Epileptic Amnesic Syndrome: An Update and Further Considerations
نویسندگان
چکیده
منابع مشابه
Calcium and Vitamin D Metabolism in Pediatric Nephrotic Syndrome; An Update on the Existing Literature
Minimal Change Disease (MCD) is the leading cause of childhood Nephrotic Syndrome (NS). Therefore in pediatrics nephrotic syndrome, most children beyond the first year of life will be treated with corticosteroids without an initial biopsy. Children with NS often display a number of calcium homeostasis disturbances causing abnormal bone histology, including hypocalcemia, reduced serum vitamin D...
متن کاملFurther Analysis of the Hippocampal Amnesic Syndrome: 14-year Follow-up Study of H.m.*
-The report attempts to delineatecertain residual learning capacities of H.M., a young man who became amnesic in 1953 following a bilateral removal in the hippocampal zone. In addition to being able to acquire new motor skills (CoRKIN [2]), this patient shows some evidence of perceptual learning. He also achieves some retention of very simple visual and tactual mazes in which the sequence of re...
متن کاملFurther considerations on the so-called Rowell syndrome.
The recent article by Solanki, et al. [1] described a further case of Rowell Syndrome (RS), that is a long debated nosological entity, historically defined as a unique clinical association between cutaneous lupus erythematosus (CLE) with erythema multiforme (EM) like lesions and characteristic immunologic pattern. Last year we reviewed all the 71 cases reported as RS up to 2011, and questioned ...
متن کاملBrugada syndrome--an update.
A diagnostic triad characterizes Brugada syndrome. It consists of a right bundle branch block, ST-segment elevation in leads V1-V3 and sudden cardiac death (SCD). Approximately 50% of patients with Brugada syndrome noted to have familial occurrence, this suggests a genetic component of the disease. Mutations in gene SCN5A, an encoder for human cardiac sodium channel on chromosome 3p21, causes B...
متن کاملPOEMS SYNDROME: an Update
POEMS syndrome is a rare, chronic and disabling condition. The causes of this condition remain unknown; however, chronic overproduction of proinflammatory cytokines appears to be a major contributor. Early diagnosis is essential to start treatment before the clinical state of the patient becomes compromised. A complete evaluation of the disease at its onset is critical to the treatment decision...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Epilepsia
سال: 2006
ISSN: 0013-9580,1528-1167
DOI: 10.1111/j.1528-1167.2006.00704.x