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1. Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study. Issue 3 (30th July 2017)

2. Clinical and genetic features of Charcot‐Marie‐Tooth disease 2F and hereditary motor neuropathy 2B in Japan. Issue 1 (14th February 2018)

3. Clinical features of inherited neuropathy with BSCL2 mutations in Japan. Issue 2 (12th March 2020)

5. Genetic profile and onset features of 1005 patients with Charcot-Marie-Tooth disease in Japan. Issue 2 (26th September 2018)

6. Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan. Issue 3 (27th November 2020)

7. Hypercapnia versus normocapnia for emergence from desflurane anaesthesia: Single-blinded randomised controlled study. Issue 11 (November 2021)

8. Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-syndromic Hearing Loss. Issue 7 (August 2021)