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Articles, 3 records found
Articles 3 records found  
1.
21 p, 4.1 MB Embedding MRI information into MRSI data source extraction improves brain tumour delineation in animal models / Ortega-Martorell, Sandra (Liverpool John Moores University. Department of Applied Mathematics) ; Candiota Silveira, Ana Paula (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular) ; Thomson, Ryan (Liverpool John Moores University. Department of Applied Mathematics) ; Riley, Patrick (Liverpool John Moores University. Department of Applied Mathematics) ; Julià Sapé, Ma. Margarita (Universitat Autònoma de Barcelona. Departament de Bioquímica i de Biologia Molecular) ; Olier, Iván (Liverpool John Moores University. Department of Applied Mathematics) ; Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí"
Glioblastoma is the most frequent malignant intra-cranial tumour. Magnetic resonance imaging is the modality of choice in diagnosis, aggressiveness assessment, and follow-up. However, there are examples where it lacks diagnostic accuracy. [...]
2019 - 10.1371/journal.pone.0220809
PloS one, Vol. 14, Núm. 8 (2019) , art. e0220809  
Detailed record - Creative Commons
2.
9 p, 2.9 MB GNAO1 encephalopathy : further delineation of a severe neurodevelopmental syndrome affecting females / Marcé-Grau, Anna (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Dalton, James A. R.. (Universitat Autònoma de Barcelona. Institut de Neurociències) ; López-Pisón, Javier (Hospital Universitario Miguel Servet (Saragossa)) ; García-Jiménez, María Concepción (Hospital Universitario Miguel Servet (Saragossa)) ; Monge-Galindo, Lorena (Hospital Universitario Miguel Servet (Saragossa)) ; Cuenca-León, Ester (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Giraldo, Jesús (Universitat Autònoma de Barcelona. Institut de Neurociències) ; Macaya Ruiz, Alfons (Hospital Universitari Vall d'Hebron)
De novo heterozygous mutations in the GNAO1 gene, encoding the Gα o subunit of G-proteins, are the cause of a severe neurodevelopmental disorder, featuring early infantile seizures, profound cognitive dysfunction and, occasionally, movement disorder (early infantile epileptic encephalopathy-17). [...]
2016 - 10.1186/s13023-016-0416-0
Orphanet Journal of Rare Diseases, Vol. 11 (april 2016)  
Detailed record - Creative Commons
3.
1 p, 145.2 KB Delineation / Crews, Judson
1968
Wormwood Review, Vol. 8 Núm. 3, Issue 31 (1968) , p. 31-32  
Detailed record -

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