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

Por Rodenburg, R. J., Beerepoot, L. V.
Publicado no 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

Por Rodenburg, R. J., Hanssens, P. E. J.
Publicado no 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).

Por van Dijk, M A, Rodenburg, R J, Holthuizen, P, Sussenbach, J S
Publicado em 1992

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

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

A simple and versatile method for frequent 24 h blood sample collection in healthy older adults

Por Akintola, A.A., Jansen, S.W., Wilde, R.B.P., Hultzer, G., Rodenburg, R., van Heemst, D.
Publicado no MethodsX (2014)

Superinduction of interleukin 8 mRNA in activated monocyte derived macrophages from rheumatoid arthritis patients

Por Rodenburg, R., van den Hoogen, F. H J, Barrera, P., van Venrooij, W. J, van de Putte, L. B A
Publicado em 1999

A Diagnostic Algorithm for Mitochondrial Disorders in Estonian Children

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

Socio-emotional Problems in Children with CDG

Por 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.
Publicado em 2013

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

Por 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.
Publicado no JIMD Rep (2016)

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

Por 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
Publicado em 2013

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

Por 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.
Publicado no 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

Por 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.
Publicado em 2012

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

Por 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.
Publicado em 2013

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

Por 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.
Publicado em 2013