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024 7 _ |2 pmid
|a pmid:22161228
024 7 _ |2 DOI
|a 10.1055/s-0031-1281851
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|a WOS:000299650200015
037 _ _ |a PreJuSER-19204
041 _ _ |a ger
082 _ _ |a 610
084 _ _ |2 WoS
|a Clinical Neurology
084 _ _ |2 WoS
|a Psychiatry
100 1 _ |a Galldiks, N.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB73298
245 _ _ |a Anwendung der Aminosäure-PET in der Diagnostik und Therapie von zerebralen Gliomen (Use of amino acid PET in the diagnostic and treatment management of cerebral gliomas)
260 _ _ |a Stuttgart [u.a.]
|b Thieme
|c 2012
300 _ _ |a 17 - 23
336 7 _ |a Journal Article
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336 7 _ |a article
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440 _ 0 |a Fortschritte der Neurologie Psychiatrie
|x 0720-4299
|0 18781
|y 1
|v 80
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Structural as well as functional imaging methods are of special importance in neurooncology. Improvements of radionuclide and magnetic resonance-based imaging modalities over the past decade have enabled clinicians to non-invasively assess the dynamics of disease-specific processes at the molecular level in patients with malignant gliomas. To date, a range of complementary imaging parameters have been established in the diagnostic work-up of patients with brain tumours. Magnetic resonance imaging (MRI) provides morphological information as well as functional information such as vascular permeability, cell density, tumour perfusion, and metabolic information by using magnetic resonance spectroscopy. The use of radiolabelled amino acids for positron emission tomography (PET) allows a better delineation of tumour margins and improves targeting of biopsy and radiotherapy, and planning surgery. In addition, amino acid imaging appears useful in distinguishing tumour recurrence from non-specific post-therapeutic scar tissue, in predicting prognosis in low-grade gliomas, and in monitoring metabolic response during treatment. Taken together, MRI and PET provide complementary information about tumour biology and activity, thereby resulting in an improved understanding of the kinetics of tumour growth and therefore allow new insights into the pathophysiology of malignant brain tumours. However, multimodal imaging studies comparing the value of amino acid PET and functional methods of MRI (e. g., perfusion and diffusion weighted imaging) are needed. From these studies, surrogate MRI and PET imaging techniques need to be derived to gain complementary structural and functional information of brain tumours that can be placed into common clinical practice which will optimise the clinical management of patients with malignant gliomas.
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|a Funktion und Dysfunktion des Nervensystems (FUEK409)
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588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Amino Acids: diagnostic use
650 _ 2 |2 MeSH
|a Biopsy
650 _ 2 |2 MeSH
|a Brain: pathology
650 _ 2 |2 MeSH
|a Brain: radionuclide imaging
650 _ 2 |2 MeSH
|a Brain Neoplasms: pathology
650 _ 2 |2 MeSH
|a Brain Neoplasms: radionuclide imaging
650 _ 2 |2 MeSH
|a Brain Neoplasms: therapy
650 _ 2 |2 MeSH
|a Combined Modality Therapy
650 _ 2 |2 MeSH
|a Glioma: pathology
650 _ 2 |2 MeSH
|a Glioma: radionuclide imaging
650 _ 2 |2 MeSH
|a Glioma: therapy
650 _ 2 |2 MeSH
|a Humans
650 _ 2 |2 MeSH
|a Magnetic Resonance Imaging
650 _ 2 |2 MeSH
|a Neoplasm Recurrence, Local
650 _ 2 |2 MeSH
|a Neurosurgical Procedures
650 _ 2 |2 MeSH
|a Patient Care Planning
650 _ 2 |2 MeSH
|a Positron-Emission Tomography: methods
650 _ 2 |2 MeSH
|a Prognosis
650 _ 2 |2 MeSH
|a Radiopharmaceuticals: diagnostic use
650 _ 7 |0 0
|2 NLM Chemicals
|a Amino Acids
650 _ 7 |0 0
|2 NLM Chemicals
|a Radiopharmaceuticals
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a C-11-methyl-L-methionine
653 2 0 |2 Author
|a O-(2-[F-18]-fluoroethyl)-L-tyrosine
653 2 0 |2 Author
|a metabolic imaging
700 1 _ |a Langen, K.-J.
|b 1
|u FZJ
|0 P:(DE-Juel1)131777
773 _ _ |a 10.1055/s-0031-1281851
|g Vol. 80, p. 17 - 23
|p 17 - 23
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|0 PERI:(DE-600)2037701-0
|t Fortschritte der Neurologie, Psychiatrie
|v 80
|y 2012
|x 0720-4299
856 7 _ |u http://dx.doi.org/10.1055/s-0031-1281851
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