A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in <i>MT-ND4</i> Gene (<i>m.1125...

by Rasa Liutkeviciene, Agne Sidaraite, Lina Kuliaviene, Brigita Glebauskiene, Neringa Jurkute, Lina Aluzaite-Baranauskiene, Arvydas Gelzinis, Reda Zemaitiene
Published 2021-02-01

Intravitreal Gene Therapy vs. Natural History in Patients With Leber Hereditary Optic Neuropathy Carrying the m.11778G>A ND4 Mutation: Systematic Review and Indirect Comparison

by Nancy J. Newman, Patrick Yu-Wai-Man, Patrick Yu-Wai-Man, Patrick Yu-Wai-Man, Patrick Yu-Wai-Man, Valerio Carelli, Valerio Carelli, Valerie Biousse, Mark L. Moster, Catherine Vignal-Clermont, Catherine Vignal-Clermont, Robert C. Sergott, Thomas Klopstock, Thomas Klopstock, Thomas Klopstock, Alfredo A. Sadun, Jean-François Girmens, Chiara La Morgia, Adam A. DeBusk, Neringa Jurkute, Neringa Jurkute, Claudia Priglinger, Rustum Karanjia, Rustum Karanjia, Constant Josse, Julie Salzmann, François Montestruc, Michel Roux, Magali Taiel, José-Alain Sahel, José-Alain Sahel, José-Alain Sahel, José-Alain Sahel
Published 2021-05-01