[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene

G. Cossu, C. Cella, M. Melis, A. Antonini, G. L. Floris, L. Ruffini, A. Spissu

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)167-168
Number of pages2
JournalNeurology
Volume64
Issue number1
Publication statusPublished - Jan 11 2005

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Cossu, G., Cella, C., Melis, M., Antonini, A., Floris, G. L., Ruffini, L., & Spissu, A. (2005). [123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene. Neurology, 64(1), 167-168.

[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene. / Cossu, G.; Cella, C.; Melis, M.; Antonini, A.; Floris, G. L.; Ruffini, L.; Spissu, A.

In: Neurology, Vol. 64, No. 1, 11.01.2005, p. 167-168.

Research output: Contribution to journalArticle

Cossu, G, Cella, C, Melis, M, Antonini, A, Floris, GL, Ruffini, L & Spissu, A 2005, '[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene', Neurology, vol. 64, no. 1, pp. 167-168.
Cossu G, Cella C, Melis M, Antonini A, Floris GL, Ruffini L et al. [123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene. Neurology. 2005 Jan 11;64(1):167-168.
Cossu, G. ; Cella, C. ; Melis, M. ; Antonini, A. ; Floris, G. L. ; Ruffini, L. ; Spissu, A. / [123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene. In: Neurology. 2005 ; Vol. 64, No. 1. pp. 167-168.
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