Behçet’s disease is a multisystem inflammatory disorder with unknown aetiology. It is a disease
of young adults with a more severe course in males subjects. Its prevalence is high in the …

Andersen's syndrome is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic
features. We have mapped an Andersen's locus to chromosome 17q23 maximum LOD…

In order to define the patterns of neurological involvement in Behçet's disease and to assess
prognostic factors, 558 files of the neuro-Behçet out-patient clinic were reviewed. Those …

• We investigated the prevalence and type of neurologic involvement in Behçet's syndrome
in a prospective protocol. Of 323 consecutive patients with Behçet's syndrome seen during a …

We analyzed the data obtained from neuropsychological evaluations of 12 neuro-Behçet
Disease (NBD) patients who had been followed up for 35.6 ± 23.7 months with successive …

Cytokines and chemokines in cerebrospinal fluid (CSF) can have implications on the
pathogenesis of neuro-Behçet's disease (NB). CSF and serum samples from 33 patients with NB, …

αB-Crystallin, a small heat shock protein, is an immuno-dominant antigen with increased
tissue expression in demyelination. To investigate the humoral response against αB-crystallin, …

Pompe disease is an autosomal recessive lysosomal glycogen storage disorder, characterized
by progressive muscle weakness. Deficiency of acid α‐glucosidase (EC; 3.2.1.20/3) can …

In 10 10 inclusion body myositis (IBM) patients and 2 2 oculopharyngeal muscular
dystrophy (OPMD) patients, vacuolated muscle fibers contained darkly stained ubiquitin (Ub)-…

Autosomal recessive demyelinating Charcot–Marie–Tooth disease (CMT4), Dejerine–Sottas
disease and congenital hypomyelinating neuropathy are variants of hereditary …