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Journal of Neurology
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July 5, 2001
Guillain-Barré syndrome resembling brainstem death in a patient with brain injury
T Stojkovic, M Verdin, J F Hurtevent, et al.
Journal of Neurology
|
October 31, 2003
Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosis
C Monaca-Charley, T Stojkovic, A Duhamel, et al.
Neuromuscular Disorders : NMD
|
April 21, 2006
A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification
D Ferriby, T Stojkovic, D Sternberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 1997
Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile form
T Stojkovic, L Defebvre, X Quilliet, et al.
Revue Neurologique
|
December 17, 2004
[Guillain-Barré syndrome with hallucinations and onirism: an underestimated association]
E Le Rhun, J de Sèze, T Stojkovic, et al.
Revue Neurologique
|
July 5, 2001
[Sarcoidosis and progressive multifocal leukoencephalopathy]
M A Mackowiak-Cordoliani, J De Seze, T Stojkovic, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 14, 2000
Atypical form of non-Langerhans histiocytosis with disseminated brain and leptomeningeal lesions
T Stojkovic, J de Seze, C A Maurage, et al.
Neuromuscular Disorders : NMD
|
June 26, 2024
Rapidly progressive myopathy: unveiling light chain amyloidosis as an initial manifestation of multiple myeloma: a case report and literature review
P Kaminskiene, T Stojkovic, D Roos-Weil, et al.
Revue Neurologique
|
December 21, 2005
[Tonic pupils in Sjögren's syndrome]
P Vermersch, S Dufourd-Delalande, S Defoort-Dhellemmes, et al.
Mutation Research
|
December 2, 1996
Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene
X Quilliet, O Chevallier-Lagente, E Eveno, et al.
Page
of 13
Search research articles
Search
Showing results (31-40 of 121) with videos related to
Sort By:
Page
of 13
Journal of Neurology
|
July 5, 2001
Guillain-Barré syndrome resembling brainstem death in a patient with brain injury
T Stojkovic, M Verdin, J F Hurtevent, et al.
Journal of Neurology
|
October 31, 2003
Double-blind crossover study with dolasetron mesilate, a 5-HT3 receptor antagonist in cerebellar syndrome secondary to multiple sclerosis
C Monaca-Charley, T Stojkovic, A Duhamel, et al.
Neuromuscular Disorders : NMD
|
April 21, 2006
A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification
D Ferriby, T Stojkovic, D Sternberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 1, 1997
Neurological manifestations in two related xeroderma pigmentosum group D patients: complications of the late-onset type of the juvenile form
T Stojkovic, L Defebvre, X Quilliet, et al.
Revue Neurologique
|
December 17, 2004
[Guillain-Barré syndrome with hallucinations and onirism: an underestimated association]
E Le Rhun, J de Sèze, T Stojkovic, et al.
Revue Neurologique
|
July 5, 2001
[Sarcoidosis and progressive multifocal leukoencephalopathy]
M A Mackowiak-Cordoliani, J De Seze, T Stojkovic, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 14, 2000
Atypical form of non-Langerhans histiocytosis with disseminated brain and leptomeningeal lesions
T Stojkovic, J de Seze, C A Maurage, et al.
Neuromuscular Disorders : NMD
|
June 26, 2024
Rapidly progressive myopathy: unveiling light chain amyloidosis as an initial manifestation of multiple myeloma: a case report and literature review
P Kaminskiene, T Stojkovic, D Roos-Weil, et al.
Revue Neurologique
|
December 21, 2005
[Tonic pupils in Sjögren's syndrome]
P Vermersch, S Dufourd-Delalande, S Defoort-Dhellemmes, et al.
Mutation Research
|
December 2, 1996
Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene
X Quilliet, O Chevallier-Lagente, E Eveno, et al.
Page
of 13