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Published in American journal of neuroradiology : AJNR (01.04.2004)
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Published in American journal of neuroradiology : AJNR (01.04.2004)
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The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients
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Biochemical hallmarks of tyrosine hydroxylase deficiency
Brautigam, Christa, Wevers, Ron A, Jansen, Riet J. T, Smeitink, Jan A. M, Andel, Johanneke F. de Rijk-van, Gabreels, Fons J. M, Hoffmann, Georg F
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Published in Clinical chemistry (Baltimore, Md.) (01.09.1998)
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Increased Cerebrospinal Fluid Glycine: A Biochemical Marker for a Leukoencephalopathy With Vanishing White Matter
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Published in Journal of child neurology (01.11.1999)
Published in Journal of child neurology (01.11.1999)
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A new motor performance test in a prospective study on children with suspected myopathy
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Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis
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Published in Brain (London, England : 1878) (01.05.2000)
Published in Brain (London, England : 1878) (01.05.2000)
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Spina bifida and parental occupation
Blatter, B M, Roeleveld, N, Zielhuis, G A, Mullaart, R A, Gabreëls, F J
Published in Epidemiology (Cambridge, Mass.) (01.03.1996)
Published in Epidemiology (Cambridge, Mass.) (01.03.1996)
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Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findings
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Published in Radiology (01.12.2000)
Published in Radiology (01.12.2000)
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Diagnosis and differential diagnosis of muscle cramps: a clinical approach
Jansen, Paul H P, Gabreëls, Fons J M, van Engelen, Baziel G M
Published in Journal of clinical neuromuscular disease (01.12.2002)
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A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome
de Vries, D D, van Engelen, B G, Gabreëls, F J, Ruitenbeek, W, van Oost, B A
Published in Annals of neurology (01.09.1993)
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Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy
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Molecular genetic analysis of human folate receptors in neural tube defects
Heil, S G, van der Put, N M, Trijbels, F J, Gabreëls, F J, Blom, H J
Published in European journal of human genetics : EJHG (01.04.1999)
Published in European journal of human genetics : EJHG (01.04.1999)
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