An unusual gait following the discovery of a new disease

Practical Neurology

Volumn 11, Issue 2, 2011, Pages 81-84

  Keogh, M J ^a,b   Khan, A ^a   Gorman, G ^a   McNeill, A ^c   Horvath, R ^a,b   Burn, J ^b   Chinnery, P F ^a,b  

^a ROYAL VICTORIA INFIRMARY   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

^c ROYAL FREE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; DYSTONIA; EXTRAPYRAMIDAL SYNDROME; FEMALE; GENETICS; HUMAN; IRON METABOLISM DISORDER; NEUROAXONAL DYSTROPHY; NEUROFERRITINOPATHY; NEUROLOGIC DISEASE; PATHOLOGY;

ADULT; BASAL GANGLIA DISEASES; DYSTONIA; FEMALE; GAIT DISORDERS, NEUROLOGIC; HUMANS; IRON METABOLISM DISORDERS; NEUROAXONAL DYSTROPHIES;

EID: 79952804714     PISSN: 14747758     EISSN: 14747766     Source Type: Journal    
DOI: 10.1136/jnnp.2011.242230     Document Type: Article

References (2)

1. Chinnery PF, Crompton DE, Birchall D, et al. Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation. Brain 2007;130:110-19.
2. and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation. Neurology 2008;70:1614-19.