A rare case of extradural thoracic spinal chordoma with medullary compression and literature review

Autor: Amalia Ene, Iulia Elena Petre, Aurelia Nicoleta Dabu

Publikováno v: Romanian Journal of Neurology, Vol 20, Iss 2, Pp 237-240 (2021)

Background. Chordomas are low-grade, slow-growing, but locally invasive and aggressive malignant tumors, arising from the remnants of the embryonic notochord. Given its origin, the distribution of chordomas is along the axial skeleton: 50% of cases i

Externí odkaz: https://doaj.org/article/b8dcacd3df67475abb8aee675db9074e

Clinical characteristics in patients with hereditary amyloidosis with Glu54Gln transthyretin identified in the Romanian population

Autor: Andreea Jercan, Amalia Ene, Ruxandra Jurcut, Mirela Draghici, Sorina Badelita, Mihaela Dragomir, Camelia Dobrea, Monica Popescu, Dumitru Jardan, Emanuel Stoica, Speranta Iacob, Ionela Codita, Claudiu Stan, Daniel Coriu

Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)

Abstract Background In Romania, 23 patients have been diagnosed with hereditary transthyretin amyloidosis (ATTRh), 18 of whom have the Glu54Gln mutation. This retrospective cohort included all patients with Glu54Gln-mutated ATTRh who were diagnosed i

Externí odkaz: https://doaj.org/article/c2b271c673c24582aaa937c8667f0036

Levodopa-carbidopa intestinal gel in advanced Parkinson's: Final results of the GLORIA registry

Autor: Amalia, Ene, Arnold, Guy, Bajenaru, Ovidiu, Bergmans, Bruno, Bjornara, Kari Anne, Blackie, Jeff, Bode, Matthias, Bourgeois, Paul, Bohlhalter, Stephan, Buraga, Ioan, Burkhard, Pierre R., Busson, Philippe, Calopa, Matilde, Clausen, Jesper, Danielsen, Erik Hvid, Defebvre, Luc, Delvaux, Valerie, Dethy, Sophie, Dietrichs, Espen, De Fabregues, Oriol, Gerhard, Ransmayr, Gusmaroli, Graziano, Hahn, Kirsten, Hauptmann, Björn, Henriksen, Tove, Hernandez-Vara, Jorge, Jeanjean, A., Kaiserova, Michaela, Kassubek, Jan, Kimber, Thomas, Konitsiotis, Spyridon, Krüger, Rejko, Kulisevsky, Jaime, Leenders, Jo, Lundqvist, Christofer, Ory Magne, F., Marano, Pietro, Milanov, Ivan, Modugno, Nicola, Misbahuddin, Anjum, Nevrly, Martin, Panayiotis, Zikos, Pedersen, Kenn Freddy, Pedersen, Stephen W., Perju-Dumbrava, Lacramioara, Ponsen, M.M., Popescu, Bogdan O., Rijntjes, Michel, Puente, V., Redecker, Christoph, Schrader, Christoph, Sensi, Mariachiara, Simu, Mihaela, Spanaki, Cleanthe, Storch, Alexander, Storstein, Anette, Tomantschger, Volker, van der Linden, Chris, van Laar, T., Viallet, F., Witjas, Tatiana, Wolz, Martin, Zibetti, Maurizio, Van Zandijcke, Michel, Antonini, Angelo, Poewe, Werner, Chaudhuri, K. Ray, Jech, Robert, Pickut, Barbara, Pirtošek, Zvezdan, Szasz, Jozsef, Valldeoriola, Francesc, Winkler, Christian, Bergmann, Lars, Yegin, Ashley, Onuk, Koray, Barch, David, Odin, Per

Publikováno v: In Parkinsonism and Related Disorders December 2017 45:13-20

A Parkinson's disease patient treated with deep brain stimulation, with implantation and reimplantation of the system - an 8 years follow-up

Autor: Gratiela Giurea-Neacsu, Amalia Ene, Bianca Nitu, Gabriel Iacob, Cornel Tudor, Paul Patrascu, Ovidiu Bajenaru, Bogdan O. Popescu

Publikováno v: Romanian Journal of Neurology, Vol 13, Iss 2, Pp 81-84 (2014)

Deep brain stimulation is the most used neurosurgical procedure for advanced Parkinson’s disease. This procedure improves motor symptoms and some non-motor symptoms over a long period of time. In rare cases there are several complications which mig

Externí odkaz: https://doaj.org/article/d1b3f59062e8481b85e47d4ed4ab033b

Clinical characteristics in patients with hereditary amyloidosis with Glu54Gln transthyretin identified in the Romanian population

Autor: Dumitru Jardan, Andreea Jercan, Emanuel Stoica, Sorina Badelita, Amalia Ene, Ionela Codita, Mihaela Dragomir, Speranta Iacob, Monica Popescu, Claudiu Stan, Camelia Dobrea, Daniel Coriu, Ruxandra Jurcut, Mirela Draghici

Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Orphanet Journal of Rare Diseases

Background In Romania, 23 patients have been diagnosed with hereditary transthyretin amyloidosis (ATTRh), 18 of whom have the Glu54Gln mutation. This retrospective cohort included all patients with Glu54Gln-mutated ATTRh who were diagnosed in Romania

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707ed9e27d945792af56c5e663eeb7da
https://doaj.org/article/c2b271c673c24582aaa937c8667f0036