Identification of Pseudomonas aeruginosa and Aspergillus fumigatus mono- and co-cultures based on volatile biomarker combinations
Neerincx, A H, Geurts, B P, Habets, M F J, Booij, J A, van Loon, J, Jansen, J J, Buydens, L M C, van Ingen, J, Mouton, J W, Harren, F J M, Wevers, R A, Merkus, P J F M, Cristescu, S M, Kluijtmans, L A J
Published in Journal of breath research (29.01.2016)
Published in Journal of breath research (29.01.2016)
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3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathy
Wortmann, S B, Kremer, B H, Graham, A, Willemsen, M A, Loupatty, F J, Hogg, S L, Engelke, U F, Kluijtmans, L A, Wanders, R J, Illsinger, S, Wilcken, B, Cruysberg, J R, Das, A M, Morava, E, Wevers, R A
Published in Neurology (21.09.2010)
Published in Neurology (21.09.2010)
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Alcohol increases homocysteine and reduces B vitamin concentration in healthy male volunteers—a randomized, crossover intervention study
Gibson, A., Woodside, J.V., Young, I.S., Sharpe, P.C., Mercer, C., Patterson, C.C., Mckinley, M.C., Kluijtmans, L.A.J., Whitehead, A.S., Evans, A.
Published in QJM : An International Journal of Medicine (01.11.2008)
Published in QJM : An International Journal of Medicine (01.11.2008)
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P-glycoprotein-deficient mice have proximal tubule dysfunction but are protected against ischemic renal injury
Huls, M., Kramers, C., Levtchenko, E.N., Wilmer, M.J.G., Dijkman, H.B.P.M., Kluijtmans, L.A.J., van der Hoorn, J.W.A., Russel, F.G.M., Masereeuw, R.
Published in Kidney international (01.11.2007)
Published in Kidney international (01.11.2007)
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Journal Article
Cerebrotendinous xanthomatosis without neurological involvement
Stelten, B. M. L., Raal, F. J., Marais, A. D., Riksen, N. P., Roeters van Lennep, J. E., Duell, P.B, Graaf, M., Kluijtmans, L. A. J., Wevers, R. A., Verrips, A.
Published in Journal of internal medicine (01.11.2021)
Published in Journal of internal medicine (01.11.2021)
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Journal Article
Detection of Staphylococcus aureus in cystic fibrosis patients using breath VOC profiles
Neerincx, A H, Geurts, B P, van Loon, J, Tiemes, V, Jansen, J J, Harren, F J M, Kluijtmans, L A J, Merkus, P J F M, Cristescu, S M, Buydens, L M C, Wevers, R A
Published in Journal of breath research (30.11.2016)
Published in Journal of breath research (30.11.2016)
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Journal Article
Fever‐induced recurrent rhabdomyolysis due to a novel mutation in the ryanodine receptor type 1 gene
Molenaar, J. P., Voermans, N. C., Hoeve, B. J., Kamsteeg, E. J., Kluijtmans, L. A., Kusters, B., Jungbluth, H. J., Engelen, B. G.
Published in Internal medicine journal (01.08.2014)
Published in Internal medicine journal (01.08.2014)
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Early molecular events in the development of the diabetic cardiomyopathy
Mönkemann, H, De Vriese, A S, Blom, H J, Kluijtmans, L A J, Heil, S G, Schild, H H, Golubnitschaja, O
Published in Amino acids (01.01.2002)
Published in Amino acids (01.01.2002)
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The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency
Voermans, N.C., Poels, P.J., Kluijtmans, L.A., Engelen, B.G.van
Published in Neuromuscular disorders : NMD (01.12.2005)
Published in Neuromuscular disorders : NMD (01.12.2005)
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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase
Frosst, P, Blom, H.J, Milos, R, Goyette, P, Sheppard, C.A, Matthews, R.G, Boers, G.J.H, den Heijer, M, Kluijtmans, L.A.J, van den Heuve, L.P, Rozen, R
Published in Nature genetics (01.05.1995)
Published in Nature genetics (01.05.1995)
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Journal Article
Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
Kluijtmans, L A, van den Heuvel, L P, Boers, G H, Frosst, P, Stevens, E M, van Oost, B A, den Heijer, M, Trijbels, F J, Rozen, R, Blom, H J
Published in American journal of human genetics (01.01.1996)
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Published in American journal of human genetics (01.01.1996)
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Clinical imaging and neuropathological correlations in an unusual case of cerebrotendinous xanthomatosis
Wallon, D, Guyant-Maréchal, L, Laquerrière, A, Wevers, R A, Martinaud, O, Kluijtmans, L A J, Yntema, H G, Saugier-Veber, P, Hannequin, D
Published in Clinical neuropathology (01.11.2010)
Published in Clinical neuropathology (01.11.2010)
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The Molecular Basis of Cystathionine β-Synthase Deficiency in Dutch Patients with Homocystinuria: Effect of CBS Genotype on Biochemical and Clinical Phenotype and on Response to Treatment
Kluijtmans, Leo A.J., Boers, Godfried H.J., Kraus, Jan P., van den Heuvel, Lambert P. W.J., Cruysberg, Johan R.M., Trijbels, Frans J.M., Blom, Henk J.
Published in American journal of human genetics (01.07.1999)
Published in American journal of human genetics (01.07.1999)
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Journal Article
The 677C→T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease
Verhoef, Petra, Kok, Frans J, Kluijtmans, Leo A.J, Blom, Henk J, Refsum, Helga, Ueland, Per M, Kruyssen, Dick A.C.M
Published in Atherosclerosis (11.07.1997)
Published in Atherosclerosis (11.07.1997)
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Journal Article
Sequence analysis of the coding region of human methionine synthase : relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease
VAN DER PUT, N. M. J, VAN DER MOLEN, E. F, KLUIJTMANS, L. A. J, HEIL, S. G, TRIJBELS, J. M. F, ESKES, T. K. A. B, VAN OPPENRAAIJ-EMMERZAAL, D, BANERJEE, R, BLOM, H. J
Published in QJM : An International Journal of Medicine (01.08.1997)
Published in QJM : An International Journal of Medicine (01.08.1997)
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The 894 G > T variant of endothelial nitric oxide synthase (eNOS) increases the risk of recurrent venous thrombosis through interaction with elevated homocysteine levels
Heil, S. G., Den Heijer, M., Van Der Rijt‐Pisa, B. J. M., Kluijtmans, L. A. J., Blom, H. J.
Published in Journal of thrombosis and haemostasis (01.05.2004)
Published in Journal of thrombosis and haemostasis (01.05.2004)
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