Tanya Stojkovic
Department of Neurology
Hôpital Roger Salengro
59037 Lille Cedex
France
Name/email consistency: high
- Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene. Stojkovic, T., Latour, P., Viet, G., de Seze, J., Hurtevent, J.F., Vandenberghe, A., Vermersch, P. Neuromuscul. Disord. (2004)
- Phrenic nerve palsy as a feature of chronic inflammatory demyelinating polyradiculoneuropathy. Stojkovic, T., De Seze, J., Hurtevent, J.F., Fourrier, F., Vermersch, P. Muscle. Nerve (2003)
- Congenital myopathy with central cores and fingerprint bodies in association with malignant hyperthermia susceptibility. Stojkovic, T., Maurage, C.A., Moerman, A., Hurtevent, J.F., Krivosic-Horber, R., Pellissier, J.F., Vermersch, P. Neuromuscul. Disord. (2001)
- Atypical form of non-Langerhans histiocytosis with disseminated brain and leptomeningeal lesions. Stojkovic, T., de Seze, J., Maurage, C.A., Rose, C., Hache, J.C., Vermersch, P. J. Neurol. Neurosurg. Psychiatr. (2000)
- Visual evoked potentials study in chronic idiopathic inflammatory demyelinating polyneuropathy. Stojkovic, T., de Seze, J., Hurtevent, J.F., Arndt, C., Beaume, A., Hache, J.C., Vermersch, P. Clin. Neurophysiol (2000)
- Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q). Stojkovic, T., Latour, P., Vandenberghe, A., Hurtevent, J.F., Vermersch, P. Neurology (1999)
