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2. Charcot‐Marie‐Tooth disease: frequency of genetic subtypes in a Southern Italy population. Issue 4 (December 2014)

3. Expanding the spectrum of genes responsible for hereditary motor neuropathies. Issue 10 (5th June 2019)

4. Frequency, entity and determinants of fatigue in Charcot–Marie–Tooth disease. (2nd December 2022)

6. Mutations in MYO9B are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy. (21st November 2022)

7. Novel mutations in dystonin provide clues to the pathomechanisms of HSAN-VI. (30th May 2017)

9. Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry. (15th December 2020)