New neuropathological findings in Unverricht–Lundborg disease: neuronal intranuclear and cytoplasmic inclusions

NEUROPATHOLOGICAL STUDIES IN THREE SCANDINAVIAN CASES OF PROGRESSIVE MYOCLONUS EPILEPSY

(2010) MATTI HALTIA et al.   ACTA NEUROLOGICA SCANDINAVICA

PROGRESSIVE MYOCLONUS EPILEPSY

(2010) M. Koskiniemi et al.   ACTA NEUROLOGICA SCANDINAVICA

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

(2010) Hazel Urwin et al.   ACTA NEUROPATHOLOGICA

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

(2009) Manuela Neumann et al.   ACTA NEUROPATHOLOGICA

FUS pathology in basophilic inclusion body disease

(2009) David G. Munoz et al.   ACTA NEUROPATHOLOGICA

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

(2009) Ian R. A. Mackenzie et al.   ACTA NEUROPATHOLOGICA

Rethinking ALS: The FUS about TDP-43

(2009) Clotilde Lagier-Tourenne et al.   CELL

Altered cortical inhibition in Unverricht–Lundborg type progressive myoclonus epilepsy (EPM1)

(2009) Nils Danner et al.   EPILEPSY RESEARCH

A Role for Ubiquitin in Selective Autophagy

(2009) Vladimir Kirkin et al.   MOLECULAR CELL

Motor cortex and thalamic atrophy in Unverricht-Lundborg disease: Voxel-based morphometric study

(2009) P. Koskenkorva et al.   NEUROLOGY

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6

(2009) C. Vance et al.   SCIENCE

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

(2009) T. J. Kwiatkowski et al.   SCIENCE

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

(2008) Ian R. A. Mackenzie et al.   BRAIN

The natural history of Unverricht-Lundborg disease: A report of eight genetically proven cases

(2007) Nee K. Chew et al.   MOVEMENT DISORDERS