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1. Abnormal spontaneous activity in primary myopathic disorders. Issue 3 (17th June 2017)

2. Andersen–Tawil syndrome: Report of 3 novel mutations and high risk of symptomatic cardiac involvement. Issue 2 (19th November 2014)

3. Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?. Issue 1 (March 2016)

4. Clinical, electrophysiological, and molecular findings in early onset hereditary neuropathy with liability to pressure palsy. Issue 6 (30th October 2014)

5. Efficacy and safety of abobotulinumtoxinA liquid formulation in cervical dystonia: A randomized‐controlled trial. Issue 11 (21st September 2016)

6. Exome sequencing reveals mutations in MFN2 and GDAP1 in severe Charcot–Marie–Tooth disease. Issue 3 (September 2014)

7. Poster 155 Dysport®, AbobotulinumtoxinA, is Effective with a Favorable Safety Profile in the Treatment of Cervical Dystonia: A Phase III, Randomized, Double‐Blind, Placebo‐Controlled Study. Issue 9 (29th September 2014)