1. Study of rare familial monogenic dyslipidaemias in Portugal. (August 2018) Authors: Alves, A.C.; Graça, R.; Raimundo, A.; Sequeira, S.; Moldovan, O.; Lobarinhas, G.; Mansilha, H.; Duarte, S.; Gaspar, A.; Guerra, A.; Travessa, A.; Ferreira, A.; Bourbon, M. Journal: Atherosclerosis Issue: Volume 275(2018) Page Start: e226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Dunnigan-type familial partial lipodystrophy in a large Portuguese kindred. Issue 1 (July 2015) Authors: Alves, A.C.; Moldovan, O.; Medeiros, A.M.; Sousa, A.B.; Bourbon, M. Journal: Atherosclerosis Issue: Volume 241:Issue 1(2015) Page Start: e116 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Experimentally verified drain‐current model for variable barrier transistor. Issue 17 (5th August 2015) Authors: Moldovan, O.; Lime, F.; Barraud, S.; Smaani, B.; Latreche, S.; Iñiguez, B. Journal: Electronics letters Issue: Volume 51:Issue 17(2015) Page Start: 1364 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Familial chylomicronemia syndrome: Clinical and molecular characterization of individuals with clinical diagnosis in Portugal. (December 2020) Authors: Alves, A.C.; Abrantes, L.B.; Sequeira, S.; Moldovan, O.; Nunes, C.; Antunes, H.; Martins, E.; Gonçalves, R.; Duarte, J.S.; Gaspar, A.; Guerra, A.; Salgado, M.; Azevedo, A.C.; Figueiredo, M.; Palma, I.; Rato, Q.; Bourbon, M. Journal: Atherosclerosis Issue: Volume 315(2020) Page Start: e205 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Crystalline-like temperature dependence of the electrical characteristics in amorphous Indium-Gallium-Zinc-Oxide thin film transistors. (September 2017) Authors: Estrada, M.; Hernandez-Barrios, Y.; Cerdeira, A.; Ávila-Herrera, F.; Tinoco, J.; Moldovan, O.; Lime, F.; Iñiguez, B. Journal: Solid-state electronics Issue: Volume 135(2017) Page Start: 43 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 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) ↗