F. M. Vaz

Prolonged moderate-intensity exercise without and with L-carnitine supplementation in patients with MCAD deficiency (2006)

Huidekoper, H.H., Schneider, J., Westphal, T., Vaz, F.M., Duran, M., Wijburg, F.A.

Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is probably the most common inborn error of fatty acid oxidation (FAO). Routine L-carnitine supplementation in the treatment of MCADD is...

Measurement of carnitine biosynthesis enzyme activities by tandem mass spectrometry: Differences between the mouse and the rat (2006)

Vlies, N. Van, Wanders, R.J.A., Vaz, F.M.

L-carnitine is synthesized in the human fetal-placental unit: Potential roles in placental and fetal metabolism (2006)

Oey, N.A., Vlies, N. Van, Wijburg, F.A., Wanders, R.J.A., Attié-Bitach, T., Vaz, F.M.

Identification and characterization of human cardiolipin synthase (2006)

Houtkooper, R.H., Akbari, H., Lenthe, H. Van, Kulik, W., Wanders, R.J.A., Frentzen, M., ...

Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse (2005)

Vlies, N. Van, Tian, L., Overmars, H., Bootsma, A.H., Kulik, W., Wanders, R.J.A., ...

Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis (2005)

Valianpour, F., Mitsakos, V., Schlemmer, D., Towbin, J.A., Taylor, J.M., Ekert, P.G., ...

Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice (2005)

Spiekerkoetter, U., Tokunaga, C., Wendel, U., Mayatepek, E., Ijlst, L., Vaz, F.M., ...

Functional analysis of TMLH variants and definition of domains required for catalytic activity and mitochondrial targeting (2005)

Monfregola, J., Cevenini, A., Terracciano, A., Vlies, N. Van, Arbucci, S., Wanders, R.J.A., ...

A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARalpha-dependent and -independent pathways (2005)

Gloerich, J., Vlies, N. Van, Jansen, G.A., Dennis, S., Ruiter, J.P.N., Werkhoven, M.A. Van, ...

The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome (2004)

Ma, L., Vaz, F.M., Gu, Z., Wanders, R.J.A., Greenberg, M.L.

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update (2004)

Barth, P.G., Valianpour, F., Bowen, V.M., Lam, J., Duran, M., Vaz, F.M., ...

Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome (2004)

Gu, Z., Valianpour, F., Chen, S., Vaz, F.M., Hakkaart, G.A.J., Wanders, R.J.A., ...

Only one splice variant of the human TAZ gene encodes a functional protein with a role in cardiolipin metabolism (2003)

Vaz, F.M., Houtkooper, R.H., Valianpour, F., Barth, P.G., Wanders, R.J.A.

Linoleic acid supplemention of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatment (2003)

Valianpour, F., Wanders, R.J.A., Overmars, H., Vaz, F.M., Barth, P.G., Gennip, A.H. Van

Molecular and biochemical aspects of carnitine biosynthesis (2002)

Vaz, F.M.

Carnitine biosynthesis in Neurospora crassa: identification of a cDNA coding for epsilon-N-trimethyllysine hydroxylase and its functional expression in Saccharomyces cerevisiae (2002)

Swiegers, J.H., Vaz, F.M., Pretorius, I.S., Wanders, R.J.A., Bauer, F.F.

Carnitine biosynthesis in mammals [review article] (2002)

Vaz, F.M., Wanders, R.J.A.

Identification of two novel mutations in OCTN2 from two Saudi patients with systemic carnitine deficiency (2002)

Rahbeeni, Z., Vaz, F.M., Al-Hussein, K., Bucknall, M.P., Ruiter, J., Wanders, R.J.A., ...

Analysis of carnitine biosynthesis metabolites in urine by HPLC-electrospray tandem mass spectrometry (2002)

Vaz, F.M., Melegh, B., Bene, J., Cuebas, D., Gage, D.A., Bootsma, A., ...

Molecular and biochemical characterization of rat epsilon-N-Trimethyllysine hydroxylase, the first enzyme of carnitine (2001)

Vaz, F.M., Ofman, R., Westinga, K., Back, J.W., Wanders, R.J.A.

Molecular and biochemical characterization of rat epsilon-N-Trimethyllysine hydroxylase, the first enzyme of carnitine (2001)

Vaz, F.M., Ofman, R., Westinga, K., Back, J.W., Wanders, R.J.A.

Molecular and biochemical characterization of rat gamma-trimethylaminobutyraldehyde dehydrogenase and evidence for the involvement of human aldehyde dehydrogenase 9 in carnitine biosynthesis (2000)

Vaz, F.M., Fouchier, S.W., Ofman, R., Sommer, M., Wanders, R.J.A.

Carnitine biosynthesis: purification of gamma-butyrobetaine hydroxylase from rat liver (1999)

Vaz, F.M., Gool, S. Van, Ofman, R., Ijlst, L., Wanders, R.J.A.

Identification of two novel mutations in OCTN2 of three patients with systemic carcitine deficiency (1999)

Vaz, F.M., Scholte, H.R., Ruiter, J., Hussaarts-Odijk, L.M., Rodrigues Pereira, R., Schweitzer, S., ...

Carnitine biosynthesis: identification of the cDNA encoding human gamma-butyrobetaine hydroxylase (1998)

Vaz, F.M., Gool, S.W. Van, Ofman, R., Ijlst, L., Wanders, R.J.A.