(Q48107633)

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Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

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Patrick Chariot

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

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Brugières P

2

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Europe PubMed Central

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8 February 2018

http://europepmc.org/abstract/MED/10495052

Eliezer-Vanerot MC

3

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

Gény C

4

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

Binaghi M

5

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Europe PubMed Central

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8 February 2018

http://europepmc.org/abstract/MED/10495052

Césaro P

6

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8 February 2018

http://europepmc.org/abstract/MED/10495052

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1 September 1999

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8 February 2018

http://europepmc.org/abstract/MED/10495052

Movement Disorders

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PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

14

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

5

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

855-859

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisal

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Reversible chorea in primary antiphospholipid syndrome

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21 January 2018

Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS study

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Sporadic Leber hereditary optic neuropathy in Australia and New Zealand

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21 January 2018

Leber's hereditary optic neuropathy plus dystonia is caused by a mitochondrial DNA point mutation

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21 January 2018

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

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21 January 2018

Remarkable recovery of visual function in a patient with Leber's optic neuropathy and multiple mutations of mitochondrial DNA

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The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

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Identifiers

10.1002/1531-8257(199909)14:5<855::AID-MDS1023>3.0.CO;2-9

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10495052

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