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Fahr syndrome: Difference between revisions
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[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247864/pdf/PAMJ-18-287.pdf Syndrome de Fahr : une complication rare de la radiothérapie cérébrale survenant chez un patient acromégale] | [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247864/pdf/PAMJ-18-287.pdf Syndrome de Fahr : une complication rare de la radiothérapie cérébrale survenant chez un patient acromégale] | ||
[https://www.jstage.jst.go.jp/article/yakushi/134/12/134_14-00209-3/_pdf 原因遺伝子からみたパーキンソニズムを呈する疾患とその治療戦略] | |||
<references/> | <references/> | ||
[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 18:29, 24 August 2015
The Fahr syndrome, is a rare neurological disease characterized by calcified deposits[1]
Disease classification WHO
Fahr G23.8
Links
Quantitative MR Markers and Psychiatric Symptoms in a Patient with Fahr Disease
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Saleem et al. Orphanet Journal of Rare Diseases 2013, 8:156
Syndrome de Fahr : une complication rare de la radiothérapie cérébrale survenant chez un patient acromégale 原因遺伝子からみたパーキンソニズムを呈する疾患とその治療戦略