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You searched for: Author/Creator Turon‐Sans, Janina

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1. A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction?. Issue 1 (22nd December 2020)

2. Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease. (11th January 2023)

3. Clinical characteristics and outcomes of thymoma‐associated myasthenia gravis. (30th March 2021)

4. Cognitive decline in amyotrophic lateral sclerosis: Neuropathological substrate and genetic determinants. (12th February 2021)

5. Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation. (10th January 2021)

6. Drug‐refractory myasthenia gravis: Clinical characteristics, treatments, and outcome. Issue 2 (26th January 2022)

8. The Sant Pau Initiative on Neurodegeneration (SPIN) cohort: A data set for biomarker discovery and validation in neurodegenerative disorders. Issue 1 (1st January 2019)