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Neurologic features of Hutchinson-Gilford progeria syndrome after lonafarnib treatment
OBJECTIVES: The objective of this study was to retrospectively evaluate neurologic status pre- and posttreatment with the oral farnesyltransferase inhibitor lonafarnib in children with Hutchinson-Gilford progeria syndrome (HGPS), a rare, fatal disorder of segmental premature aging that results in ea...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Lippincott Williams & Wilkins
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3776537/ https://ncbi.nlm.nih.gov/pubmed/23897869 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e31829d85c0 |
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