Literature DB >> 8701425

Purpura fulminans in a patient homozygous for a mutation in the protein C gene--prenatal diagnosis in a subsequent pregnancy.

M C Alessi, M F Aillaud, O Paut, B Roquelaure, M Alhenc-Gelas, M C Pellissier, N Ghanen, I Juhan-Vague.   

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Year:  1996        PMID： 8701425

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN： 0340-6245            Impact factor:   5.249


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  2 in total

Review 1.  Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism.

Authors:  U Nowak-Göttl; K Auberger; U Göbel; W Kreuz; R Schneppenheim; H Vielhaber; W Zenz; B Zieger
Journal:  Eur J Pediatr       Date:  1996-11       Impact factor: 3.183

2.  Prenatal genetic testing for familial severe congenital protein C deficiency.

Authors:  Shinya Tairaku; Mariko Taniguchi-Ikeda; Yoko Okazaki; Yoriko Noguchi; Yuji Nakamachi; Takeshi Mori; Ikuko Kubokawa; Akira Hayakawa; Akio Shibata; Tomomi Emoto; Hiroki Kurahashi; Tatsushi Toda; Seiji Kawano; Hideto Yamada; Ichiro Morioka; Kazumoto Iijima
Journal:  Hum Genome Var       Date:  2015-06-25
  2 in total

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