P08.26 Venous thromboembolism and survival in patients with glioblastoma multiforme

od Rodenburg, R. J., Beerepoot, L. V.
Wydane w Neuro Oncol (2016)

P13.08 The validation of Melanoma GPA and Chowdhury overall survival score in patients with melanoma brain metastases treated with Gamma Knife surgery

od Rodenburg, R. J., Hanssens, P. E. J.
Wydane w Neuro Oncol (2016)

The liver-specific promoter of the human insulin-like growth factor II gene is activated by CCAAT/enhancer binding protein (C/EBP).

od van Dijk, M A, Rodenburg, R J, Holthuizen, P, Sussenbach, J S
Wydane 1992

Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1

od Balasubramaniam, S., Choy, Y. S., Talib, A., Norsiah, M. D., van den Heuvel, L. P., Rodenburg, R. J.
Wydane 2011

A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children

od Joost, K., Rodenburg, R.J., Piirsoo, A., van den Heuvel, L., Žordania, R., Põder, H., Talvik, I., Kilk, K., Soomets, U., Õunap, K.
Wydane 2012

Socio-emotional Problems in Children with CDG

od van de Loo, K. F. E., van Dongen, L., Mohamed, M., Gardeitchik, T., Kouwenberg, T. W., Wortmann, S. B., Rodenburg, R. J. T., Lefeber, D. J., Morava, E., Verhaak, C. M.
Wydane 2013

Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD)

od Balasubramaniam, Shanti, Lewis, B., Mock, D. M., Said, H. M., Tarailo-Graovac, M., Mattman, A., van Karnebeek, C. D., Thorburn, D. R., Rodenburg, R. J., Christodoulou, J.
Wydane w JIMD Rep (2016)

Skeletal muscle toxicity associated with tyrosine kinase inhibitor therapy in patients with chronic myeloid leukemia

od Janssen, L., Frambach, S. J. C. M., Allard, N. A. E., Hopman, M. T. E., Schirris, T. J. J., Voermans, N. C., Rodenburg, R. J., Blijlevens, N. M. A., Timmers, S.
Wydane w Leukemia (2019)

Disturbed energy metabolism and muscular dystrophy caused by pure creatine deficiency are reversible by creatine intake

od Nabuurs, C I, Choe, C U, Veltien, A, Kan, H E, van Loon, L J C, Rodenburg, R J T, Matschke, J, Wieringa, B, Kemp, G J, Isbrandt, D, Heerschap, A
Wydane 2013

Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions

od Renkema, G. H., Visser, G., Baertling, F., Wintjes, L. T., Wolters, V. M., van Montfrans, J., de Kort, G. A. P., Nikkels, P. G. J., van Hasselt, P. M., van der Crabben, S. N., Rodenburg, R. J. T.
Wydane w Hum Genet (2017)

Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

od Koene, S., Rodenburg, R. J., van der Knaap, M. S., Willemsen, M. A. A. P., Sperl, W., Laugel, V., Ostergaard, E., Tarnopolsky, M., Martin, M. A., Nesbitt, V., Fletcher, J., Edvardson, S., Procaccio, V., Slama, A., van den Heuvel, L. P. W. J., Smeitink, J. A. M.
Wydane 2012

A multi-center comparison of diagnostic methods for the biochemical evaluation of suspected mitochondrial disorders

od Rodenburg, R.J.T., Schoonderwoerd, G.C., Tiranti, V., Taylor, R.W., Rötig, A., Valente, L., Invernizzi, F., Chretien, D., He, L., Backx, G.P.B.M., Janssen, K.J.G.M., Chinnery, P.F., Smeets, H.J., de Coo, I.F., van den Heuvel, L.P.
Wydane 2013

Genotype-specific abnormalities in mitochondrial function associate with distinct profiles of energy metabolism and catecholamine content in pheochromocytoma and paraganglioma

od Rao, J.U., Engelke, U.F.H., Rodenburg, R.J.T., Wevers, R.A., Pacak, K., Eisenhofer, G., Qin, N., Kusters, B., Goudswaard, A.G., Lenders, J.W.M, Hermus, A.R.M.M., Mensenkamp, A.R., Kunst, H.P.M., Sweep, F.C.G.J., Timmers, H.J.L.M.
Wydane 2013