Stojkovic T - Search Results

1

NIPA1 (SPG6) mutations are a rare cause of autosomal dominant spastic paraplegia in Europe.

Klebe S, Lacour A, Durr A, Stojkovic T, Depienne C, Forlani S, Poea-Guyon S, Vuillaume I, Sablonniere B, Vermersch P, Brice A, Stevanin G. Klebe S, et al. Among authors: stojkovic t. Neurogenetics. 2007 Apr;8(2):155-7. doi: 10.1007/s10048-006-0074-9. Epub 2007 Jan 5. Neurogenetics. 2007. PMID: 17205300 No abstract available.

2

Mycophenolate mofetil and neurological diseases.

Vermersch P, Stojkovic T, de Seze J. Vermersch P, et al. Among authors: stojkovic t. Lupus. 2005;14 Suppl 1:s42-5. doi: 10.1191/0961203305lu2117oa. Lupus. 2005. PMID: 15803931 Review.

3

A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification.

Ferriby D, Stojkovic T, Sternberg D, Hurtevent JF, Hurtevent JP, Vermersch P. Ferriby D, et al. Among authors: stojkovic t. Neuromuscul Disord. 2006 May;16(5):321-4. doi: 10.1016/j.nmd.2006.01.015. Epub 2006 Apr 19. Neuromuscul Disord. 2006. PMID: 16624558

4

[Phenotypic aspects of FKRP-linked muscular dystrophy type 2I in a series of eleven patients].

Bourteel H, Stojkovic T, Cuisset JM, Maurage CA, Laforet P, Richard P, Vermersch P. Bourteel H, et al. Among authors: stojkovic t. Rev Neurol (Paris). 2007 Feb;163(2):189-96. doi: 10.1016/s0035-3787(07)90390-2. Rev Neurol (Paris). 2007. PMID: 17351538 French.

5

Periorbital ecchymoses are not pathognomonic of the light-chain type of amyloidosis.

Outteryck O, Stojkovic T, Launay D, Meignie-Ramon B, Vermersch P. Outteryck O, et al. Among authors: stojkovic t. Acta Derm Venereol. 2007;87(6):544-5. doi: 10.2340/00015555-0295. Acta Derm Venereol. 2007. PMID: 17989898 Free article. No abstract available.

6

[Paraplegia episodes revealing tuberculous myelitis].

Douay X, de Seze J, Stojkovic T, Gauvrit JY, Savage C, Pruvo JP, Vermersch P. Douay X, et al. Among authors: stojkovic t. Rev Neurol (Paris). 2000 Jul;156(6-7):661-4. Rev Neurol (Paris). 2000. PMID: 10891803 French.

7

[Interferons and neurologic diseases].

Vermersch P, de Seze J, Ferriby D, Stojkovic T. Vermersch P, et al. Among authors: stojkovic t. Rev Med Interne. 2002 Nov;23 Suppl 4:475s-480s. doi: 10.1016/s0248-8663(02)00661-6. Rev Med Interne. 2002. PMID: 12481402 Review. French.

8

Relapsing demyelinating disease affecting both the central and peripheral nervous systems.

Zéphir H, Stojkovic T, Latour P, Lacour A, de Seze J, Outteryck O, Maurage CA, Monpeurt C, Chatelet P, Ovelacq E, Vermersch P. Zéphir H, et al. Among authors: stojkovic t. J Neurol Neurosurg Psychiatry. 2008 Sep;79(9):1032-9. doi: 10.1136/jnnp.2006.108290. Epub 2008 Jan 21. J Neurol Neurosurg Psychiatry. 2008. PMID: 18208860

9

Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome.

Outteryck O, Richard P, Lacour A, Fournier E, Zéphir H, Gaudon K, Eymard B, Hantaï D, Vermersch P, Stojkovic T. Outteryck O, et al. Among authors: stojkovic t. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):450-1. doi: 10.1136/jnnp.2008.148189. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289485 No abstract available.

10

Early dopasensitive Parkinsonism related to myotonic dystrophy type 2.

Annic A, Devos D, Destée A, Defebvre L, Lacour A, Hurtevent JF, Stojkovic T. Annic A, et al. Among authors: stojkovic t. Mov Disord. 2008 Oct 30;23(14):2100-1. doi: 10.1002/mds.22239. Mov Disord. 2008. PMID: 18759330 No abstract available.

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