Search Results - "Sandvig, I"
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1
15 year old Norwegian boy with MOG-antibody positive demyelinating disease
Published in European journal of paediatric neurology (01-06-2017)Get full text
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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder
Published in Brain (London, England : 1878) (01-03-2010)“…Glucose transporter-1 deficiency syndrome is caused by mutations in the SLC2A1 gene in the majority of patients and results in impaired glucose transport into…”
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Clinical guidance for diagnosis and management of suspected Pediatric Acute‐onset Neuropsychiatric Syndrome in the Nordic countries
Published in Acta Paediatrica (01-12-2021)“…Pediatric acute‐onset neuropsychiatric syndrome is a clinical concept used to describe a subgroup of children with sudden onset of psychiatric and somatic…”
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Authors' reply regarding “On diagnosing and treating PANS/PANDAS: Questions from a patient support group”
Published in Acta Paediatrica (01-12-2021)Get full text
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Multiple sclerosis in children and adolescents. An important differential diagnosis of acute neurological disease
Published in European journal of paediatric neurology (01-03-2015)“…Abstract Aim Multiple sclerosis (MS) has traditionally been considered a disease of adults. However, in recent years, there have been numerous reports about…”
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Infantile spasms
Published in Tidsskrift for den Norske Lægeforening (11-08-2005)“…Infantile spasms are an epileptic manifestation typical of infancy. The spasms may be associated with a wide spectrum of brain abnormalities and diseases, but…”
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