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1. A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss. Issue 11 (10th October 2016)

2. A Roma founder BIN1 mutation causes a novel phenotype of centronuclear myopathy with rigid spine. (24th July 2018)

3. Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide. Issue 1 (11th October 2012)

4. Assessing Dysferlinopathy Patients Over Three Years With a New Motor Scale. Issue 5 (26th February 2021)

5. Assessment of disease progression in dysferlinopathy: A 1-year cohort study. (29th January 2019)

6. Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study. Issue 5 (5th March 2022)

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

8. Charcot–Marie–Tooth disease due to MORC2 mutations in Spain. (18th July 2021)

9. Clinical and therapeutic features of myasthenia gravis in adults based on age at onset. (17th March 2020)

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