Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Volumn 15, Issue 3-4, 2014, Pages 312-314

  Sakamoto, Hikaru ^a   Akamatsu, Maiko ^b   Hirano, Makito ^a   Saigoh, Kazumasa ^a   Ueno, Shuichi ^a   Isono, Chiharu ^a   Kusunoki, Susumu ^a   Nakamura, Yusaku ^a  

^a KINKI UNIVERSITY   (Japan)

^b Department of Neurology   (Japan)

Author keywords

Cerebellar and brainstem atrophy; Sensory neuropathy; Urinary incontinence; Urinary retention

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE; 4-HYDROXYBENZOATE POLYPRENYLTRANSFERASE; ALANINE; SUPEROXIDE DISMUTASE; TRANSFERASE; VALINE;

AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; BRAIN STEM; BRAIN STEM ATROPHY; BREATHING MUSCLE; CASE REPORT; CEREBELLUM ATROPHY; COPPER ZINC SUPEROXIDE DISMUTASE GENE; COQ2 GENE; FEMALE; GAIT DISORDER; GENE; GENE MUTATION; HETEROZYGOSITY; HUMAN; JAPANESE (PEOPLE); LACUNAR STROKE; LIMB WEAKNESS; MALE; MUSCLE ATROPHY; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCUTANEOUS ENDOSCOPIC GASTROSTOMY; PRIORITY JOURNAL; SHY DRAGER SYNDROME; SPINOCEREBELLAR DEGENERATION; URINARY DYSFUNCTION; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; BRAIN; GENETICS; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY;

ADULT; AGED; ALANINE; ALKYL AND ARYL TRANSFERASES; AMYOTROPHIC LATERAL SCLEROSIS; ASIAN CONTINENTAL ANCESTRY GROUP; BRAIN; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUTATION; SUPEROXIDE DISMUTASE; VALINE;

EID: 84901478861     PISSN: 21678421     EISSN: 21679223     Source Type: Journal    
DOI: 10.3109/21678421.2013.873051     Document Type: Article

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