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30 Publications

2019 | Journal Article | IST-REx-ID: 7149
Avagliano L, Parenti I, Grazioli P, et al. Chromatinopathies: A focus on Cornelia de Lange syndrome. Clinical Genetics. 2019. doi:10.1111/cge.13674
View | DOI | PubMed | Europe PMC
 
2018 | Thesis | IST-REx-ID: 395   OA
Tarlungeanu D-C. The Branched Chain Amino Acids in Autism Spectrum Disorders . IST Austria; 2018. doi:10.15479/AT:ISTA:th_992
View | Files available | DOI
 
2018 | Journal Article | IST-REx-ID: 456
Novarino G. Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine. 2018;10(423). doi:10.1126/scitranslmed.aar7514
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2018 | Journal Article | IST-REx-ID: 691   OA
Marin Valencia I, Novarino G, Johansen A, et al. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics. 2018;55(1):48-54. doi:10.1136/jmedgenet-2017-104627
View | DOI | Download (ext.) | PubMed | Europe PMC
 
2018 | Journal Article | IST-REx-ID: 546
Sacco R, Cacci E, Novarino G. Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology. 2018;48(2):131-138. doi:10.1016/j.conb.2017.12.005
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