Central Tegmental Tract Involvement in an Infant with 6-Pyruvoyltetrahydropterin Synthetase Deficiency

References

1. ↵
   Blau N, Thony B, Cotton RGH, et al. Disorders of tetrahydrobiopterin and related biogenic amines. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic and molecular bases of inherited disease. 8th ed. New York: McGraw-Hill;2001 :1725–76
2. ↵
   Chien YH, Chiang SC, Huang A, et al. Treatment and outcome of Taiwanese patients with 6-pyruvoyltetrahydropterin synthetase gene mutation. J Inherit Metab Dis 2001;24:815–23

   CrossRefPubMedWeb of Science
3. ↵
   Chien YH, Peng SF, Wang TR, et al. Cranial MR spectroscopy of tetrahydrobiopterin deficiency. AJNR Am J Neuroradiol 2002;23:1055–58

   Abstract/FREE Full Text
4. ↵
   Brody BA, Kinney HC, Kloman AS, et al. Sequence of central nervous system myelination in human infancy. I. An autopsy study of myelination. J Neuropathol Exp Neurol 1987;46:283–301

   PubMedWeb of Science
5. ↵
   Van der Knaap MS, Barth PG, Gabreëls FJM, et al. A new leukoencephalopathy with vanishing white matter. Neurology 1997;48:845–55

   Abstract/FREE Full Text
6. Khong PL, Lam BCC, Chung BHY, et al. Diffusion-weighted MR imaging in neonatal nonketotic hyperglycinemia. AJNR Am J Neuroradiol 2003;24:1181–83

   Abstract/FREE Full Text
7. ↵
   Tada H, Takanashi J, Barkovich AJ, et al. Reversible white matter lesion in methionine adenosyltransferase I/III deficiency. AJNR Am J Neuroradiol 2004;25:1843–45

   Abstract/FREE Full Text
8. ↵
   Rossi A, Biancheri R, Bruno C, et al. Leigh syndrome with COX deficiency and. SURF1 gene mutations: MR imaging findings. AJNR Am J Neuroradiol 2003;24:1188–91

   Abstract/FREE Full Text