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1 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 CatarinoLHON 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
2 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 CatarinoLHON 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
3 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 CatarinoLHON 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
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