1. Antineoplastic agents exacerbating Charcot Marie Tooth disease: red flags to avoid permanent disability. (4th March 2018) Authors: Ibañez-Juliá, M. J.; Berzero, G.; Reyes-Botero, G.; Maisonobe, T.; Lenglet, T.; Slim, M.; Louis, S.; Balaguer, A.; Sanson, M.; Le Guern, E.; Latour, P.; Ricard, D.; Stojkovic, T.; Psimaras, D. Journal: Acta oncologica Issue: Volume 57:Number 3(2018) Page Start: 403 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Phenotypic spectrum of Charcot−Marie−Tooth disease due to LITAF/SIMPLE mutations: a study of 18 patients. (March 2017) Authors: Guimarães‐Costa, R.; Iancu Ferfoglia, R.; Leonard‐Louis, S.; Ziegler, F.; Magy, L.; Fournier, E.; Dubourg, O.; Bouche, P.; Maisonobe, T.; Lacour, A.; Moerman, A.; Latour, P.; Stojkovic, T. Journal: European journal of neurology Issue: Volume 24:Number 3(2017:Mar.) Page Start: 530 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Prediction of long‐term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke‐like episodes syndrome. (21st November 2016) Authors: Fayssoil, A.; Laforêt, P.; Bougouin, W.; Jardel, C.; Lombès, A.; Bécane, H. M.; Berber, N.; Stojkovic, T.; Béhin, A.; Eymard, B.; Duboc, D.; Wahbi, K. Journal: European journal of neurology Issue: Volume 24:Number 2(2017:Feb.) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T). (December 2016) Authors: Oestergaard, S.T.; Stojkovic, T.; Dahlqvist, J.R.; Bouchet-Seraphin, C.; Nectoux, J.; Leturcq, F.; Cossée, M.; Solé, G.; Thomsen, C.; Krag, T.O.; Vissing, J. Journal: Neurology Issue: Volume 2:Number 6(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families. (30th March 2018) Authors: Jonson, P. H.; Palmio, J.; Johari, M.; Penttilä, S.; Evilä, A.; Nelson, I.; Bonne, G.; Wiart, N.; Meyer, V.; Boland, A.; Deleuze, J.‐F.; Masson, C.; Stojkovic, T.; Chapon, F.; Romero, N. B.; Solé, G.; Ferrer, X.; Ferreiro, A.; Hackman, P.; Richard, I. Journal: European journal of neurology Issue: Volume 25:Number 5(2018) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. AB0510 Alphacalcidol Therapy Decreases GSH, SOD and Catalase Levels in Erythrocytes of Rheumatoid Arthritis Patients. (9th June 2015) Authors: Zivanovic Radnic, T.; Simic-Pasalic, K.; Sefik-Bukilica, M.; Misirlic Dencic, S.; Stojkovic, T.; Damjanov, N.; Vojinovic, J. Journal: Annals of the rheumatic diseases Issue: Volume 74(2015)Supplement 2 Page Start: 1069 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Clinical correlations and long‐term follow‐up in 100 patients with sarcoglycanopathies. (21st November 2020) Authors: Guimarães‐Costa, R.; Fernández‐Eulate, G.; Wahbi, K.; Leturcq, F.; Malfatti, E.; Behin, A.; Leonard‐Louis, S.; Desguerre, I.; Barnerias, C.; Nougues, M. C.; Isapof, A.; Estournet‐Mathiaud, B.; Quijano‐Roy, S.; Fayssoil, A.; Orlikowski, D.; Fauroux, B.; Richard, I.; Semplicini, C.; Romero, N. B.; ... Journal: European journal of neurology Issue: Volume 28:Number 2(2021) Page Start: 660 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Novel CAPN3 variant associated with an autosomal dominant calpainopathy. (10th June 2020) Authors: Cerino, M.; Campana‐Salort, E.; Salvi, A.; Cintas, P.; Renard, D.; Juntas Morales, R.; Tard, C.; Leturcq, F.; Stojkovic, T.; Bonello‐Palot, N.; Gorokhova, S.; Mortreux, J.; Maues De Paula, A.; Lévy, N.; Pouget, J.; Cossée, M.; Bartoli, M.; Krahn, M.; Attarian, S. Journal: Neuropathology & applied neurobiology Issue: Volume 46:Number 6(2020) Page Start: 564 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Demyelinating Charcot–Marie–Tooth neuropathy associated with FBLN5 mutations. (5th September 2020) Authors: Safka Brozkova, D.; Stojkovic, T.; Haberlová, J.; Mazanec, R.; Windhager, R.; Fernandes Rosenegger, P.; Hacker, S.; Züchner, S.; Kochański, A.; Leonard‐Louis, S.; Francou, B.; Latour, P.; Senderek, J.; Seeman, P.; Auer‐Grumbach, M. Journal: European journal of neurology Issue: Volume 27:Number 12(2020) Page Start: 2568 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Diagnostic power of the non‐ischaemic forearm exercise test in detecting glycogenosis type V. (5th March 2015) Authors: Hogrel, J.‐Y.; van den Bogaart, F.; Ledoux, I.; Ollivier, G.; Petit, F.; Koujah, N.; Béhin, A.; Stojkovic, T.; Eymard, B.; Voermans, N.; Laforêt, P. Journal: European journal of neurology Issue: Volume 22:Number 6(2015:Jun.) Page Start: 933 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗