Significance of screening for Fabry disease among male dialysis patients
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DOI[10.1007/s10157-005-0369-4]to the data of the same series
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- Material Type
- 記事
- Author/Editor
- Mayuri IchinoseMasaaki NakayamaToya Ohashi
- Publication, Distribution, etc.
- Publication Date
- 2005-09
- Publication Date (W3CDTF)
- 2005-09
- Periodical title
- Clinical and experimental nephrology : official publication of the Japanese Society of Nephrology
- No. or year of volume/issue
- 9(3)
- Volume
- 9(3)
- ISSN (Periodical Title)
- 1437-7799
- ISSN-L (Periodical Title)
- 1437-7799
- Text Language Code
- eng
- DOI
- 10.1007/s10157-005-0369-4
- Persistent ID (NDL)
- info:ndljp/pid/11493650
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2020-06-03T20:20:43+09:00
- Date Captured (W3CDTF)
- 2020-04-27
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11493643
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- DOI
- 10.1007/s10157-005-0369-4
- Related Material (URI)
- Is Referenced By
- Fabry disease: Biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitutionScreening of Male Dialysis Patients for Fabry Disease by Plasma GlobotriaosylsphingosineHigh-throughput screening identified disease-causing mutants and functional variants of α-galactosidase A gene in Japanese male hemodialysis patientsScreening of Fabry disease in patients with chronic kidney disease in Japanファブリー病透析患者における酵素補充療法の治療効果と,アガルシダーゼアルファの体内動態についてCase Reports : A Case of Fabry Disease, in Which Renal Symptoms Served as a Diagnostic PromptRenal variant of Fabry disease diagnosed by the presence of urinary mulberry cellsPathological Renal Findings of Chronic Renal Failure in a Patient with the E66Q Mutation in the α-galactosidase A GenePrevalence of Fabry disease in dialysis patients : Japan Fabry disease screening study (J-FAST)Role of the p.E66Q variant of GLA in the progression of chronic kidney disease
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossref
- Bibliographic ID (NDL)
- 11493650