P. Eskes

发表

Rhabdomyolysis in early-onset very long-chain acyl-CoA dehydrogenase deficiency despite normal glucose after fasting

L. Dorland, G. Visser, H. Engbers, 2005, Journal of Inherited Metabolic Disease.

Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation: clinical, biochemical and DNA analyses in a four-generation family.

M. Durán, E. Bakker, B. Poll-The, 1997, American journal of medical genetics.

Lower versus Traditional Treatment Threshold for Neonatal Hypoglycemia.

J. H. van der Lee, L. Zimmermann, B. Semmekrot, 2020, The New England journal of medicine.

[Severe vitamin-D deficiency in more than half of the immigrant pregnant women of non-western origin and their newborns].

J. Wielders, P. Eskes, M. Duk, 2006, Nederlands tijdschrift voor geneeskunde.