Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may

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syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

An inherited bleeding disorder caused by the reduction in activity and antigen levels of both factor V and factor VIII with manifestation of mild-to-moderate bleeding symptoms. Caused by mutations either in the LMAN1 gene (chromosome 18; q21) or in t

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déficit combiné en facteurs V et VIII

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Von Willebrand factor | factor VIII:R

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facteur Willebrand | facteur VIII : R Ag | antigène Willebrand | cofacteur de la ristocétine

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

Deficiency factor VIII (with functional defect) Haemophilia:NOS | A | classical

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Carence en facteur VIII (avec anomalie fonctionnelle) Hémophilie:SAI | A | classique

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

erythropoietin | recombinant erythropoietin | renal erythropoietin factor | hemopoietin

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

érythropoïétine | EPO | hémopoïétine

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

D'autres ont cherché : recombinant human factor viii von willebrand factor antihemophilic factor classical erythropoietin factor viii hemopoietin rf viii recombinant erythropoietin recombinant factor viii renal erythropoietin factor recombinant factor VIII

datacenter (1): www.wordscope.fr (v4.0.br)

'recombinant factor VIII' ->

Date index: 2022-02-10