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30 Publications

2019 | Journal Article | IST-REx-ID: 7149
Avagliano L, Parenti I, Grazioli P, Di Fede E, Parodi C, Mariani M, Kaiser FJ, Selicorni A, Gervasini C, Massa V. 2019. Chromatinopathies: A focus on Cornelia de Lange syndrome. Clinical Genetics.
View | DOI | PubMed | Europe PMC
 
2018 | Thesis | IST-REx-ID: 395   OA
Tarlungeanu D-C. 2018. The branched chain amino acids in autism spectrum disorders , IST Austria, 88p.
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2018 | Journal Article | IST-REx-ID: 456
Novarino G. 2018. Zika-associated microcephaly: Reduce the stress and race for the treatment. Science Translational Medicine. 10(423).
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2018 | Journal Article | IST-REx-ID: 691   OA
Marin Valencia I, Novarino G, Johansen A, Rosti B, Issa M, Musaev D, Bhat G, Scott E, Silhavy J, Stanley V, Rosti R, Gleeson J, Imam F, Zaki M, Gleeson J. 2018. A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features. Journal of Medical Genetics. 55(1), 48–54.
View | DOI | Download (ext.) | PubMed | Europe PMC
 
2018 | Journal Article | IST-REx-ID: 546
Sacco R, Cacci E, Novarino G. 2018. Neural stem cells in neuropsychiatric disorders. Current Opinion in Neurobiology. 48(2), 131–138.
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