Anichini C - Search Results

1

Antioxidant strategies in genetic syndromes with high neoplastic risk in infant age.

Anichini C, Lotti F, Longini M, Felici C, Proietti F, Buonocore G. Anichini C, et al. Tumori. 2014 Nov-Dec;100(6):590-9. doi: 10.1700/1778.19256. Tumori. 2014. PMID: 25688491 Review.

2

Beckwith-Wiedemann syndrome: potassium ascorbate with ribose therapy in a syndrome with high neoplastic risk.

Anichini C, Lo Rizzo C, Longini M, Paoli G, di Bartolo RM, Proietti F, Buonocore G. Anichini C, et al. Anticancer Res. 2011 Nov;31(11):3973-6. Anticancer Res. 2011. PMID: 22110229

3

Antioxidant effects of potassium ascorbate with ribose in costello syndrome.

Anichini C, Lotti F, Pietrini A, Lo Rizzo C, Longini M, Proietti F, Felici C, Buonocore G. Anichini C, et al. Anticancer Res. 2013 Feb;33(2):691-5. Anticancer Res. 2013. PMID: 23393369

4

Antioxidant effects of potassium ascorbate with ribose therapy in a case with Prader Willi Syndrome.

Anichini C, Lotti F, Longini M, Proietti F, Felici C, Perrone S, Buonocore G. Anichini C, et al. Dis Markers. 2012;33(4):179-83. doi: 10.3233/DMA-2012-0922. Dis Markers. 2012. PMID: 22960339 Free PMC article.

5

Photoparoxysmal responses in children with chromosomal aberrations.

Grosso S, Pucci L, Bartalini G, Anichini C, Di Bartolo RM, Bazzotti S, Morgese G, Balestri P. Grosso S, et al. Among authors: anichini c. Epilepsy Res. 2006 Dec;72(2-3):164-70. doi: 10.1016/j.eplepsyres.2006.07.016. Epub 2006 Sep 20. Epilepsy Res. 2006. PMID: 16987638

6

Electroencephalographic and epileptic patterns in X chromosome anomalies.

Grosso S, Farnetani MA, Di Bartolo RM, Berardi R, Pucci L, Mostardini R, Anichini C, Bartalini G, Galimberti D, Morgese G, Balestri P. Grosso S, et al. Among authors: anichini c. J Clin Neurophysiol. 2004 Jul-Aug;21(4):249-53. doi: 10.1097/00004691-200407000-00003. J Clin Neurophysiol. 2004. PMID: 15509914

7

Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12.

Grosso S, Pucci L, Farnetani M, Di Bartolo RM, Galimberti D, Mostardini R, Anichini C, Balestri M, Morgese G, Balestri P. Grosso S, et al. Among authors: anichini c. J Child Neurol. 2004 Aug;19(8):604-8. doi: 10.1177/088307380401900807. J Child Neurol. 2004. PMID: 15605470

8

Chromosome 18 aberrations and epilepsy: a review.

Grosso S, Pucci L, Di Bartolo RM, Gobbi G, Bartalini G, Anichini C, Scarinci R, Balestri M, Farnetani MA, Cioni M, Morgese G, Balestri P. Grosso S, et al. Among authors: anichini c. Am J Med Genet A. 2005 Apr 1;134A(1):88-94. doi: 10.1002/ajmg.a.30575. Am J Med Genet A. 2005. PMID: 15690352

9

Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.

Sparago A, Russo S, Cerrato F, Ferraiuolo S, Castorina P, Selicorni A, Schwienbacher C, Negrini M, Ferrero GB, Silengo MC, Anichini C, Larizza L, Riccio A. Sparago A, et al. Among authors: anichini c. Hum Mol Genet. 2007 Feb 1;16(3):254-64. doi: 10.1093/hmg/ddl448. Epub 2006 Dec 11. Hum Mol Genet. 2007. PMID: 17158821

10

Pubertal disorders in inv dup(15) syndrome.

Grosso S, Balestri P, Anichini C, Bartalini G, Pucci L, Morgese G, Berardi R. Grosso S, et al. Among authors: anichini c. Gynecol Endocrinol. 2001 Jun;15(3):165-9. Gynecol Endocrinol. 2001. PMID: 11447726

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

62 results

Search Page