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Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.
Parkinsonism Relat Disord. 2014 Aug;20(8):919-23. doi: 10.1016/j.parkreldis.2014.04.018. Epub 2014 Apr 26.
Parkinsonism Relat Disord. 2014.
PMID: 24816001
Erythropoietin in Friedreich ataxia: no effect on frataxin in a randomized controlled trial.
Mariotti C, Fancellu R, Caldarazzo S, Nanetti L, Di Bella D, Plumari M, Lauria G, Cappellini MD, Duca L, Solari A, Taroni F.
Mariotti C, et al. Among authors: caldarazzo s.
Mov Disord. 2012 Mar;27(3):446-9. doi: 10.1002/mds.24066. Epub 2012 Jan 4.
Mov Disord. 2012.
PMID: 22411849
Clinical Trial.
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Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.
Di Bella D, Pareyson D, Savoiardo M, Farina L, Ciano C, Caldarazzo S, Sagnelli A, Bonato S, Nava S, Bresolin N, Tedeschi G, Taroni F, Salsano E.
Di Bella D, et al. Among authors: caldarazzo s.
Neurology. 2014 Sep 23;83(13):1217-8. doi: 10.1212/WNL.0000000000000812. Epub 2014 Aug 15.
Neurology. 2014.
PMID: 25128180
Free article.
No abstract available.
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Unscrambling thermal stability and temperature adaptation in evolved variants of a cold-active lipase.
Gatti-Lafranconi P, Caldarazzo SM, Villa A, Alberghina L, Lotti M.
Gatti-Lafranconi P, et al. Among authors: caldarazzo sm.
FEBS Lett. 2008 Jun 25;582(15):2313-8. doi: 10.1016/j.febslet.2008.05.037. Epub 2008 Jun 4.
FEBS Lett. 2008.
PMID: 18534193
Free article.
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