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2. A novel de novo point mutation of the OCT‐binding site in the IGF2/H19‐imprinting control region in a Beckwith–Wiedemann syndrome patient. (4th December 2013)

5. Agonistic anti‐human Fas monoclonal antibody induces fibroblast‐like synoviocyte apoptosis in haemophilic arthropathy: potential therapeutic implications. (20th November 2013)

6. Autosomal recessive cystinuria caused by genome‐wide paternal uniparental isodisomy in a patient with Beckwith–Wiedemann syndrome. (8th November 2014)

8. SAT0557 Diagnostic Performance of Rheumatoid Factor and Anti-CCP Antibody for Detecting Undiagnosed Rheumatoid Arthritis in Annual Health Check. (23rd January 2014)