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Journal of Neuroimmunology
|
June 1, 1995
In vivo clonal expression of T lymphocytes specific for an immunodominant N-terminal myelin basic protein epitope in healthy individuals
A Shanmugam, C Copie-Bergman, S Caillat, et al.
Neurology
|
April 1, 1991
MS and HTLV-I
O Gout, E Tournier-Lasserve, O Lyon-Caen, et al.
Archives of Neurology
|
February 15, 2001
Missense CACNA1A mutation causing episodic ataxia type 2
C Denier, A Ducros, A Durr, et al.
Stroke
|
November 1, 1994
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL
M M Ruchoux, H Chabriat, M G Bousser, et al.
Genes & Development
|
February 1, 1989
The Hox-1.3 homeo box protein is a sequence-specific DNA-binding phosphoprotein
W F Odenwald, J Garbern, H Arnheiter, et al.
Annals of Hematology
|
February 14, 2015
Acquired epidermodysplasia verruciformis, a new opportunistic infection related to bendamustine
P Cougoul, E Tournier, K Delavigne, et al.
Journal of Autoimmunity
|
October 10, 2001
A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French Caucasians
O Delrieu, D Dubois-Laforgue, J Timsit, et al.
Clinical and Experimental Dermatology
|
May 12, 2015
Late epidermal growth factor receptor inhibitor-related papulopustular rash: a distinct clinical entity
V Sibaud, E Tournier, H Roché, et al.
Cephalalgia : an International Journal of Headache
|
May 24, 2008
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation
A Lebas, L Guyant-Maréchal, D Hannequin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 18, 2009
Late onset hereditary episodic ataxia
M Damak, F Riant, M Boukobza, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 155) with videos related to
Sort By:
Page
of 16
Journal of Neuroimmunology
|
June 1, 1995
In vivo clonal expression of T lymphocytes specific for an immunodominant N-terminal myelin basic protein epitope in healthy individuals
A Shanmugam, C Copie-Bergman, S Caillat, et al.
Neurology
|
April 1, 1991
MS and HTLV-I
O Gout, E Tournier-Lasserve, O Lyon-Caen, et al.
Archives of Neurology
|
February 15, 2001
Missense CACNA1A mutation causing episodic ataxia type 2
C Denier, A Ducros, A Durr, et al.
Stroke
|
November 1, 1994
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL
M M Ruchoux, H Chabriat, M G Bousser, et al.
Genes & Development
|
February 1, 1989
The Hox-1.3 homeo box protein is a sequence-specific DNA-binding phosphoprotein
W F Odenwald, J Garbern, H Arnheiter, et al.
Annals of Hematology
|
February 14, 2015
Acquired epidermodysplasia verruciformis, a new opportunistic infection related to bendamustine
P Cougoul, E Tournier, K Delavigne, et al.
Journal of Autoimmunity
|
October 10, 2001
A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French Caucasians
O Delrieu, D Dubois-Laforgue, J Timsit, et al.
Clinical and Experimental Dermatology
|
May 12, 2015
Late epidermal growth factor receptor inhibitor-related papulopustular rash: a distinct clinical entity
V Sibaud, E Tournier, H Roché, et al.
Cephalalgia : an International Journal of Headache
|
May 24, 2008
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutation
A Lebas, L Guyant-Maréchal, D Hannequin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 18, 2009
Late onset hereditary episodic ataxia
M Damak, F Riant, M Boukobza, et al.
Page
of 16