Mapping of Purkinje Neuron Loss and Polyglucosan Body Accumulation in Hereditary Cerebellar Degeneration in Scottish Terriers

Glycogen hyperphosphorylation underlies lafora body formation

(2010) Julie Turnbull et al.   ANNALS OF NEUROLOGY

Laforin, the most common protein mutated in Lafora disease, regulates autophagy

(2010) Carmen Aguado et al.   HUMAN MOLECULAR GENETICS

Genetic Depletion of the Malin E3 Ubiquitin Ligase in Mice Leads to Lafora Bodies and the Accumulation of Insoluble Laforin

(2010) Anna A. DePaoli-Roach et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Hereditary Cerebellar Degeneration in Scottish Terriers

(2010) G. Urkasemsin et al.   JOURNAL OF VETERINARY INTERNAL MEDICINE

Development of the Human Cerebellum and Its Disorders

(2009) Hans J. ten Donkelaar et al.   CLINICS IN PERINATOLOGY

Novel role of transglutaminase 1 in corpora amylacea formation?

(2009) Micha M.M. Wilhelmus et al.   NEUROBIOLOGY OF AGING

Ubiquitin, the proteasome and protein degradation in neuronal function and dysfunction

(2008) Hwan-Ching Tai et al.   NATURE REVIEWS NEUROSCIENCE

Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: Clinicopathological study of four autopsy cases

(2008) Satoru Ota et al.   NEUROPATHOLOGY

Characterisation of Lafora-like bodies and other polyglucosan bodies in two aged dogs with neurological disease

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