Ritelli M - Search Results

1

Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic Stroke.

Bruno G, Ritelli M, Di Pietro A, Cipriano L, Colombi M, Lus G, Puoti G. Bruno G, et al. Among authors: ritelli m. J Stroke Cerebrovasc Dis. 2021 Jun;30(6):105744. doi: 10.1016/j.jstrokecerebrovasdis.2021.105744. Epub 2021 Apr 1. J Stroke Cerebrovasc Dis. 2021. PMID: 33813081

2

The FN13 peptide inhibits human tumor cells invasion through the modulation of alpha v beta 3 integrins organization and the inactivation of ILK pathway.

Zoppi N, Ritelli M, Salvi A, Colombi M, Barlati S. Zoppi N, et al. Among authors: ritelli m. Biochim Biophys Acta. 2007 Jun;1773(6):747-63. doi: 10.1016/j.bbamcr.2007.02.007. Epub 2007 Feb 24. Biochim Biophys Acta. 2007. PMID: 17383746 Free article.

3

Arterial tortuosity syndrome in two Italian paediatric patients.

Ritelli M, Drera B, Vicchio M, Puppini G, Biban P, Pilati M, Prioli MA, Barlati S, Colombi M. Ritelli M, et al. Orphanet J Rare Dis. 2009 Sep 25;4:20. doi: 10.1186/1750-1172-4-20. Orphanet J Rare Dis. 2009. PMID: 19781076 Free PMC article.

4

Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.

Drera B, Ritelli M, Zoppi N, Wischmeijer A, Gnoli M, Fattori R, Calzavara-Pinton PG, Barlati S, Colombi M. Drera B, et al. Among authors: ritelli m. Orphanet J Rare Dis. 2009 Nov 2;4:24. doi: 10.1186/1750-1172-4-24. Orphanet J Rare Dis. 2009. PMID: 19883511 Free PMC article.

5

Palmoplantar keratoderma, pseudo-ainhum, and universal atrichia: A new patient and review of the palmoplantar keratoderma-congenital alopecia syndrome.

Castori M, Valiante M, Ritelli M, Preziosi N, Colombi M, Paradisi M, Grammatico P. Castori M, et al. Among authors: ritelli m. Am J Med Genet A. 2010 Aug;152A(8):2043-7. doi: 10.1002/ajmg.a.33490. Am J Med Genet A. 2010. PMID: 20635335 Review.

6

Mutations in TGFBR2 gene cause spontaneous cervical artery dissection.

Pezzini A, Drera B, Del Zotto E, Ritelli M, Carletti M, Tomelleri G, Bovi P, Giossi A, Volonghi I, Costa P, Magoni M, Padovani A, Barlati S, Colombi M. Pezzini A, et al. Among authors: ritelli m. J Neurol Neurosurg Psychiatry. 2011 Dec;82(12):1372-4. doi: 10.1136/jnnp.2010.231902. Epub 2011 Jan 26. J Neurol Neurosurg Psychiatry. 2011. PMID: 21270064

7

Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio.

Chiarelli N, Ritelli M, Zoppi N, Benini A, Borsani G, Barlati S, Colombi M. Chiarelli N, et al. Among authors: ritelli m. Int J Dev Biol. 2011;55(2):229-36. doi: 10.1387/ijdb.103179nc. Int J Dev Biol. 2011. PMID: 21553381 Free article.

8

Clinical, neuroradiological and molecular features of a patient affected by pseudoxhantoma elasticum associated to carotid rete mirabile: case report.

Del Zotto E, Ritelli M, Pezzini A, Drera B, Gamba M, Giossi A, Volonghi I, Costa P, Barlati S, Gasparotti R, Padovani A, Colombi M. Del Zotto E, et al. Among authors: ritelli m. Clin Neurol Neurosurg. 2012 Jul;114(6):758-61. doi: 10.1016/j.clineuro.2011.12.031. Epub 2012 Jan 23. Clin Neurol Neurosurg. 2012. PMID: 22277295 No abstract available.

9

Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene.

Castori M, Ritelli M, Zoppi N, Molisso L, Chiarelli N, Zaccagna F, Grammatico P, Colombi M. Castori M, et al. Among authors: ritelli m. Am J Med Genet A. 2012 May;158A(5):1164-9. doi: 10.1002/ajmg.a.35266. Epub 2012 Apr 9. Am J Med Genet A. 2012. PMID: 22488877

10

Type III and V collagens modulate the expression and assembly of EDA(+) fibronectin in the extracellular matrix of defective Ehlers-Danlos syndrome fibroblasts.

Zoppi N, Ritelli M, Colombi M. Zoppi N, et al. Among authors: ritelli m. Biochim Biophys Acta. 2012 Oct;1820(10):1576-87. doi: 10.1016/j.bbagen.2012.06.004. Epub 2012 Jun 15. Biochim Biophys Acta. 2012. PMID: 22705941

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