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Nature
|
October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
A Joutel, C Corpechot, A Ducros, et al.
Neurology
|
June 17, 1999
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
C Denier, A Ducros, K Vahedi, et al.
American Journal of Human Genetics
|
January 1, 1996
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval
A Ducros, T Nagy, S Alamowitch, et al.
European Review for Medical and Pharmacological Sciences
|
May 18, 2021
Reversible cerebral vasoconstriction syndrome: a comprehensive systematic review
T-J Song, K H Lee, H Li, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 64) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 64 results.
Nature
|
October 24, 1996
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
A Joutel, C Corpechot, A Ducros, et al.
Neurology
|
June 17, 1999
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2
C Denier, A Ducros, K Vahedi, et al.
American Journal of Human Genetics
|
January 1, 1996
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval
A Ducros, T Nagy, S Alamowitch, et al.
European Review for Medical and Pharmacological Sciences
|
May 18, 2021
Reversible cerebral vasoconstriction syndrome: a comprehensive systematic review
T-J Song, K H Lee, H Li, et al.
Page
of 7