Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene

Por van Rij, Maartje C., Jansen, Fenna A. R., Hellebrekers, Debby M. E. I., Onkenhout, W., Smeets, Hubert J. M., Hendrickx, Alexandra T., Gottschalk, Ralph W. H., Steggerda, Sylke J., Peeters‐Scholte, Cacha M. P. C. D., Haak, Monique C., Hilhorst‐Hofstee, Yvonne
Publicado no Clin Case Rep (2016)

Midtrimester preterm prelabour rupture of membranes (PPROM): expectant management or amnioinfusion for improving perinatal outcomes (PPROMEXIL – III trial)

Por van Teeffelen, Augustinus S P, van der Ham, David P, Willekes, Christine, Al Nasiry, Salwan, Nijhuis, Jan G, van Kuijk, Sander, Schuyt, Ewoud, Mulder, Twan L M, Franssen, Maureen T M, Oepkes, Dick, Jansen, Fenna A R, Woiski, Mallory D, Bekker, Mireille N, Bax, Caroline J, Porath, Martina M, de Laat, Monique W M, Mol, Ben W, Pajkrt, Eva
Publicado em 2014