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Year Number of Results
2008 1
2009 1
2013 2
2014 4
2015 4
2016 3
2017 1
2018 3
2019 1
2020 2
2021 2
2022 3
2024 2

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Page 1
Neurodevelopmental Profile in Children Affected by Ocular Albinism.
Galli J, Loi E, Morandi A, Scaglioni V, Rossi A, Molinaro A, Pasini N, Semeraro F, Ruberto G, Fazzi E. Galli J, et al. Among authors: molinaro a. Neuropediatrics. 2022 Feb;53(1):7-14. doi: 10.1055/s-0041-1732430. Epub 2021 Jul 29. Neuropediatrics. 2022. PMID: 34327695
Neurovisual Assessment in Children with Ataxia Telangiectasia.
Iodice A, Galli J, Molinaro A, Franzoni A, Micheli R, Pinelli L, Plebani A, Soresina A, Fazzi E. Iodice A, et al. Among authors: molinaro a. Neuropediatrics. 2018 Feb;49(1):26-34. doi: 10.1055/s-0037-1607216. Epub 2017 Oct 9. Neuropediatrics. 2018. PMID: 28992644
Positive effect of erythrocyte-delivered dexamethasone in ataxia-telangiectasia.
Leuzzi V, Micheli R, D'Agnano D, Molinaro A, Venturi T, Plebani A, Soresina A, Marini M, Ferremi Leali P, Quinti I, Pietrogrande MC, Finocchi A, Fazzi E, Chessa L, Magnani M. Leuzzi V, et al. Among authors: molinaro a. Neurol Neuroimmunol Neuroinflamm. 2015 Apr 9;2(3):e98. doi: 10.1212/NXI.0000000000000098. eCollection 2015 Jun. Neurol Neuroimmunol Neuroinflamm. 2015. PMID: 25884015 Free PMC article.
Neurodevelopmental profile in children born to mothers affected by systemic sclerosis.
Galli J, Loi E, Lazzaroni MG, Molinaro A, Andreoli L, Bendoni M, Moschetti L, Pedretti E, Visconti LM, Airò P, Franceschini F, Tincani A, Fazzi E. Galli J, et al. Among authors: molinaro a. Early Hum Dev. 2024 Apr;191:105988. doi: 10.1016/j.earlhumdev.2024.105988. Epub 2024 Mar 19. Early Hum Dev. 2024. PMID: 38531240 Free article.
Legius Syndrome: two novel mutations in the SPRED1 gene.
Bianchi M, Saletti V, Micheli R, Esposito S, Molinaro A, Gagliardi S, Orcesi S, Cereda C. Bianchi M, et al. Among authors: molinaro a. Hum Genome Var. 2015 Dec 3;2:15051. doi: 10.1038/hgv.2015.51. eCollection 2015. Hum Genome Var. 2015. PMID: 27081556 Free PMC article.
22 results