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Rinsho Hoshasen. Clinical Radiography
|
September 1, 1981
[A case of thanatophoric dysplasia with long survival (author's transl)]
S Hamada, T Miyamura, T Okimura, et al.
Pharmacogenetics and Genomics
|
September 27, 2006
A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance dose
Sarah K Tate, Rinki Singh, Chin-Chuan Hung, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 5, 2005
Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin
Sarah K Tate, Chantal Depondt, Sanjay M Sisodiya, et al.
Epilepsy Research
|
November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy
J M Lynch, S K Tate, P Kinirons, et al.
Oral Oncology
|
July 18, 2024
Development and clinical implementation of a digital workflow utilizing 3D-printed oral stents for patients with head and neck cancer receiving radiotherapy
Rance Tino, Millicent A Roach, Gabriela D Fuentes, et al.
Oral Oncology
|
February 19, 2025
Response to recent comments on "Development and clinical implementation of a digital workflow utilizing 3D-printed oral stents for patients with head and neck cancer receiving radiotherapy"
Rance B Tino, Millicent A Roach, Gabriela D Fuentes, et al.
The Lancet. Neurology
|
October 5, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
Gianpiero L Cavalleri, Michael E Weale, Kevin V Shianna, et al.
Brain : a Journal of Neurology
|
June 5, 2010
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
Dalia Kasperaviciūte, Claudia B Catarino, Erin L Heinzen, et al.
American Journal of Human Genetics
|
April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 59) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 59 results.
Rinsho Hoshasen. Clinical Radiography
|
September 1, 1981
[A case of thanatophoric dysplasia with long survival (author's transl)]
S Hamada, T Miyamura, T Okimura, et al.
Pharmacogenetics and Genomics
|
September 27, 2006
A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance dose
Sarah K Tate, Rinki Singh, Chin-Chuan Hung, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 5, 2005
Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin
Sarah K Tate, Chantal Depondt, Sanjay M Sisodiya, et al.
Epilepsy Research
|
November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy
J M Lynch, S K Tate, P Kinirons, et al.
Oral Oncology
|
July 18, 2024
Development and clinical implementation of a digital workflow utilizing 3D-printed oral stents for patients with head and neck cancer receiving radiotherapy
Rance Tino, Millicent A Roach, Gabriela D Fuentes, et al.
Oral Oncology
|
February 19, 2025
Response to recent comments on "Development and clinical implementation of a digital workflow utilizing 3D-printed oral stents for patients with head and neck cancer receiving radiotherapy"
Rance B Tino, Millicent A Roach, Gabriela D Fuentes, et al.
The Lancet. Neurology
|
October 5, 2007
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study
Gianpiero L Cavalleri, Michael E Weale, Kevin V Shianna, et al.
Brain : a Journal of Neurology
|
June 5, 2010
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study
Dalia Kasperaviciūte, Claudia B Catarino, Erin L Heinzen, et al.
American Journal of Human Genetics
|
April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Page
of 6