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No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.

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Title: No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
Authors: Miyata T; Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, 5-7-1 Fujishirodai, Suita, Osaka, 565-8565, Japan. miyata@ncvc.go.jp., Uchida Y; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan., Yoshida Y; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan., Kato H; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan., Matsumoto M; Department of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan., Kokame K; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan., Fujimura Y; Japanese Red Cross Kinki Blood Center, Ibaraki, Japan., Nangaku M; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan.
Source: International journal of hematology [Int J Hematol] 2016 Aug; Vol. 104 (2), pp. 223-7. Date of Electronic Publication: 2016 May 18.
Publication Type: Journal Article
Journal Info: Publisher: Springer Japan Country of Publication: Japan NLM ID: 9111627 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1865-3774 (Electronic) Linking ISSN: 09255710 NLM ISO Abbreviation: Int J Hematol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
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  Data: <searchLink fieldCode="AU" term="%22Miyata+T%22">Miyata T</searchLink>; Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, 5-7-1 Fujishirodai, Suita, Osaka, 565-8565, Japan. miyata@ncvc.go.jp.<br /><searchLink fieldCode="AU" term="%22Uchida+Y%22">Uchida Y</searchLink>; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan.<br /><searchLink fieldCode="AU" term="%22Yoshida+Y%22">Yoshida Y</searchLink>; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan.<br /><searchLink fieldCode="AU" term="%22Kato+H%22">Kato H</searchLink>; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan.<br /><searchLink fieldCode="AU" term="%22Matsumoto+M%22">Matsumoto M</searchLink>; Department of Blood Transfusion Medicine, Nara Medical University, Kashihara, Japan.<br /><searchLink fieldCode="AU" term="%22Kokame+K%22">Kokame K</searchLink>; Department of Molecular Pathogenesis, National Cerebral and Cardiovascular Center, Suita, Japan.<br /><searchLink fieldCode="AU" term="%22Fujimura+Y%22">Fujimura Y</searchLink>; Japanese Red Cross Kinki Blood Center, Ibaraki, Japan.<br /><searchLink fieldCode="AU" term="%22Nangaku+M%22">Nangaku M</searchLink>; Division of Nephrology and Endocrinology, University of Tokyo School of Medicine, Tokyo, Japan.
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  Data: <searchLink fieldCode="JN" term="%229111627%22">International journal of hematology</searchLink> [Int J Hematol] 2016 Aug; Vol. 104 (2), pp. 223-7. <i>Date of Electronic Publication: </i>2016 May 18.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer+Japan%22">Springer Japan </searchLink><i>Country of Publication: </i>Japan <i>NLM ID: </i>9111627 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1865-3774 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209255710%22">09255710 </searchLink><i>NLM ISO Abbreviation: </i>Int J Hematol <i>Subsets: </i>MEDLINE
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        Value: 10.1007/s12185-016-2021-3
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        Text: English
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      – TitleFull: No association between dysplasminogenemia with p.Ala620Thr mutation and atypical hemolytic uremic syndrome.
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              Text: 2016 Aug
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