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3. A cross‐sectional, prospective ocular motor study in 72 patients with Niemann‐Pick disease type C. (12th July 2021)

4. A slowly progressive mitochondrial encephalomyopathy widens the spectrum of AIFM1 disorders. (26th May 2015)

9. From congenital microcephaly to adult onset cerebellar ataxia: Distinct and overlapping phenotypes in patients with PNKP gene mutations. Issue 11 (22nd August 2019)

10. Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy. Issue 1 (March 2017)