Leber's hereditary optic neuropathy with intracranial arteriovenous malformation: A case report

Acta Neurologica Belgica

Volumn 102, Issue 2, 2002, Pages 82-86

  Fujitake, Junko ^a   Mizuta, Haruo ^a   Fujii, Hayato ^a   Ishikawa, Yasuhiro ^a   Sasamoto, Kenji ^a   Goto, Yu Ichi ^a   Nonaka, Ikuya ^a   Tatsuoka, Yoshihisa ^a  

^a KYOTO CITY HOSPITAL   (Japan)

Author keywords

Arteriovenous malformation (AVM); Leber's hereditary optic neuropathy (LHON); Mitochondrial DNA

Indexed keywords

METHYLPREDNISOLONE; MITOCHONDRIAL DNA; NUCLEOTIDE; UBIDECARENONE;

ARTICLE; BRAIN ARTERIOVENOUS MALFORMATION; BRAIN VENTRICLE; CASE REPORT; CORTICOSTEROID THERAPY; GENE MUTATION; GENETIC ANALYSIS; HEREDITARY OPTIC ATROPHY; HUMAN; MALE; POINT MUTATION; SCHOOL CHILD; SURGICAL DRAINAGE; ADOLESCENT; GENETICS; LEBER HEREDITARY OPTIC NEUROPATHY; MUTATION; PATHOPHYSIOLOGY; RADIOGRAPHY;

ADOLESCENT; DNA, MITOCHONDRIAL; HUMANS; INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; MALE; MUTATION; OPTIC ATROPHY, HEREDITARY, LEBER;

EID: 0035992367     PISSN: 03009009     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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