Genetic variations in complement factors in patients with congenital thrombotic thrombocytopenic purpura with renal insufficiency

International Journal of Hematology

Volumn 103, Issue 3, 2016, Pages 283-291

  Fan, Xinping ^a,f   Kremer Hovinga, Johanna A ^b   Shirotani Ikejima, Hiroko ^a   Eura, Yuka ^a   Hirai, Hidenori ^a   Honda, Shigenori ^a   Kokame, Koichi ^a   Taleghani, Magnus Mansouri ^b   von Krogh, Anne Sophie ^c,d   Yoshida, Yoko ^e   Fujimura, Yoshihiro ^e   Lämmle, Bernhard ^b,g   Miyata, Toshiyuki ^a  

^a NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

^b UNIVERSITY OF BERN   (Switzerland)

^c NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^d TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

^e NARA MEDICAL UNIVERSITY   (Japan)

^f CAPITAL MEDICAL UNIVERSITY   (China)

^g UNIVERSITY MEDICAL CENTER MAINZ   (Germany)

Author keywords

Atypical hemolytic uremic syndrome; Complement factors; Renal insufficiency; Thrombotic thrombocytopenic purpura; Upshaw Schulman syndrome

Indexed keywords

ALTERNATIVE COMPLEMENT PATHWAY C3 C5 CONVERTASE; COMPLEMENT COMPONENT C3; COMPLEMENT FACTOR; COMPLEMENT FACTOR H; COMPLEMENT FACTOR I; MEMBRANE COFACTOR PROTEIN; THROMBOMODULIN; VON WILLEBRAND FACTOR CLEAVING PROTEINASE; ADAMTS13 PROTEIN, HUMAN;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; EUROPEAN; FEMALE; GENE DELETION; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; GENOMICS; HEMOLYTIC UREMIC SYNDROME; HUMAN; JAPANESE (PEOPLE); KIDNEY FAILURE; MALE; MIDDLE AGED; MISSENSE MUTATION; POLYMERASE CHAIN REACTION; QUANTITATIVE ANALYSIS; SEVERE RENAL IMPAIRMENT; THROMBOTIC THROMBOCYTOPENIC PURPURA; GENETIC ASSOCIATION STUDY; GENETICS; PURPURA, THROMBOTIC THROMBOCYTOPENIC; RENAL INSUFFICIENCY;

ADAMTS13 PROTEIN; ADULT; ATYPICAL HEMOLYTIC UREMIC SYNDROME; COMPLEMENT C3; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; PURPURA, THROMBOTIC THROMBOCYTOPENIC; RENAL INSUFFICIENCY;

EID: 84959575823     PISSN: 09255710     EISSN: 18653774     Source Type: Journal    
DOI: 10.1007/s12185-015-1933-7     Document Type: Article

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