Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Prabowo Avanita S"'
Autor:
Prabowo Avanita S, Iyer Anand M, Anink Jasper J, Spliet Wim GM, van Rijen Peter C, Aronica Eleonora
Publikováno v:
Journal of Neuroinflammation, Vol 10, Iss 1, p 12 (2013)
Abstract Purpose The expression of the major histocompatibility complex class I (MHC-I) in the brain has received considerable interest not only because of its fundamental role in the immune system, but also for its non-immune functions in the contex
Externí odkaz:
https://doaj.org/article/d24d3e8ef5414e2fb81d7a290f566b82
Autor:
Prabowo, Avanita S.1, Thuijl, Hinke Foka2,3, Scheinin, Ilari3,4, Sie, Daoud3, Essen, Hendrik F.3, Iyer, Anand M.1, Spliet, Wim G.M.5, Ferrier, Cyrille H.6,7, Rijen, Peter C.6, Veersema, Tim J.6,8, Thom, Maria9, Schouten‐van Meeteren, Annetteke Y.N.10, Reijneveld, Jaap C.2,11, Ylstra, Bauke3, Wesseling, Pieter3,12, Aronica, Eleonora1,13,14
Publikováno v:
Neuropathology & Applied Neurobiology. Oct2015, Vol. 41 Issue 6, p743-755. 13p.
Autor:
Scholl, Theresa, Mühlebner, Angelika, Ricken, Gerda, Gruber, Victoria, Fabing, Anna, Samueli, Sharon, Gröppel, Gudrun, Dorfer, Christian, Czech, Thomas, Hainfellner, Johannes A., Prabowo, Avanita S., Reinten, Roy J., Hoogendijk, Lisette, Anink, Jasper J., Aronica, Eleonora, Feucht, Martha
Publikováno v:
Brain pathology (Zurich, Switzerland), 27(6), 770-780. Wiley-Blackwell
Conventional antiepileptic drugs suppress the excessive firing of neurons during seizures. In drug-resistant patients, treatment failure indicates an alternative important epileptogenic trigger. Two epilepsy-associated pathologies show myelin deficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::f69ad1a7e1259b13bc35ddc67e65d09c
https://pure.amc.nl/en/publications/impaired-oligodendroglial-turnover-is-associated-with-myelin-pathology-in-focal-cortical-dysplasia-and-tuberous-sclerosis-complex(8e891703-f73b-4a83-95f4-a17074893ec8).html
https://pure.amc.nl/en/publications/impaired-oligodendroglial-turnover-is-associated-with-myelin-pathology-in-focal-cortical-dysplasia-and-tuberous-sclerosis-complex(8e891703-f73b-4a83-95f4-a17074893ec8).html
Autor:
Prabowo, Avanita S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::0477c171bb4555941aa15c12fe0956b7
https://pure.amc.nl/en/publications/molecular-features-of-longterm-epilepsyassociated-tumors-focus-on-glioneuronal-tumors(9b8503cc-4153-4418-a039-6bb557be4f86).html
https://pure.amc.nl/en/publications/molecular-features-of-longterm-epilepsyassociated-tumors-focus-on-glioneuronal-tumors(9b8503cc-4153-4418-a039-6bb557be4f86).html
Autor:
Prabowo, Avanita S., Iyer, Anand M., Veersema, Tim J., Anink, Jasper J., Schouten-van Meeteren, Antoinette Y. N., Spliet, Wim G. M., van Rijen, Pieter C., Ferrier, Cyrille H., Capper, David, Thom, Maria, Aronica, Eleonora
Publikováno v:
Brain Pathol
Brain pathology (Zurich, Switzerland), 24(1), 52-66. Wiley-Blackwell
Brain pathology (Zurich, Switzerland), 24(1), 52-66. Wiley-Blackwell
BRAF V600E mutations have been recently reported in glioneuronal tumors (GNTs). To evaluate the expression of the BRAF V600E mutated protein and its association with activation of the mammalian target of rapamycin (mTOR) pathway, immunophenotype and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b9fed277d0db23b6033e026a2d2d27ce
https://europepmc.org/articles/PMC8029322/
https://europepmc.org/articles/PMC8029322/
Autor:
Prabowo, Avanita S., Anink, Jasper J., Lammens, Martin, Nellist, Mark, van den Ouweland, Ans M. W., Adle-Biassette, Homa, Sarnat, Harvey B., Flores-Sarnat, Laura, Crino, Peter B., Aronica, Eleonora
Publikováno v:
Brain Pathology, 23(1), 45-59. Wiley-Blackwell
Brain Pathology; Vol 23
Brain pathology (Zurich, Switzerland), 23(1), 45-59. Wiley-Blackwell
Brain Pathology, 23, 45-59
Brain Pathology, 23, 1, pp. 45-59
Brain Pathology
Brain Pathology; Vol 23
Brain pathology (Zurich, Switzerland), 23(1), 45-59. Wiley-Blackwell
Brain Pathology, 23, 45-59
Brain Pathology, 23, 1, pp. 45-59
Brain Pathology
Item does not contain fulltext Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutations in either the TSC1 or TSC2 genes and characterized by developmental brain abnormalities. We defined the spectrum of brain abnormalit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1249bd400fd830fffd972267b235ba2f
https://pure.eur.nl/en/publications/0ed62f7b-8e24-431f-9ed6-9437741c96e5
https://pure.eur.nl/en/publications/0ed62f7b-8e24-431f-9ed6-9437741c96e5
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Akademický článek
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Autor:
Prabowo, Avanita S., Venkatachalam, Ramprasath, Kamping, Eveline, Ligtenberg, Marjolijn J., Hoogerbrugge, Nicoline, Geurts van Kessel, Ad, Kuiper, Roland P.
Publikováno v:
In Cancer Genetics and Cytogenetics 2010 203(1):47-47