Casali B - Search Results

1

Very early onset and severe complicated phenotype caused by a new spastic paraplegia 3A gene mutation.

Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Della Giustina E. Fusco C, et al. Among authors: casali b. J Child Neurol. 2012 Oct;27(10):1348-50. doi: 10.1177/0883073811435245. Epub 2012 Feb 28. J Child Neurol. 2012. PMID: 22378671

2

Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation.

Fusco C, Frattini D, Farnetti E, Nicoli D, Casali B, Fiorentino F, Nuccitelli A, Giustina ED. Fusco C, et al. Among authors: casali b. Brain Dev. 2010 Aug;32(7):592-4. doi: 10.1016/j.braindev.2009.08.003. Epub 2009 Sep 6. Brain Dev. 2010. PMID: 19735987

3

A clinical phenotype mimicking essential hypertension in a newly discovered family with Liddle's syndrome.

Rossi E, Farnetti E, Nicoli D, Sazzini M, Perazzoli F, Regolisti G, Grasselli C, Santi R, Negro A, Mazzeo V, Mantero F, Luiselli D, Casali B. Rossi E, et al. Among authors: casali b. Am J Hypertens. 2011 Aug;24(8):930-5. doi: 10.1038/ajh.2011.76. Epub 2011 Apr 28. Am J Hypertens. 2011. PMID: 21525970

4

Liddle's syndrome caused by a novel missense mutation (P617L) of the epithelial sodium channel beta subunit.

Rossi E, Farnetti E, Debonneville A, Nicoli D, Grasselli C, Regolisti G, Negro A, Perazzoli F, Casali B, Mantero F, Staub O. Rossi E, et al. Among authors: casali b. J Hypertens. 2008 May;26(5):921-7. doi: 10.1097/HJH.0b013e3282f85dfe. J Hypertens. 2008. PMID: 18398334

5

Haptoglobin phenotype and epithelial ovarian cancer.

Mandato VD, Magnani E, Abrate M, Casali B, Nicoli D, Farnetti E, Formisano D, Pirillo D, Ciarlini G, De Iaco P, Strada I, Zamagni C, La Sala GB. Mandato VD, et al. Among authors: casali b. Anticancer Res. 2012 Oct;32(10):4353-8. Anticancer Res. 2012. PMID: 23060558

6

Vascular endothelial growth factor gene polymorphisms in giant cell arteritis.

Boiardi L, Casali B, Nicoli D, Farnetti E, Chen Q, Macchioni P, Catanoso MG, Pulsatelli L, Meliconi R, Salvarani C. Boiardi L, et al. Among authors: casali b. J Rheumatol. 2003 Oct;30(10):2160-4. J Rheumatol. 2003. PMID: 14528511

7

Endothelial nitric oxide synthase gene polymorphisms in giant cell arteritis.

Salvarani C, Casali B, Nicoli D, Farnetti E, Macchioni P, Catanoso MG, Chen Q, Bajocchi G, Boiardi L. Salvarani C, et al. Among authors: casali b. Arthritis Rheum. 2003 Nov;48(11):3219-23. doi: 10.1002/art.11307. Arthritis Rheum. 2003. PMID: 14613286 Free article.

8

Interleukin-6 promoter polymorphism at position -174 in giant cell arteritis.

Salvarani C, Casali B, Farnetti E, Pipitone N, Nicoli D, Macchioni P, Cimino L, Bajocchi G, Catanoso MG, Boiardi L. Salvarani C, et al. Among authors: casali b. J Rheumatol. 2005 Nov;32(11):2173-7. J Rheumatol. 2005. PMID: 16265697

9

Interleukin-10 promoter polymorphisms in giant cell arteritis.

Boiardi L, Casali B, Farnetti E, Pipitone N, Nicoli D, Macchioni P, Cimino L, Bajocchi G, Catanoso MG, Pattacini L, Salvarani C. Boiardi L, et al. Among authors: casali b. Arthritis Rheum. 2006 Dec;54(12):4011-7. doi: 10.1002/art.22218. Arthritis Rheum. 2006. PMID: 17133531 Free article.

10

CC chemokine receptor 5 polymorphism in chronic periaortitis.

Boiardi L, Vaglio A, Nicoli D, Farnetti E, Palmisano A, Pipitone N, Maritati F, Casali B, Martorana D, Moroni G, Gallelli B, Buzio C, Salvarani C. Boiardi L, et al. Among authors: casali b. Rheumatology (Oxford). 2011 Jun;50(6):1025-32. doi: 10.1093/rheumatology/keq416. Epub 2011 Jan 21. Rheumatology (Oxford). 2011. PMID: 21258050

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