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Acta Neuropathologica
|
August 15, 2012
The genetics and neuropathology of frontotemporal lobar degeneration
Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology
|
June 26, 2007
No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease
Sebastiaan Engelborghs, Kristel Sleegers, Patrick Cras, et al.
Neuromuscular Disorders : NMD
|
January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entity
Jonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.
Brain Pathology (Zurich, Switzerland)
|
December 6, 2003
Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency
Peter C G Nijssen, Chantal Ceuterick, Otto P van Diggelen, et al.
Archives of Neurology
|
December 19, 2006
Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes
Yunhong Bai, Emilia Ianokova, Qin Pu, et al.
The American Journal of Pathology
|
April 17, 2010
DNAJB2 expression in normal and diseased human and mouse skeletal muscle
Kristl G Claeys, Magdalena Sozanska, Jean-Jacques Martin, et al.
Journal of Neuropathology and Experimental Neurology
|
May 3, 2006
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
Daniel Pirici, Rik Vandenberghe, Rosa Rademakers, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 21, 2012
Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy
Emmanuel Scalais, Baudouin Francois, Patrick Schlesser, et al.
Annals of Neurology
|
July 12, 2002
Periaxin mutations cause a broad spectrum of demyelinating neuropathies
Hiroshi Takashima, Cornelius F Boerkoel, Peter De Jonghe, et al.
Brain : a Journal of Neurology
|
August 26, 2006
Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease
Nathalie Brouwers, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 107) with videos related to
Sort By:
Page
of 11
Acta Neuropathologica
|
August 15, 2012
The genetics and neuropathology of frontotemporal lobar degeneration
Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, et al.
Brain : a Journal of Neurology
|
June 26, 2007
No association of CSF biomarkers with APOEepsilon4, plaque and tangle burden in definite Alzheimer's disease
Sebastiaan Engelborghs, Kristel Sleegers, Patrick Cras, et al.
Neuromuscular Disorders : NMD
|
January 27, 2009
Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entity
Jonathan Baets, Ines Dierick, Chantal Ceuterick-de Groote, et al.
Brain Pathology (Zurich, Switzerland)
|
December 6, 2003
Autosomal dominant adult neuronal ceroid lipofuscinosis: a novel form of NCL with granular osmiophilic deposits without palmitoyl protein thioesterase 1 deficiency
Peter C G Nijssen, Chantal Ceuterick, Otto P van Diggelen, et al.
Archives of Neurology
|
December 19, 2006
Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes
Yunhong Bai, Emilia Ianokova, Qin Pu, et al.
The American Journal of Pathology
|
April 17, 2010
DNAJB2 expression in normal and diseased human and mouse skeletal muscle
Kristl G Claeys, Magdalena Sozanska, Jean-Jacques Martin, et al.
Journal of Neuropathology and Experimental Neurology
|
May 3, 2006
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
Daniel Pirici, Rik Vandenberghe, Rosa Rademakers, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 21, 2012
Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathy
Emmanuel Scalais, Baudouin Francois, Patrick Schlesser, et al.
Annals of Neurology
|
July 12, 2002
Periaxin mutations cause a broad spectrum of demyelinating neuropathies
Hiroshi Takashima, Cornelius F Boerkoel, Peter De Jonghe, et al.
Brain : a Journal of Neurology
|
August 26, 2006
Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease
Nathalie Brouwers, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Page
of 11