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

Tekijä Rodenburg, R. J., Beerepoot, L. V.
Julkaisussa 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

Tekijä Rodenburg, R. J., Hanssens, P. E. J.
Julkaisussa 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).

Tekijä van Dijk, M A, Rodenburg, R J, Holthuizen, P, Sussenbach, J S
Julkaistu 1992

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

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

A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children

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

Socio-emotional Problems in Children with CDG

Tekijä 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.
Julkaistu 2013

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

Tekijä 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.
Julkaisussa JIMD Rep (2016)

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

Tekijä 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.
Julkaisussa Leukemia (2019)

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

Tekijä 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
Julkaistu 2013

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

Tekijä 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.
Julkaisussa 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

Tekijä 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.
Julkaistu 2012

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

Tekijä 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.
Julkaistu 2013

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

Tekijä 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.
Julkaistu 2013