Glut1 Treff i utvalgte kilder: [Skjul boksen]
  1. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/686/differentials
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    ... in 60% of patients Paroxysmal exercise-induced dyskinesia GLUT1 History Exam 1st investigation Other investigations generalised epilepsy ( ... in 60% of patients Paroxysmal exercise-induced dyskinesia GLUT1 History Exam 1st investigation Other investigations generalised epilepsy ( ...
  2. nokc-helsebiblioteket-collection
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    https://www.helsebiblioteket.no/...lepsianfall-med-absenser-hos-barn
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    ... epilepsi med absens skyldes en genetisk lidelse kalt GLUT1- mangelsykdom. Sykdommen påvirker transporten av glukose til hjernen. ... epileptiske anfall. Barnets lege kan anbefale testing for GLUT1-mangelsykdom dersom barnet er under 4 år eller ...
  3. nokc-helsebiblioteket-collection
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    https://www.helsebiblioteket.no/.../vaskulære-lesjoner
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    ... receptor II, merosin og Lewis Y antigen) og GLUT1-antigen. Disse antigenene er ikke til stede på ... ikke i regresjon. Både RICH og NICH er GLUT1-negative. Tufted angiomas (TA) Dette er en sjelden ...
  4. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/115/pdf/115.pdf
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    ... epilepsy have been attributed to mutations in the GLUT1 glucose transporter. [ 28] BASICS Clas sifi cation International ... absence epilepsy to evaluate for glucose transporter 1 (GLUT1) deficiency. [ 28] [ 32] Genetic testing No commercially available ...
  5. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/1041/pdf/1041.pdf
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    ... distinguished histologically by the absence of staining with GLUT1, an endothelial cell marker that is present in ... fatty tissue. [ 42] [ 44] Haemangiomas uniquely stain for GLUT1, an erythrocyte-type glucose transporter present in infantile ...
  6. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/1041/differentials
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    ... nlm.nih.gov/pubmed/15018449?tool=bestpractice.com GLUT1 staining negative. [45] North PE, Waner M, Mizeracki A, et al. GLUT1: a newly discovered immunohistochemical marker for juvenile hemangioma. ...
  7. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/115/pdf/115.pdf
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    ... epilepsy have been attributed to mutations in the GLUT1 glucose transporter. [ 28] BASICS Clas sifi cation International ... absence epilepsy to evaluate for glucose transporter 1 (GLUT1) deficiency. [ 28] [ 32] Genetic testing No commercially available ...
  8. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/1041/pdf/1041.pdf
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    ... distinguished histologically by the absence of staining with GLUT1, an endothelial cell marker that is present in ... fatty tissue. [ 42] [ 44] Hemangiomas uniquely stain for GLUT1, an erythrocyte-type glucose transporter present in infantile ...
  9. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/686/pdf/686.pdf
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    ... impaired glucose transporter of the blood-brain barrier GLUT1. [ 12] • Infantile parkinsonism-dystonia associated with an autosomal- ... for mitochondrial encephalomyopathies • Serum and CSF glucose for GLUT1 • CSF studies of neurotransmitters in infantile parkinsonism-dystonia. ...
  10. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/115/diagnosis-approach
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    ... absence epilepsy to evaluate for glucose transporter 1 (GLUT1) deficiency. [28] Mullen SA, Suls A, De Jonghe ... variable onset are a key feature of familial GLUT1 deficiency. Neurology. 2010 Aug 3;75(5):432- ...
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