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New CACNA1A deletions are associated to migraine phenotypes.
Grieco GS, Gagliardi S, Ricca I, Pansarasa O, Neri M, Gualandi F, Nappi G, Ferlini A, Cereda C. Grieco GS, et al. J Headache Pain. 2018 Aug 30;19(1):75. doi: 10.1186/s10194-018-0891-x. J Headache Pain. 2018. PMID: 30167989 Free PMC article.
Palmoplantar keratoderma and Charcot-Marie-Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole-exome sequencing.
Gagliardi S, Ricca I, Ferrarini A, Valente M, Grieco GS, Piccolo G, Alfonsi E, Delledonne M, Cereda C. Gagliardi S, et al. Among authors: grieco gs. Br J Dermatol. 2017 Jul;177(1):284-286. doi: 10.1111/bjd.15066. Epub 2017 Jun 14. Br J Dermatol. 2017. PMID: 27639257 No abstract available.
Novel CLN3 mutation causing autophagic vacuolar myopathy.
Cortese A, Tucci A, Piccolo G, Galimberti CA, Fratta P, Marchioni E, Grampa G, Cereda C, Grieco G, Ricca I, Pittman A, Ciscato P, Napoli L, Lucchini V, Ripolone M, Violano R, Fagiolari G, Mole SE, Hardy J, Moglia A, Moggio M. Cortese A, et al. Neurology. 2014 Jun 10;82(23):2072-6. doi: 10.1212/WNL.0000000000000490. Epub 2014 May 14. Neurology. 2014. PMID: 24827497 Free PMC article.
A new GLUT-1 mutation in a family with glucose transporter 1 deficiency syndrome.
Gagliardi S, Davin A, Ricca I, Grieco GS, Zangaglia R, Pierelli F, Ghiroldi A, Pacchetti C, Casali C, Cereda C. Gagliardi S, et al. Among authors: grieco gs. Mov Disord. 2012 May;27(6):804-5. doi: 10.1002/mds.24966. Epub 2012 Mar 21. Mov Disord. 2012. PMID: 22437877 No abstract available.
48 results