Pathobiochemical implications of hyperdopaminuria in patients with aromatic L-amino acid decarboxylase deficiency

[1]  H. Levy Increasing brain tyrosine in treated phenylketonuria , 1998, Journal of Inherited Metabolic Disease.

[2]  S. Kaufman Some facts relevant to a consideration of a possible alternative treatment for classical phenylketonuria , 1998, Journal of Inherited Metabolic Disease.

[3]  P. Barth,et al.  Aromatic L-amino acid decarboxylase deficiency: A new case with a mild clinical presentation and unexpected laboratory findings , 1998, Journal of Inherited Metabolic Disease.

[4]  S. Milstien,et al.  Aromatic L-Amino Acid Decarboxylase Deficiency: Clinical Features, Diagnosis, and Treatment of a Second Family , 1997, Journal of child neurology.

[5]  T. Joh,et al.  Alternate Promoters in the Rat Aromatic l‐Amino Acid Decarboxylase Gene for Neuronal and Nonneuronal Expression: An In Situ Hybridization Study , 1996, Journal of neurochemistry.

[6]  J. Imbs,et al.  Renal dopamine excretion in healthy volunteers after oral ingestion of l‐Dopa , 1993, Fundamental & clinical pharmacology.

[7]  R. Surtees,et al.  Aromatic L‐amino acid decarboxylase deficiency , 1992, Neurology.

[8]  K. Hyland,et al.  Aromatic amino acid decarboxylase deficiency in twins , 1990, Journal of Inherited Metabolic Disease.

[9]  P. Greengard,et al.  The renal dopamine system. , 1998, Advances in pharmacology.

[10]  F. Hanefeld,et al.  Aromatic L-amino acid decarboxylase deficiency: an extrapyramidal movement disorder with oculogyric crises. , 1997, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

[11]  W. Lovenberg,et al.  Aromatic L-amino acid decarboxylase. , 1962, The Journal of biological chemistry.