Leber's hereditary optic neuropathy with dystonia in a Japanese family
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference14 articles.
1. Dystonia;Fahn,2000
2. The early-onset torsion dystonia gene (DYT-1) encodes an ATP-binding protein;Ozelius;Nat Genet,1997
3. Uber hereditare und congenital angelegte Sehnervenleiden;Leber;Arch Ophthalmol,1871
4. Leber's “plus”: neurological abnormalities in patients with Leber's hereditary optic neuropathy;Nikoskelainen;J Neurol Neurosurg Psychiatry,1995
5. Leber's hereditary optic neuropathy, new genetic consideration;Newman;Arch Neurol,1993
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1. Hemi dystonia from a mitochondrial mutation in MT-ND6;JAP Academy Journal;2023-06-04
2. Leber Mitochondrial Optic Neuropathy in Pediatric Females With Focus on Very Early Onset Cases;Journal of Child Neurology;2023-01-19
3. A Novel Variation in the Mitochondrial Complex I Assembly Factor NDUFAF5 Causes Isolated Bilateral Striatal Necrosis in Childhood;Frontiers in Neurology;2021-06-10
4. Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation;Neurological Sciences;2021-03-29
5. Clinical characteristics and diagnostic clues to Neurometabolic causes of dystonia;Journal of the Neurological Sciences;2020-12
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