Astrocytes are a specific immunological target in Rasmussen's encephalitis
Objective The current histopathological criteria of Rasmussen's encephalitis (RE) include
the presence of T‐cell–dominated inflammation, microglial activation, neuronal loss, and …
the presence of T‐cell–dominated inflammation, microglial activation, neuronal loss, and …
Left-right olfactory asymmetry results from antagonistic functions of voltage-activated calcium channels and the Raw repeat protein OLRN-1 in C. elegans
SL Bauer Huang, Y Saheki, MK VanHoven… - Neural …, 2007 - Springer
Background The left and right AWC olfactory neurons in Caenorhabditis elegans differ in
their functions and in their expression of chemosensory receptor genes; in each animal, one …
their functions and in their expression of chemosensory receptor genes; in each animal, one …
Slowly progressive hemiparesis in childhood as a consequence of Rasmussen encephalitis without or with delayed‐onset seizures
Five young children developed slowly progressive hemiparesis as the initial manifestation of
Rasmussen encephalitis (RE). Three have remained seizure free over an observational …
Rasmussen encephalitis (RE). Three have remained seizure free over an observational …
Focal chronic inflammatory epileptic encephalopathy in a patient with malformations of cortical development, with a review of the spectrum of chronic inflammatory …
RH Rhodes, RM Lehman, BY Wu, S Roychowdhury - Epilepsia, 2007 - Wiley Online Library
Purpose: Chronic cellular inflammation closely associated with epilepsy without an active
infection is a hallmark of Rasmussen encephalitis (RE). RE has typical and defining features …
infection is a hallmark of Rasmussen encephalitis (RE). RE has typical and defining features …
Gliomatosis cerebri mimicking Rasmussen encephalitis: case report
S Ghostine, R Raghavan, D Michelson… - Journal of …, 2007 - thejns.org
✓ Gliomatosis cerebri (GC) is a distinct malignant neuroepithelial neoplasm that is rarely
found in children. The authors present the case of an 11-year-old girl in whom the initial …
found in children. The authors present the case of an 11-year-old girl in whom the initial …
The history of Kazan neurological school
NK Amirov, EI Bogdanov, ME Guryleva… - Journal of the History …, 2007 - Taylor & Francis
The historical prerequisites for the foundation and teaching of neurology at Kazan University
are described; the relationship between the history of Kazan Imperial University Kazan …
are described; the relationship between the history of Kazan Imperial University Kazan …
Rasmussen encephalitis with ipsilateral brain stem involvement in an adult patient
CM Quesada, H Urbach, CE Elger… - Journal of Neurology …, 2007 - jnnp.bmj.com
Rasmussen encephalitis is a rare unihemispheric inflammatory disease of the brain that
leads to intractable seizures, cognitive decline and progressive neurological deficits …
leads to intractable seizures, cognitive decline and progressive neurological deficits …
Involvement of membrane channels in autoimmune disorders
Ion channels are ubiquitous transmembrane proteins that are involved in a wide variety of
cellular functions by selectively controlling the passage of ions across the plasma …
cellular functions by selectively controlling the passage of ions across the plasma …
Le syndrome de Rasmussen à début tardif: caractéristiques cliniques et thérapeutiques
V Jaillon-Riviere, S Dupont, F Bertran… - Revue …, 2007 - Elsevier
Résumé Le syndrome de Rasmussen (SR) est une maladie inflammatoire chronique
d'étiologie inconnue, caractérisée par une épilepsie sévère pharmacorésistante, un déficit …
d'étiologie inconnue, caractérisée par une épilepsie sévère pharmacorésistante, un déficit …
Acute intermittent porphyria, Rasmussen encephalitis, or both?
B Tziperman, BZ Garty, N Schoenfeld… - Journal of child …, 2007 - journals.sagepub.com
A case of a young woman who suffers from refractory epilepsy in the form of Rasmussen
encephalitis and acute intermittent porphyria is presented. The patient developed refractory …
encephalitis and acute intermittent porphyria is presented. The patient developed refractory …