Gerry C. H. Steenbergen‐Spanjers

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

Michèl A.A.P. Willemsen, Marcel M. Verbeek, Erik‐Jan Kamsteeg et al. · Brain · 2010 · 228 citations · Full text

Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia

Georg F. Hoffmann, Birgit Assmann, Christa Br�utigam et al. · Annals of Neurology · 2003 · 129 citations

A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

Lambert P.W.J. van den Heuvel, Bernadette Luiten, J.F. de Rijk-van Andel et al. · Human Genetics · 1998 · 109 citations

Tyrosine Hydroxylase Gene, Mendelian Disorder, Genetic Disorder +5

Tyrosine hydroxylase deficiency: Clinical manifestations of catecholamine insufficiency in infancy

Padraic J. Grattan‐Smith, Ron A. Wevers, Gerry C. H. Steenbergen‐Spanjers et al. · Movement Disorders · 2002 · 70 citations

Biochemical and Molecular Genetic Characteristics of the Severe Form of Tyrosine Hydroxylase Deficiency

Christa Bräutigam, Gerry C. H. Steenbergen‐Spanjers, Georg F. Hoffmann et al. · Clinical Chemistry · 1999 · 57 citations · Full text