Search research articles
Contact Us
Filters
Showing results (11-20 of 15) with videos related to
Page
of 2
Sort By:
You have reached the last page of results.
This site can display upto 15 results.
Epilepsy & Behavior : E&B
|
July 31, 2023
Gastrointestinal and eating problems in SCN1A-related seizure disorders
C A Minderhoud, A Postma, F E Jansen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 25, 2002
Endovascular coiling versus neurosurgical clipping in patients with a ruptured basilar tip aneurysm
E Lusseveld, E H Brilstra, P C G Nijssen, et al.
Brain : a Journal of Neurology
|
May 11, 2006
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
E Parrini, A Ramazzotti, W B Dobyns, et al.
Neurogenetics
|
July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new cases
I M de Lange, P Rump, R F Neuteboom, et al.
Neurogenetics
|
January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders
J J T van Harssel, S Weckhuysen, M J A van Kempen, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Epilepsy & Behavior : E&B
|
July 31, 2023
Gastrointestinal and eating problems in SCN1A-related seizure disorders
C A Minderhoud, A Postma, F E Jansen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 25, 2002
Endovascular coiling versus neurosurgical clipping in patients with a ruptured basilar tip aneurysm
E Lusseveld, E H Brilstra, P C G Nijssen, et al.
Brain : a Journal of Neurology
|
May 11, 2006
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
E Parrini, A Ramazzotti, W B Dobyns, et al.
Neurogenetics
|
July 3, 2017
Male patients affected by mosaic PCDH19 mutations: five new cases
I M de Lange, P Rump, R F Neuteboom, et al.
Neurogenetics
|
January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders
J J T van Harssel, S Weckhuysen, M J A van Kempen, et al.
Page
of 2