Galli J - Search Results

1

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: galli j. Neuropediatrics. 2018 Feb;49(1):26-34. doi: 10.1055/s-0037-1607216. Epub 2017 Oct 9. Neuropediatrics. 2018. PMID: 28992644

2

Neuropsychiatric aid in children born to patients with rheumatic diseases.

Bomba M, Galli J, Nacinovich R, Ceribelli A, Motta M, Lojacono A, Fazzi E, Tincani A. Bomba M, et al. Among authors: galli j. Clin Exp Rheumatol. 2010 Sep-Oct;28(5):767-73. Epub 2010 Oct 22. Clin Exp Rheumatol. 2010. PMID: 20822715 Review.

3

The Aicardi-Goutières syndrome. Molecular and clinical features of RNAse deficiency and microRNA overload.

Pulliero A, Fazzi E, Cartiglia C, Orcesi S, Balottin U, Uggetti C, La Piana R, Olivieri I, Galli J, Izzotti A. Pulliero A, et al. Among authors: galli j. Mutat Res. 2011 Dec 1;717(1-2):99-108. doi: 10.1016/j.mrfmmm.2011.03.018. Epub 2011 Apr 15. Mutat Res. 2011. PMID: 21524657

4

Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients.

Briguglio M, Pinelli L, Giordano L, Ferraris A, Germanò E, Micheletti S, Severino M, Bernardini L, Loddo S, Tortorella G, Ormitti F, Gasparotti R; CBCD Study Group; Rossi A, Valente EM. Briguglio M, et al. Orphanet J Rare Dis. 2011 Jun 8;6:36. doi: 10.1186/1750-1172-6-36. Orphanet J Rare Dis. 2011. PMID: 21651769 Free PMC article.

5

Neuro-ophthalmological disorders in cerebral palsy: ophthalmological, oculomotor, and visual aspects.

Fazzi E, Signorini SG, LA Piana R, Bertone C, Misefari W, Galli J, Balottin U, Bianchi PE. Fazzi E, et al. Among authors: galli j. Dev Med Child Neurol. 2012 Aug;54(8):730-6. doi: 10.1111/j.1469-8749.2012.04324.x. Epub 2012 Jun 19. Dev Med Child Neurol. 2012. PMID: 22712803 Free article.

6

Aicardi-Goutieres syndrome, a rare neurological disease in children: a new autoimmune disorder?

Fazzi E, Cattalini M, Orcesi S, Tincani A, Andreoli L, Balottin U, De Simone M, Fredi M, Facchetti F, Galli J, Giliani S, Izzotti A, Meini A, Olivieri I, Plebani A. Fazzi E, et al. Among authors: galli j. Autoimmun Rev. 2013 Feb;12(4):506-9. doi: 10.1016/j.autrev.2012.08.012. Epub 2012 Aug 24. Autoimmun Rev. 2013. PMID: 22940555 Review.

7

Dysregulation of the immune system in Aicardi-Goutières syndrome: another example in a TREX1-mutated patient.

Olivieri I, Cattalini M, Tonduti D, La Piana R, Uggetti C, Galli J, Meini A, Tincani A, Moratto D, Fazzi E, Balottin U, Orcesi S. Olivieri I, et al. Among authors: galli j. Lupus. 2013 Sep;22(10):1064-9. doi: 10.1177/0961203313498800. Epub 2013 Aug 5. Lupus. 2013. PMID: 23918923

8

Exploring Autoimmunity in a Cohort of Children with Genetically Confirmed Aicardi-Goutières Syndrome.

Cattalini M, Galli J, Andreoli L, Olivieri I, Ariaudo G, Fredi M; IAGSA study group; Orcesi S, Tincani A, Fazzi E. Cattalini M, et al. Among authors: galli j. J Clin Immunol. 2016 Oct;36(7):693-9. doi: 10.1007/s10875-016-0325-y. Epub 2016 Aug 18. J Clin Immunol. 2016. PMID: 27539236

9

Dissection of partial 21q monosomy in different phenotypes: clinical and molecular characterization of five cases and review of the literature.

Errichiello E, Novara F, Cremante A, Verri A, Galli J, Fazzi E, Bellotti D, Losa L, Cisternino M, Zuffardi O. Errichiello E, et al. Among authors: galli j. Mol Cytogenet. 2016 Feb 24;9(1):21. doi: 10.1186/s13039-016-0230-3. eCollection 2016. Mol Cytogenet. 2016. PMID: 27625702 Free PMC article.

10

Neurodevelopmental profile in Angelman syndrome: more than low intelligence quotient.

Micheletti S, Palestra F, Martelli P, Accorsi P, Galli J, Giordano L, Trebeschi V, Fazzi E. Micheletti S, et al. Among authors: galli j. Ital J Pediatr. 2016 Oct 21;42(1):91. doi: 10.1186/s13052-016-0301-4. Ital J Pediatr. 2016. PMID: 27769316 Free PMC article.

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