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22. Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia. (5th September 2017)

23. CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis. (April 2017)

26. De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function. (November 2018)

29. EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia. Issue 3 (15th December 2020)

30. EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts. Issue 1 (3rd November 2014)