HuGE Literature Finder
Rare Disease
Records 1-6
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F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency. Results from a genotype-phenotype study.
Thrombosis and haemostasis 2017 Apr . Quintavalle Gabriele, Riccardi Federica, Rivolta Gianna Franca, Martorana Davide, Di Perna Caterina, Percesepe Antonio, Tagliaferri Annarita, |
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[Mutation analysis and prenatal diagnosis for a family affected with congenital factor VII deficiency].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2016 Jun 33 (3): 357-60. Peng Wei, Zhang Shuxin, Liu Xin, Gu Yanan, Wang Y |
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Isotypic analysis of antibodies against activated Factor VII in patients with Factor VII deficiency using the x-MAP technology.
Thrombosis research 2016 Feb 141 22-27. Pfeiffer Caroline, Mathieu-Dupas Eve, Logghe Pauline, Lissalde-Lavigne Géraldine, Balicchi Julien, Caliskan Umran, Valentin Thomas, Laune Daniel, Molina Franck, Schved Jean François, Giansily-Blaizot Muri |
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Long-term prophylaxis in severe factor VII deficiency.
Haemophilia : the official journal of the World Federation of Hemophilia 2015 May . Siboni S M, Biguzzi E, Mistretta C, Garagiola I, Peyvandi |
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Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.
Haemophilia : the official journal of the World Federation of Hemophilia 2009 Jan 15 (1): 267-80. Herrmann F H, Wulff K, Auerswald G, Schulman S, Astermark J, Batorova A, Kreuz W, Pollmann H, Ruiz-Saez A, De Bosch N, Salazar-Sanchez L, |
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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.
Thrombosis and haemostasis 2005 Mar 93 (3): 481-7. Mariani Guglielmo, Herrmann Falko H, Dolce Alberto, Batorova Angelika, Etro Daniela, Peyvandi Flora, Wulff Karin, Schved Jean F, Auerswald Günter, Ingerslev Jorgen, Bernardi Francesco, |
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- Page last updated:Sep 22, 2021
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