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1. No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland. Issue 7 (December 2013)

2. The Swedish motor neuron disease quality registry. Issue 7 (2nd October 2018)

3. Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small‐fiber and mixed neuropathy. Issue 3 (4th December 2018)

5. Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy. (April 2021)

8. Cardiac troponin T is elevated and increases longitudinally in ALS patients. Issue 1 (2nd January 2022)