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Title | Creator | Description | Identifier |
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Expanded Access Program (EAP) in Leber's Hereditary Optic Neuropathy (LHON) Patients Treated for 24 Months (Slides) | Thomas Klopstock, Xavier Llòria, Magda Silva, Rudolph Guenther, Felice Lob, Bettina Von Livonius, Claudia Catarino | LHON is a mitochondrial genetic disorder resulting in severe bilateral central VA loss. Three primary mitochondrial DNA mutations cause over 90% of cases. Data from idebenone EAP for patients with LHON receiving treatment for at least 24 months were analyzed to assess rate of clinically-relevant rec... | 20200310_nanos_sciplatform3_06-slides |
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Expanded Access Program (EAP) in Leber's Hereditary Optic Neuropathy (LHON) Patients Treated for 24 Months (PDF) | Thomas Klopstock, Xavier Llòria, Magda Silva, Rudolph Guenther, Felice Lob, Bettina Von Livonius, Claudia Catarino | LHON is a mitochondrial genetic disorder resulting in severe bilateral central VA loss. Three primary mitochondrial DNA mutations cause over 90% of cases. Data from idebenone EAP for patients with LHON receiving treatment for at least 24 months were analyzed to assess rate of clinically-relevant rec... | 20200310_nanos_sciplatform3_06-pdf |
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Expanded Access Program (EAP) in Leber's Hereditary Optic Neuropathy (LHON) Patients Treated for 24 Months (Video) | Thomas Klopstock, Xavier Llòria, Magda Silva, Rudolph Guenther, Felice Lob, Bettina Von Livonius, Claudia Catarino | LHON is a mitochondrial genetic disorder resulting in severe bilateral central VA loss. Three primary mitochondrial DNA mutations cause over 90% of cases. Data from idebenone EAP for patients with LHON receiving treatment for at least 24 months were analyzed to assess rate of clinically-relevant rec... | 20200310_nanos_sciplatform3_06 |