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Showing 1 to 1 of 1 for “"Settore MEDS-20/B - Neuropsichiatria infantile"”.

  1. EXPANSION OF CLINICAL PHENOTYPE AND USE OF KETOGENIC DIET IN RARE GENETIC CONDITIONS: GLUCOSE TRANSPORTER TYPE 1 DEFICIENCY SYNDROME AND SCN8A-RELATED DISORDERS

    … episodes were observed in approximately 20% of patients, especially in post-pubertal females, including one documented case of ischemic stroke. Therefore, attention should be paid to the occurrence of acute neurological symptoms in patients with GLUT1-DS, and conversely, this syndrome …

    milano Repository record for EXPANSION OF CLINICAL PHENOTYPE AND USE OF KETOGENIC DIET IN RARE GENETIC CONDITIONS: GLUCOSE TRANSPORTER TYPE 1 DEFICIENCY SYNDROME AND SCN8A-RELATED DISORDERS (opens in a new tab)