1. Montelukast and cardiovascular risk in asthmatics. (August 2021) Authors: Hoxha, M.; Malaj, V.; Tedesco, C.C.; Quaglini, S.; Capra, V.; Sala, A.; Rovati, G.E. Journal: Atherosclerosis Issue: Volume 331(2021) Page Start: e271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2. (April 2016) Authors: Fiorillo, C.; Moro, F.; Brisca, G.; Accogli, A.; Trucco, F.; Trovato, R.; Pedemonte, M.; Severino, M.; Catala, M.; Capra, V.; Santorelli, F. M.; Bruno, C.; Rossi, A.; Minetti, C. Journal: European journal of neurology Issue: Volume 23:Number 4(2016:Apr.) Page Start: e19 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations. (September 2020) Authors: Villa, R.; Fergnani, V.G.C.; Silipigni, R.; Guerneri, S.; Cinnante, C.; Guala, A.; Danesino, C.; Scola, E.; Conte, G.; Fumagalli, M.; Gangi, S.; Colombo, L.; Picciolini, O.; Ajmone, P.F.; Accogli, A.; Madia, F.; Tassano, E.; Scala, M.; Capra, V.; Srour, M. Journal: European journal of paediatric neurology Issue: Volume 28(2020) Page Start: 110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. In vitro pharmacological evaluation of multitarget thromboxane prostanoid receptor/COX-2 agents: A possible strategy to solve the cardiovascular issues of COXIBs. (September 2016) Authors: Hoxha, M.; Buccellati, C.; Capra, V.; Cena, C.; Sala, A.; Bertinaria, M.; Rovati, G. Journal: Atherosclerosis Issue: Volume 252(2016) Page Start: e59 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Impact of vascular thromboxane prostanoid receptor activation on hemostasis, thrombosis, oxidative stress, and inflammation. (February 2014) Authors: Capra, V.; Bäck, M.; Angiolillo, D. J.; Cattaneo, M.; Sakariassen, K. S. Journal: Journal of thrombosis and haemostasis Issue: Volume 12:Number 2(2014:Feb.) Page Start: 126 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1. Issue 2 (5th December 2013) Authors: Capra, V.; Severino, M.; Rossi, A.; Nozza, P.; Doneda, C.; Perri, K.; Pavanello, M.; Fiorio, P.; Gimelli, G.; Tassano, E.; Di Battista, E. Journal: American journal of medical genetics Issue: Volume 164:Issue 2(2014.) Page Start: 495 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The DRY motif at work: the P2Y12 receptor case. (May 2014) Authors: Rovati, G. E.; Capra, V. Journal: Journal of thrombosis and haemostasis Issue: Volume 12:Number 5(2014:May) Page Start: 713 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations. Issue 1 (10th September 2014) Authors: Merello, E.; Mascelli, S.; Raso, A.; Piatelli, G.; Consales, A.; Cama, A.; Kibar, Z.; Capra, V.; Marco, Patrizia De Journal: Birth defects research Issue: Volume 103:Issue 1(2015) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund–Thomson/Baller‐Gerold syndromes. (26th March 2014) Authors: Piard, J.; Aral, B.; Vabres, P.; Holder‐Espinasse, M.; Mégarbané, A.; Gauthier, S.; Capra, V.; Pierquin, G.; Callier, P.; Baumann, C.; Pasquier, L.; Baujat, G.; Martorell, L.; Rodriguez, A.; Brady, A. F.; Boralevi, F.; González‐Enseñat, M. A.; Rio, M.; Bodemer, C.; Philip, N. Journal: Clinical genetics Issue: Volume 87:Number 3(2015:Mar.) Page Start: 244 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗