Comorbidities in Friedreich ataxia: incidence and manifestations from early to advanced disease stages
Author:
Funder
Ministero della Salute
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-022-06360-w.pdf
Reference39 articles.
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2. Gellera C, Castellotti B, Mariotti C, Mineri R, Seveso V, Didonato S, Taroni F (2007) Frataxin gene point mutations in Italian Friedreich ataxia patients. Neurogenetics 8(4):289–299. https://doi.org/10.1007/s10048-007-0101-5
3. Evans-Galea MV, Carrodus N, Rowley SM, Corben LA, Tai G, Saffery R, Galati JC, Wong NC, Craig JM, Lynch DR et al (2012) FXN methylation predicts expression and clinical outcome in Friedreich ataxia. Ann Neurol 71(4):487–497. https://doi.org/10.1002/ana.22671
4. Parkinson MH, Boesch S, Nachbauer W, Mariotti C, Giunti P (2013) Clinical features of Friedreich’s ataxia: classical and atypical phenotypes. J Neurochem 126:103–117. https://doi.org/10.1111/jnc.12317
5. Cook A, Giunti P (2017) Friedreich’s ataxia: clinical features, pathogenesis and management. Br Med Bull 124(1):19–30. https://doi.org/10.1093/bmb/ldx034
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