Browsing eNauka
Browsing by Author Baets, J.
Showing results 1 to 7 of 7
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2013 | 4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder | Milic, Rasic V.; Nikodinovic, J.; Mladenovic, J.; De, Jonghe P.; Jordanova, A.; Baets, J.; Zimon, M.; Keckarević Marković, Milica | Article | 21M21 |
| 2013 | Clinical and neurophysiologic charactersitics of HINT1 neuropathy in Serbian patients | Milić-Rasić, M.; Nikodinović, J.; Mladenović, J.; Jordanova, A.; Baets, J.; Zimon, M.; De Jonghe, P.; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2015 | Elevated level of creatinine phosphokinase in the blood of patients with peripheral polyneuropathies | Mladenović, J.; Glumac, J. Nikodinović; Kosać, A.; Keckarević Marković, Milica | Conference Paper | 21M21 |
| 2015 | Is it easy to recognize HINT1 neuropathy (oral presentation) | Milić Rašić, V.; Branković, V.; Mladenović, J.; Nikodinović, J.; Kosac, A.; Baets, J.; De Jonghe, P.; Jordanova, A.; Zimon, M.; Keckarević-Marković, Milica | Conference Paper | Mp. category will be shown later |
| 2010 | Mutations in SACS cause atypical and late-onset forms of ARSACS | Baets, J.; Deconinck, T.; Smets, K.; Goossens, D.; Van, den Bergh P.; Dahan, K.; Schmedding, E.; Santens, P.; Rasic, V. M.; Van, Damme P.;
Robberecht, W.; De, Meirleir L.; Michielsens, B.; Del-Favero, J.; Jordanova, A.; De, Jonghe P.;
| Article | 21a+M21a+ |
| 2010 | N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome | Rakočević-Stojanović, V.; Milić Rašić, Vedrana | Article | 22M22 |
| 2015 | PP09.9 – 2907: Is it easy to recognize HINT1 neuropathy | Milić Rašić, Vedrana | Article | 21M21 |