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You searched for: Author/Creator Bresolin, Nereo

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1. A de novo C19orf12 heterozygous mutation in a patient with MPAN. (March 2018)

2. A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia. Issue 4 (2nd February 2021)

3. A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. Issue 8 (3rd August 2010)

5. Anti-sulfatide reactivity in patients with celiac disease. (3rd April 2017)

6. Assessing mental health in boys with Duchenne muscular dystrophy: Emotional, behavioural and neurodevelopmental profile in an Italian clinical sample. (July 2017)

8. Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations. Issue 5 (4th May 2021)