Glucose transporter-1 deficiency syndrome: From cerebrospinal fluid to clinical practice.

Contains fulltext : MMUBN000001_938013866.pdf (publisher's version ) (Closed access)Radboud Universiteit Nijmegen, 27 juni 2014Promotores : Willemsen, M.A.A.P., Engelen, B.G.M. van Co-promotores : Verbeek, M.M., Scheffer, H

Lactate and its many faces

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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding.

Contains fulltext : 218874.pdf (Publisher’s version ) (Closed access)1 januari 202

Chronic herpes simplex virus encephalitis in childhood.

Contains fulltext : 50896.pdf (publisher's version ) (Closed access)Although herpes simplex virus is a major cause of acute encephalitis in childhood, chronic herpes simplex virus encephalitis has only rarely been reported. This report presents a case of chronic herpes simplex virus encephalitis in a 6-year-old female. Diagnosis was based on the detection of herpes simplex virus deoxyribonucleic acid by polymerase chain reaction in combination with the cerebrospinal fluid/serum ratio of herpes simplex virus-specific immunoglobulin G, the presence of herpes simplex virus-specific oligoclonal immunoglobulin G bands in cerebrospinal fluid, and calcifications in the temporal regions found on cerebral computed tomographic scan. Prolonged antiviral therapy was beneficial to later mental development

Hourly analysis of cerebrospinal fluid glucose shows large diurnal fluctuations

Item does not contain fulltextCerebrospinal fluid analysis is important in the diagnostics of many neurological disorders. Since the influence of food intake on the cerebrospinal fluid glucose concentration and the cerebrospinal fluid/plasma glucose ratio is largely unknown, we studied fluctuations in these parameters in healthy adult volunteers during a period of 36 h. Our observations show large physiological fluctuations of cerebrospinal fluid glucose and the cerebrospinal fluid/plasma glucose ratio, and their relation to food intake. These findings provide novel insights into the physiology of cerebral processes dependent on glucose levels such as energy formation (e.g. glycolysis), enzymatic reactions (e.g. glycosylation), and non-enzymatic reactions (e.g. advanced endproduct glycation)

Rituximab and intravenous immunoglobulins for relapsing postinfectious opsoclonus-myoclonus syndrome.

Contains fulltext : 71126.pdf (publisher's version ) (Closed access)We describe 2 children with postinfectious opsoclonus-myoclonus syndrome. Although the patients initially responded to monotherapy with methylprednisolone, intravenous immunoglobulins, or rituximab, they manifested persistent neurologic deficits and relapsing signs. Treatment with rituximab in combination with intravenous immunoglobulin, however, resulted in significant longterm clinical improvement

GLUT1 deficiëntie syndroom.

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De ontwikkelingsstoornissen ADHD en autisme in de huisartspraktijk

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Head circumference in glucose transporter 1 deficiency syndrome: Normal for individuals, abnormal as a group

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Ptosis as a feature of late-onset glycogenosis type II.

Contains fulltext : 50171.pdf (publisher's version ) (Closed access