Filters: Subject: "Mitochondrial DNA"
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TitleDateTypeSetname
1 A Tale of Progressive Painless Vision Loss in a 64-Year-Old Man Due to Leber Hereditary Optic Neuropathy2022-09Textehsl_novel_jno
2 Cross-Sectional Analysis of Baseline Visual Parameters in Subjects Recruited Into the RESCUE and REVERSE ND4-LHON Gene Therapy Studies2021-09Textehsl_novel_jno
3 Cuban Epidemic Optic Neuropathy1996-09Textehsl_novel_jno
4 Evolution, living patterns, and mitochondrial genetic variations in chimpanzees2015-12Textir_htoa
5 Genetic admixture in the Late Pleistocene1994-12Textir_htca
6 Genetic evidence on modern human origins1995Textir_uspace
7 The Genetic Testing Paradigm for Leber's Hereditary Optic Neuropathy: Discovery of a New Candidate LHON Mitochondrial DNA Mutation2004-03-31Textehsl_novel_nam
8 The Impact of Leber Hereditary Optic Neuropathy on the Quality of Life of Patients and Their Relatives: A Qualitative Study2022-09Textehsl_novel_jno
9 Leber Hereditary Optic Neuropathy Caused by a Mitochondrial DNA 10663T>C Point Mutation and Its Response to Idebenone Treatment2018-03Textehsl_novel_jno
10 Leber's Optic Neuropathy Treated with Idebenone1995-02-21Textehsl_novel_nam
11 Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study2021-09Textehsl_novel_jno
12 Magnetic Resonance Imaging Findings in the Pregeniculate Visual Pathway in Leber Hereditary Optic Neuropathy2022-03Textehsl_novel_jno
13 Mitochondrial DNA Mutations in Cuban Optic and Peripheral Neuropathy1996-09Textehsl_novel_jno
14 Optic Nerve and Retinal Changes in Leber's Hereditary Optic Neuropathy (LHON) with 11778 and 3460 mt DNA Mutations: A Comparative Light and Electronmicroscopic Study1999-03-15Textehsl_novel_nam
15 Pattern of Retinal Ganglion Cell Loss in Dominant Optic Atrophy due to OPA1 Mutations2011-02-08Textehsl_novel_nam
16 Spatial and temporal stability of mtDNA haplogroup frequencies in native North America2000Textir_uspace
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