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9. Deoxyguanosine kinase deficiency: natural history and liver transplant outcome

10. Application of a Deep Learning System to Detect Papilledema on Nonmydriatic Ocular Fundus Photographs in an Emergency Department

11. Contributors

13. Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant

14. Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial

16. Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophy

18. New insights into idebenone therapy in relation to NQO1

19. Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

20. AFG3L2 and ACO2-linked Dominant Optic Atrophy: genotype-phenotype characterization compared to OPA1 patients

21. Optic nerve head dimension as biomarker in Leber hereditary optic neuropathy

26. Clinical study of FDXR-related mitochondriopathy: genotype-phenotype correlation and proposal of ancestry-based carrier screening in the Mexican population

28. IL NODO DI TEANO

29. PERCORSI E NODI

41. A multidisciplinary approach to estimating wolf population size for long‐term conservation

46. Childhood-Onset Leber Hereditary Optic Neuropathy—Clinical and Prognostic Insights

48. Deep Intronic LINE-1 Insertions in NF1: Expanding the Spectrum of Neurofibromatosis Type 1-Associated Rearrangements

49. Multimodal investigation of melanopsin retinal ganglion cells in Alzheimer's disease

50. The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10

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