T cells from baxalpha transgenic mice show accelerated apoptosis in response to stimuli but do not show restored DNA damage-induced cell death in the absence of p53.

Por Brady, H J, Salomons, G S, Bobeldijk, R C, Berns, A J
Publicado em 1996

Efficacy of Vigabatrin Intervention in a Mild Phenotypic Expression of Succinic Semialdehyde Dehydrogenase Deficiency

Por Casarano, M., Alessandrì, M G., Salomons, G. S., Moretti, E., Jakobs, C., Gibson, K. M., Cioni, G., Battini, R.
Publicado em 2011

Pyridoxine responsive epilepsy caused by a novel homozygous PNPO mutation()

Por Jaeger, B., Abeling, N.G., Salomons, G.S., Struys, E.A., Simas-Mendes, M., Geukers, V.G., Poll-The, B.T.
Publicado no Mol Genet Metab Rep (2016)

X-linked creatine transporter defect: A report on two unrelated boys with a severe clinical phenotype

Por Anselm, I. M., Alkuraya, F. S., Salomons, G. S., Jakobs, C., Fulton, A. B., Mazumdar, M., Rivkin, M., Frye, R., Poussaint, T. Young, Marsden, D.
Publicado em 2006

Targeted screening of succinic semialdehyde dehydrogenase deficiency (SSADHD) employing an enzymatic assay for γ-hydroxybutyric acid (GHB) in biofluids

Por Wernli, C., Finochiaro, S., Volken, C., Andresen-Streichert, H., Buettler, A., Gygax, D., Salomons, G.S., Jansen, E.E., Ainslie, G.R., Vogel, K.R., Gibson, K.M.
Publicado no Mol Genet Metab Rep (2016)