A Dutch family with moderately severe hemophilia B (factor IXHeerde) has a missense mutation identical to that of factor IX London 2.

Por Poort, S R, Briët, E, Bertina, R M, Reitsma, P H
Publicado em 1989

A Dutch pedigree with mild hemophilia B with a missense mutation in the first EGF domain (factor IXOud en Nieuw Gastel).

Por Poort, S R, Briët, E, Bertina, R M, Reitsma, P H
Publicado em 1989

Modification of the N-terminus of human factor IX by defective propeptide cleavage or acetylation results in a destabilized calcium-induced conformation: effects on phospholipid bi...

Por Wojcik, E G, Van Den Berg, M, Poort, S R, Bertina, R M
Publicado em 1997

Factor IX Zutphen: a Cys18-->Arg mutation results in formation of a heterodimer with alpha 1-microglobulin and the inability to form a calcium-induced conformation.

Por Wojcik, E G, van den Berg, M, van der Linden, I K, Poort, S R, Cupers, R, Bertina, R M
Publicado em 1995

Fulminant meningococcal septic shock in a boy with combined inherited properdin and protein C deficiency.

Por Fijen, C A, Derkx, B H, Kuijper, E J, Mannens, M, Poort, S R, Peters, M, Daha, M R, Dankert, J
Publicado em 1995

MUC1 (EMA) is preferentially expressed by ALK positive anaplastic large cell lymphoma, in the normally glycosylated or only partly hypoglycosylated form

Por Ten, B, Snijdewint, F, von Mensdorff-Pou..., S, Poort-Keesom, R, Oudejans, J, Meijer, J, Willemze, R, Hilgers, J, Meijer, C
Publicado em 2001