Neri G - Search Results

1

Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome.

Giovannini S, Frattini D, Scarano A, Fusco C, Bertani G, Della Giustina E, Martinelli P, Orteschi D, Zollino M, Neri G, Gobbi G. Giovannini S, et al. Among authors: neri g. Epileptic Disord. 2010 Sep;12(3):222-7. doi: 10.1684/epd.2010.0324. Epub 2010 Jul 19. Epileptic Disord. 2010. PMID: 20643614 Free article.

2

Epilepsy in ring 14 syndrome: a clinical and EEG study of 22 patients.

Giovannini S, Marangio L, Fusco C, Scarano A, Frattini D, Della Giustina E, Zollino M, Neri G, Gobbi G. Giovannini S, et al. Among authors: neri g. Epilepsia. 2013 Dec;54(12):2204-13. doi: 10.1111/epi.12393. Epub 2013 Oct 1. Epilepsia. 2013. PMID: 24116895 Free article.

3

The ring 14 syndrome: clinical and molecular definition.

Zollino M, Seminara L, Orteschi D, Gobbi G, Giovannini S, Della Giustina E, Frattini D, Scarano A, Neri G. Zollino M, et al. Among authors: neri g. Am J Med Genet A. 2009 Jun;149A(6):1116-24. doi: 10.1002/ajmg.a.32831. Am J Med Genet A. 2009. PMID: 19441122

4

Phenotypic map in ring 14 syndrome.

Zollino M, Orteschi D, Neri G. Zollino M, et al. Among authors: neri g. Am J Med Genet A. 2010 Jan;152A(1):237. doi: 10.1002/ajmg.a.33169. Am J Med Genet A. 2010. PMID: 20034092 No abstract available.

5

The ring 14 syndrome.

Zollino M, Ponzi E, Gobbi G, Neri G. Zollino M, et al. Among authors: neri g. Eur J Med Genet. 2012 May;55(5):374-80. doi: 10.1016/j.ejmg.2012.03.009. Epub 2012 Apr 14. Eur J Med Genet. 2012. PMID: 22564756 Review.

6

"Minimal" holoprosencephaly in a 14q deletion syndrome patient.

Della Giustina E, Iodice A, Spagnoli C, Giovannini S, Frattini D, Fusco C, Gobbi G, Zollino M, Neri G. Della Giustina E, et al. Among authors: neri g. Am J Med Genet A. 2017 Dec;173(12):3216-3220. doi: 10.1002/ajmg.a.38378. Am J Med Genet A. 2017. PMID: 29136354

7

Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndrome.

Zollino M, Gurrieri F, Orteschi D, Marangi G, Leuzzi V, Neri G. Zollino M, et al. Among authors: neri g. Eur J Hum Genet. 2011 Feb;19(2):239-42. doi: 10.1038/ejhg.2010.172. Epub 2010 Dec 1. Eur J Hum Genet. 2011. PMID: 21119708 Free PMC article.

8

Partial deletion of chromosome 12q is not usually associated with CFC syndrome.

Zollino M, Neri G. Zollino M, et al. Among authors: neri g. Am J Med Genet. 2000 Nov 27;95(3):296. Am J Med Genet. 2000. PMID: 11102944 No abstract available.

9

Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.

Tabolacci E, Pomponi MG, Remondini L, Pietrobono R, Orteschi D, Nobile V, Pucci C, Musto E, Pane M, Mercuri EM, Neri G, Genuardi M, Chiurazzi P, Zollino M. Tabolacci E, et al. Among authors: neri g. Genes (Basel). 2021 Nov 27;12(12):1909. doi: 10.3390/genes12121909. Genes (Basel). 2021. PMID: 34946857 Free PMC article.

10

Chromosome 14 deletions, rings, and epilepsy genes: A riddle wrapped in a mystery inside an enigma.

Vaisfeld A, Spartano S, Gobbi G, Vezzani A, Neri G. Vaisfeld A, et al. Among authors: neri g. Epilepsia. 2021 Jan;62(1):25-40. doi: 10.1111/epi.16754. Epub 2020 Nov 17. Epilepsia. 2021. PMID: 33205446 Review.

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