Search research articles
Contact Us
Filters
Showing results (21-30 of 123) with videos related to
Page
of 13
Sort By:
European Journal of Human Genetics : EJHG
|
June 3, 1999
Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families
S Laberge, P Labauge, E Maréchal, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1996
Prevalence of serum antibodies to hepatitis C virus is not increased in patients with multiple sclerosis
O Heinzlef, E Roullet, C Johanet, et al.
Lancet (London, England)
|
December 24, 1998
Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie
P Labauge, S Laberge, L Brunereau, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 30, 2009
Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood
P Bertholon, S Chabrier, F Riant, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 21, 2009
Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations
J Sirvente, O Enjolras, M Wassef, et al.
Journal of Neurology
|
March 16, 2012
Presymptomatic genetic testing in CADASIL
S Reyes, A Kurtz, D Hervé, et al.
La Revue De Medecine Interne
|
November 25, 1998
[Immunogenetic bases of systemic lupus erythematosus in humans]
M Michel, O Meyer, C Françès, et al.
American Journal of Medical Genetics
|
November 11, 1996
An additional monogenic disorder that masquerades as multiple sclerosis
K Vahedi, E Tournier-Lasserve, K Vahedi, et al.
Stroke
|
January 1, 1993
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study
M Baudrimont, F Dubas, A Joutel, et al.
Stroke
|
October 1, 1991
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy
E Tournier-Lasserve, M T Iba-Zizen, N Romero, et al.
Page
of 13
Search research articles
Search
Showing results (21-30 of 123) with videos related to
Sort By:
Page
of 13
European Journal of Human Genetics : EJHG
|
June 3, 1999
Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families
S Laberge, P Labauge, E Maréchal, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1996
Prevalence of serum antibodies to hepatitis C virus is not increased in patients with multiple sclerosis
O Heinzlef, E Roullet, C Johanet, et al.
Lancet (London, England)
|
December 24, 1998
Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie
P Labauge, S Laberge, L Brunereau, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 30, 2009
Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood
P Bertholon, S Chabrier, F Riant, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 21, 2009
Frequency and phenotypes of cutaneous vascular malformations in a consecutive series of 417 patients with familial cerebral cavernous malformations
J Sirvente, O Enjolras, M Wassef, et al.
Journal of Neurology
|
March 16, 2012
Presymptomatic genetic testing in CADASIL
S Reyes, A Kurtz, D Hervé, et al.
La Revue De Medecine Interne
|
November 25, 1998
[Immunogenetic bases of systemic lupus erythematosus in humans]
M Michel, O Meyer, C Françès, et al.
American Journal of Medical Genetics
|
November 11, 1996
An additional monogenic disorder that masquerades as multiple sclerosis
K Vahedi, E Tournier-Lasserve, K Vahedi, et al.
Stroke
|
January 1, 1993
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study
M Baudrimont, F Dubas, A Joutel, et al.
Stroke
|
October 1, 1991
Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy
E Tournier-Lasserve, M T Iba-Zizen, N Romero, et al.
Page
of 13