论文信息 - Leukoencephalopathy with vanishing white matter: report of four cases from three unrelated Brazilian families - 字舞流文

Leukoencephalopathy with vanishing white matter: report of four cases from three unrelated Brazilian families

S. Rosemberg | C. Leite | M. C. Lacerda | F. Arita | S. Kliemann

[1] K. Takeshita,et al. A Japanese girl with leukoencephalopathy with vanishing white matter , 2001, Brain and Development.

[2] I. Saatci,et al. A case of leukoencephalopathy with vanishing white matter. , 2000, Neuropediatrics.

[3] F. Gabreëls,et al. Increased Cerebrospinal Fluid Glycine: A Biochemical Marker for a Leukoencephalopathy With Vanishing White Matter , 1999, Journal of child neurology.

[4] S. Naidu,et al. The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27. , 1999, American journal of human genetics.

[5] J. Valk,et al. Phenotypic variation in leukoencephalopathy with vanishing white matter , 1998, Neurology.

[6] F. Gabreëls,et al. A new leukoencephalopathy with vanishing white matter , 1997, Neurology.

[7] R. Schiffmann,et al. Childhood ataxia with diffuse central nervous system hypomyelination , 1994, Annals of neurology.

[8] J. Frahm,et al. Diffuse White Matter Disease in Three Children: An Encephalopathy with Unique Features on Magnetic Resonance Imaging and Proton Magnetic Resonance Spectroscopy , 1993, Neuropediatrics.