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Neurology
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June 2, 2010
Atypical idiopathic intracranial hypertension: normal BMI and older patients
B B Bruce, S Kedar, G P Van Stavern, et al.
The Journal of Rheumatology
|
June 1, 1995
Primary antiphospholipid syndrome is not associated with activated protein C resistance caused by factor V Arg 506 -->Gln mutation
V Biousse, J C Piette, C Frances, et al.
Neurology
|
October 27, 1997
De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy
V Biousse, M D Brown, N J Newman, et al.
Stroke
|
October 1, 1995
Internal carotid artery redundancy is significantly associated with dissection
I Ben Hamouda-M'Rad, V Biousse, M G Bousser, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 27, 2004
The use of contact lenses to treat visually symptomatic congenital nystagmus
V Biousse, R J Tusa, B Russell, et al.
BMJ (Clinical Research Ed.)
|
July 31, 1993
Migraine and risk of ischaemic stroke: a case-control study
C Tzourio, S Iglesias, J B Hubert, et al.
Neurology
|
January 27, 1998
Visual fields in patients with posterior GPi pallidotomy
V Biousse, N J Newman, C Carroll, et al.
AJNR. American Journal of Neuroradiology
|
November 14, 2007
Isolated progressive visual loss after coiling of paraclinoid aneurysms
G W Schmidt, S F Oster, K C Golnik, et al.
Revue Neurologique
|
January 1, 1994
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]
A Joutel, M G Bousser, V Biousse, et al.
Nature Genetics
|
September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19
A Joutel, M G Bousser, V Biousse, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 106) with videos related to
Sort By:
Page
of 11
Neurology
|
June 2, 2010
Atypical idiopathic intracranial hypertension: normal BMI and older patients
B B Bruce, S Kedar, G P Van Stavern, et al.
The Journal of Rheumatology
|
June 1, 1995
Primary antiphospholipid syndrome is not associated with activated protein C resistance caused by factor V Arg 506 -->Gln mutation
V Biousse, J C Piette, C Frances, et al.
Neurology
|
October 27, 1997
De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy
V Biousse, M D Brown, N J Newman, et al.
Stroke
|
October 1, 1995
Internal carotid artery redundancy is significantly associated with dissection
I Ben Hamouda-M'Rad, V Biousse, M G Bousser, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 27, 2004
The use of contact lenses to treat visually symptomatic congenital nystagmus
V Biousse, R J Tusa, B Russell, et al.
BMJ (Clinical Research Ed.)
|
July 31, 1993
Migraine and risk of ischaemic stroke: a case-control study
C Tzourio, S Iglesias, J B Hubert, et al.
Neurology
|
January 27, 1998
Visual fields in patients with posterior GPi pallidotomy
V Biousse, N J Newman, C Carroll, et al.
AJNR. American Journal of Neuroradiology
|
November 14, 2007
Isolated progressive visual loss after coiling of paraclinoid aneurysms
G W Schmidt, S F Oster, K C Golnik, et al.
Revue Neurologique
|
January 1, 1994
[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]
A Joutel, M G Bousser, V Biousse, et al.
Nature Genetics
|
September 1, 1993
A gene for familial hemiplegic migraine maps to chromosome 19
A Joutel, M G Bousser, V Biousse, et al.
Page
of 11