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1. Fulminant bilateral cerebral infarction caused by paradoxical embolism in a patient with protein S Ala525Val substitution. Issue 3 (9th January 2015)

2. Gene analysis of six cases of congenital protein S deficiency and functional analysis of protein S mutations (A139V, C449F, R451Q, C475F, A525V and D599TfsTer13). Issue 151 (March 2017)

3. Late onset thrombosis in two Japanese patients with compound heterozygote protein S deficiency. Issue 6 (June 2015)