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You searched for: Author/Creator Letournel, Franck

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1. Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A. (24th January 2017)

2. Expanding the spectrum of congenital myopathy linked to recessive mutations in SCN4A. (24th January 2017)

3. G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome. Issue 4 (21st May 2013)

4. Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4). Issue 9 (13th August 2018)

5. Metabolomics reveals highly regional specificity of cerebral sexual dimorphism in mice. (January 2020)

7. Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions. Issue 5 (3rd July 2018)