Author/Creator: Urata, Michiyo - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Urata, Michiyo

1. A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period. Issue 4 (20th September 2013)

Authors:: Unal, Sule; Gumruk, Fatma; Yigit, Sule; Tuncer, Murat; Tavil, Betul; Cil, Onur; Takci, Sahin; Urata, Michiyo; Hotta, Taeko; Kang, Dongchon; Cetin, Mualla
Journal:: Pediatric blood & cancer
Issue:: Volume 61:Issue 4(2014:Apr.)
Page Start:: 763
Record Type:: Journal Article
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2. The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene. Issue 7 (23rd January 2017)

Authors:: Inoue, Hirofumi; Terachi, Shin‐ichi; Uchiumi, Takeshi; Sato, Tetsuji; Urata, Michiyo; Ishimura, Masataka; Koga, Yui; Hotta, Taeko; Hara, Toshiro; Kang, Dongchon; Ohga, Shouichi
Journal:: Pediatric blood & cancer
Issue:: Volume 64:Issue 7(2017)
Page Start:: n/a
Record Type:: Journal Article
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3. Toxic myopathy with multiple deletions in mitochondrial DNA associated with long‐term use of oral anti‐viral drugs for hepatitis B: A case study. Issue 2 (7th March 2019)

Authors:: Fujii, Takayuki; Takase, Kei‐ichiro; Honda, Hiroyuki; Kawamura, Nobutoshi; Yamasaki, Ryo; Urata, Michiyo; Uchiumi, Takeshi; Iwaki, Toru; Kira, Jun‐ichi
Journal:: Neuropathology
Issue:: Volume 39:Issue 2(2019)
Page Start:: 162
Record Type:: Journal Article
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