Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations

Journal of Neurology

Volumn 261, Issue 9, 2014, Pages 1789-1793

  Liguori, Rocco ^a,b   Giannoccaro, Maria Pia ^b   Arnoldi, Alessia ^c   Citterio, Andrea ^c   Tonon, Caterina ^b,c   Lodi, Raffaele ^b,c   Bresolin, Nereo ^d,e   Bassi, Maria Teresa ^d  

^a IRCCS ISTITUTO DELLE SCIENZE NEUROLOGICHE DI BOLOGNA   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c UNIVERSITY OF BOLOGNA   (Italy)

^d SCIENTIFIC INSTITUTE   (Italy)

^e UNIVERSITY OF MILAN   (Italy)

Author keywords

Hereditary spastic paraplegia; Phosphorus magnetic resonance spectroscopy; Proton magnetic resonance spectroscopy; SPG28

Indexed keywords

PHOSPHOLIPASE;

ADOLESCENT; BRAIN; ENERGY METABOLISM; GENETIC PREDISPOSITION; GENETICS; HETEROZYGOTE; HUMAN; MALE; METABOLISM; MUSCLE; MUTATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PARAPLEGIA; PATHOLOGY; PEDIGREE; YOUNG ADULT;

ADOLESCENT; BRAIN; ENERGY METABOLISM; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MALE; MUSCLES; MUTATION; PARAPLEGIA; PEDIGREE; PHOSPHOLIPASES; YOUNG ADULT;

EID: 84939894258     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-014-7418-4     Document Type: Article

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