Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult

T. Birnbaum; H.J. Blom; H. Prokisch; M. Hartig; T. Klopstock

doi:10.1007/s00415-008-0043-3

Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult

T. Birnbaum, H.J. Blom, H. Prokisch, M. Hartig, T. Klopstock

Clinical chemistry

Research output: Contribution to journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	1845-1846
Journal	Journal of Neurology
Volume	255
Issue number	11
DOIs	https://doi.org/10.1007/s00415-008-0043-3
Publication status	Published - 2008

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10.1007/s00415-008-0043-3

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Birnbaum, T., Blom, H. J., Prokisch, H., Hartig, M., & Klopstock, T. (2008). Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult. Journal of Neurology, 255(11), 1845-1846. https://doi.org/10.1007/s00415-008-0043-3

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Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult. / Birnbaum, T.; Blom, H.J.; Prokisch, H.; Hartig, M.; Klopstock, T.

In: Journal of Neurology, Vol. 255, No. 11, 2008, p. 1845-1846.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Prokisch, H.

AU - Hartig, M.

AU - Klopstock, T.

PY - 2008

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JO - Journal of Neurology

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