Latest papers

Motor and visuospatial abilities in a model of olivocerebellar and retinal degeneration--Lurcher mutant mice of C3H strain.

[Pontocerebellar hypoplasia type 1: a case report].

Olivopontocerebellar atrophy: toward a better nosological definition.

Severe, fetal-onset form of olivopontocerebellar hypoplasia in three sibs: PCH type 5?

Cerebellar ataxia and snoring.

Changes in proliferation activity and relative distributions of lymphoid cell subpopulations in congenitally athymic nu/nu mice and Lurcher mice with spontaneous olivopontocerebellar degeneration.

Comparison of embryonic cerebellar graft survival in adult Lurcher mutant mice of strains C3H and C57Bl/7.

Does transplantation of cerebellar embryonic tissue influence hippocampal LTP in adult Lurcher mutant mice?

Neural functional and morphological consequences of retinal degeneration in C3H Lurcher mutant and wild type mice.

Autonomic nervous evaluation in the early stages of olivopontocerebellar atrophy.

X-linked adrenoleukodystrophy with olivopontocerebellar atrophy.

Grading of neuropathology in multiple system atrophy: Proposal for a novel scale

FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.

[Analysis of brain images in patients with spinocerebellar degeneration; using statistical parametric mapping (SPM) and easy Z score imaging system (eZIS)].

[Improvements in the symptoms of olivopontocerebellar atrophy with gabapentin]

Cognitive affective psychosis syndrome in a patient with sporadic olivopontocerebellar atrophy.

Functional consequences of retinal degeneration in spatial orientation in C3H wild type and Lurcher mutant mice.

Effect of whole-body exposure to high-frequency electromagnetic field on the brain electrogeny in neurodefective and healthy mice.

[Spinal muscular atrophy associated with olivopontocerebellar hypoplasia. A case report].

Various methods of Purkinje cells transplantation and their functional response in Lurcher mutant mice.