Use of rifampin in persistent coagulase negative staphylococcal bacteremia in neonates

Por van der Lugt, N Margreth, Steggerda, Sylke J, Walther, Frans J
Publicado em 2010

Thrombocytopenia in neonatal sepsis: Incidence, severity and risk factors

Por Ree, Isabelle M. C., Fustolo-Gunnink, Suzanne F., Bekker, Vincent, Fijnvandraat, Karin J., Steggerda, Sylke J., Lopriore, Enrico
Publicado no PLoS One (2017)

Late-onset sepsis due to urinary tract infection in very preterm neonates is not uncommon

Por Mohseny, Alexander B., van Velze, Veerle, Steggerda, Sylke J., Smits-Wintjens, Vivianne E. H. J., Bekker, Vincent, Lopriore, Enrico
Publicado no Eur J Pediatr (2017)

Is sequential cranial ultrasound reliable for detection of white matter injury in very preterm infants?

Por Leijser, Lara M., de Bruïne, Francisca T., van der Grond, Jeroen, Steggerda, Sylke J., Walther, Frans J., van Wezel-Meijler, Gerda
Publicado em 2010

Neonatal Thrombocytopenia after Perinatal Asphyxia Treated with Hypothermia: A Retrospective Case Control Study

Por Boutaybi, N., Razenberg, F., Smits-Wintjens, V. E. H. J., van Zwet, E. W., Rijken, M., Steggerda, S. J., Lopriore, E.
Publicado em 2014

Posterior fossa abnormalities in high-risk term infants: comparison of ultrasound and MRI

Por Steggerda, S. J., de Bruïne, F. T., Smits-Wintjens, V. E. H. J., Verbon, P., Walther, F. J., van Wezel-Meijler, G.
Publicado no Eur Radiol (2015)

Successful treatment of fetal hemolytic disease due to glucose phosphate isomerase deficiency (GPI) using repeated intrauterine transfusions: a case report

Por Adama van Scheltema, Phebe N, Zhang, Ai, Ball, Lynne M, Steggerda, Sylke J, van Wijk, Richard, Fransen van de Putte, Dietje E, van Kamp, Inge L
Publicado no Clin Case Rep (2015)

Cerebral imaging and neurodevelopmental outcome after entero- and human parechovirus sepsis in young infants

Por de Jong, Eveline P., Holscher, Herma C., Steggerda, Sylke J., Van Klink, Jeanine M. M., van Elzakker, Erika P. M., Lopriore, Enrico, Walther, Frans J., Brus, Frank
Publicado no Eur J Pediatr (2017)

Congenital disorder of glycosylation type Ia presenting with hydrops fetalis

Por van de Kamp, J M, Lefeber, D J, Ruijter, G J G, Steggerda, S J, den Hollander, N S, Willems, S M, Matthijs, G, Poorthuis, B J H M, Wevers, R A
Publicado em 2007

Bloodstream Infection Incidence of Different Central Venous Catheters in Neonates: A Descriptive Cohort Study

Por Dubbink-Verheij, Gerdina H., Bekker, Vincent, Pelsma, Iris C. M., van Zwet, Erik W., Smits-Wintjens, Vivianne E. H. J., Steggerda, Sylke J., te Pas, Arjan B., Lopriore, Enrico
Publicado no Front Pediatr (2017)

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)