منابع مشابه
HLA and complement typing in olivo-ponto-cerebellar atrophy.
HLA antigen typing was carried out in a family with an autosomal dominant form of spinocerebellar degeneration [possibly olivoponto cerebellar atrophy (O.P.C.A.)--Type 1]. Eleven ataxic patients, three possibly ataxic subjects, two unrelated spouses and 13 clinically normal at risk siblings were typed for ABO and Rh blood groups, HLA-A and HLA-B antigens, C4 component of the complement and a nu...
متن کاملDevelopment of Axon-Target Specificity of Ponto-Cerebellar Afferents
The function of neuronal networks relies on selective assembly of synaptic connections during development. We examined how synaptic specificity emerges in the pontocerebellar projection. Analysis of axon-target interactions with correlated light-electron microscopy revealed that developing pontine mossy fibers elaborate extensive cell-cell contacts and synaptic connections with Purkinje cells, ...
متن کاملTumour of the glomus jugulare (non-chromaffin paraganglioma) of the ponto-cerebellar angle treated with x-irradiation.
Tumours of the glomus jugulare expanding into the posterior fossa are of the utmost rarity. Most such tumours originate primarily in the middle ear and later tend to expand in the direction of the external auditory canal. They are, therefore, recognized as a rule at an otoscopic examination and, consequently, most references to this tumour are found in the oto-laryngological literature. Accordi...
متن کاملCholesteatoma of cerebellopontine angle presented as trigeminal neuralgia.
Cholesteatoma in the cerebellopontine angle presented as trigeminal neuralgia are not common. Between 2010 and 2013, 12 such patients were operated on in our department. Those patients included 8 females and 4 males with an average age of 47.8 years. One patient was combined with the ipsilateral hemifacial spasm. Five patients had hypesthesia in the ipsilateral side of the face. During the surg...
متن کاملTeaching NeuroImages: Diffusion tensor tractography of cortico-ponto-cerebellar pathways in Rasmussen encephalitis.
A 34-year-old man developed since age 18 years epilepsia partialis continua followed over the years by progressive ataxic hemiparesis involving the left side (figure 1). Structural cerebral abnormalities, mitochondrial diseases, and known autoimmune disorders were excluded. Cerebral MRI showed progressive right cerebral and crossed left cerebellar hemiatrophy (figure 2, A and B). Tractography o...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1921
ISSN: 0035-9157
DOI: 10.1177/003591572101400924