Episodic Neurological Dysfunction (Epilepsy), Clinicians and Flying
نویسندگان
چکیده
منابع مشابه
P8: Temporal Lobe Epilepsy and Mitochondrial Dysfunction
لطفاً به چکیده انگلیسی مراجعه شود.
متن کاملEpisodic Neurological Channelopathies
Inherited episodic neurological disorders are often due to mutations in ion channels or their interacting proteins, termed channelopathies. There are a wide variety of such disorders, from those causing paralysis, to extreme pain, to ataxia. A common theme in these is alteration of action potential properties or synaptic transmission and a resulting increased propensity of the resulting tissue ...
متن کاملP12: Mitochondrial Dysfunction and Oxidative Stress in Epilepsy
لطفاً به چکیده انگلیسی مراجعه شود.
متن کاملDysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
The molecular basis of idiopathic generalized epilepsy remains poorly understood. Absence epilepsy with 3 Hz spike-wave EEG is one of the most common human epilepsies, and is associated with significant morbidity. Several spontaneously occurring genetic mouse models of absence epilepsy are caused by dysfunction of the P/Q-type voltage-gated calcium channel CaV2.1. Such mice exhibit a primary ge...
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ژورنال
عنوان ژورنال: Medical Journal of Shree Birendra Hospital
سال: 1999
ISSN: 2091-0193,2091-0185
DOI: 10.3126/mjsbh.v2i0.21479