB Barcelona). The project specifically aims to complete a step necessary in order to move towards a future frataxin replacement therapy for the brain, where the reduction of this protein causes the most damage in patients with Friedreich’s Ataxia.

The study is headed by Ernest Giralt, head of the Peptides and Proteins Lab, who has many years of experience and is a recognised expert in peptide chemistry and new systems of through which to delivery drugs to the brain, such as peptide shuttles—molecules that have the capacity to carry the drug across the barrier that surrounds and protects the brain. Since the lab started its relation with these patients’ associations in 2013*, it has been developing another two projects into Friedrich’s Ataxia.



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