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Publications by Maria Lucia Valentino
Hearing Dysfunction in a Large Family Affected by Dominant Optic Atrophy (OPA8-Related DOA): A Human Model of Hidden Auditory Neuropathy
Frontiers in Neuroscience
Neuroscience
Haplogroup Effects and Recombination of Mitochondrial DNA: Novel Clues From the Analysis of Leber Hereditary Optic Neuropathy Pedigrees
American Journal of Human Genetics
Genetics
Related publications
A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
A Family With Apparently Sex-Linked Optic Atrophy.
Journal of Medical Genetics
Genetics
Progressive Auditory Neuropathy in Patients With Leber's Hereditary Optic Neuropathy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
A Novel Missense OPA1 Mutation in a Patient With Dominant Optic Atrophy and Cervical Dystonia
Movement Disorders Clinical Practice
Neurology
Electrophysiological and Histologic Assessment of Retinal Ganglion Cell Fate in a Mouse Model forOPA1-Associated Autosomal Dominant Optic Atrophy
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Primate Model of Nonarteritic Anterior Ischemic Optic Neuropathy
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Hereditary Optic Atrophy With Dominant Transmission and Early Onset
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Homozygosity Mapping of Spinocerebellar Ataxia With Cerebellar Atrophy and Peripheral Neuropathy to 9q33–34, and With Hearing Impairment and Optic Atrophy to 6p21–23
European Journal of Human Genetics
Genetics
Changes in the Sella Turcica in Family Optic Atrophy
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
