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TitleDateTypeSetname
201 Expanded Access Program (EAP) in Leber's Hereditary Optic Neuropathy (LHON) Patients Treated for 24 Months (PDF)2020-03Textehsl_novel_nam
202 Foveal Ganglion Cell Loss During Conversion of Leber Hereditary of Neuropathy2022-02Textehsl_novel_nam
203 The Impact of LHON on the Quality of Life of Patients and Their Relatives2022-02Textehsl_novel_nam
204 Late recovery of function after oculomotor nerve palsy.ehsl_novel_jno
205 Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation.ehsl_novel_jno
206 Long Term Treatment with Idebenone in Leber's Hereditary Optic Neuropathy (LHON): Real World Clinical Practice2018-03Textehsl_novel_nam
207 Mitochondrial Dysfunction in Patients With Nonarteritic Anterior Ischemic Optic Neuropathy and Optic Disc Drusen2022-02Textehsl_novel_nam
208 Negative ERG in Hereditary Optic Neuropathies2017Textehsl_novel_nam
209 Retrograde Transport to Retinal Ganglion Cells: An Alternative Strategy for Gene Delivery in Optic Neuropathies2022-02Textehsl_novel_nam
210 Severe Bilateral Optic Neuropathy Secondary to Cobalt Toxicity in Genetically-Predisposed Individual2022-02Textehsl_novel_nam
211 A Multiple Sclerosis-Like Illness in a Man Harboring the LHOM 14484 Mutation1998-03-23Textehsl_novel_nam
212 Leber Hereditary Optic Neuropathy (LHON): a novel mutation?2012-02-14Textehsl_novel_nam
213 Leber Hereditary Optic Neuropathy G11778A Gene Therapy Clinical Trial: Serial Pretreatment Evaluation from Baseline to Two Years2012-02-13Textehsl_novel_nam
214 Macular Microcystic Changes on OCT in Optic Neuropathy2014-03-04Textehsl_novel_nam
215 Melanopsin Retinal Ganglion Cells: A New Class of Cells in Human Retina2009-02-23Textehsl_novel_nam
216 Mitochondrial Optic Neuropathies (MON)Textehsl_novel_aas
217 Page 31Textehsl_novel_nam
218 Visual Recovery in a Case of LHON with 3460 mtDNA Mutation1996-02-12Textehsl_novel_nam
219 Walsh & Hoyt: Leber's Optic Neuropathy2005Textehsl_novel_whts
220 "Sporadic"Leber's Hereditary Optic Neuropathy1991-02-26Textehsl_novel_nam
221 Bilateral optic atrophy with novel MTTL 3268 A>G homoplasmy - LHON variant or not?2012-02-14Textehsl_novel_nam
222 LHON-MS patient with long-term non-response to Idebenone shows improvement after 4-AP Usage2019-03Textehsl_novel_nam
223 Presentation of Vision Loss and Subsequent Recovery in a Patient with Features of LHON-MS (Harding's Disease)2023-03-14Textehsl_novel_nam
224 Irreversible optic neuropathy in wernicke encephalopathy and leber hereditary optic neuropathy.ehsl_novel_jno
225 Subject Indexehsl_novel_jno
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