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Epilepsia
|
December 25, 2016
Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome
Atsushi Ishii, Joseph C Watkins, Debbie Chen, et al.
Molecular Biology and Evolution
|
August 17, 2018
The Role of Phylogenetically Conserved Elements in Shaping Patterns of Human Genomic Diversity
August E Woerner, Krishna R Veeramah, Joseph C Watkins, et al.
Journal of Molecular Evolution
|
January 1, 1987
Recruitment of lysozyme as a major enzyme in the mouse gut: duplication, divergence, and regulatory evolution
M F Hammer, J W Schilling, E M Prager, et al.
Epilepsia
|
November 18, 2024
Patients carrying pathogenic SCN8A variants with loss- and gain-of-function effects can be classified into five subgroups exhibiting varying developmental and epileptic components of encephalopathy
Joshua B Hack, Joseph C Watkins, John M Schreiber, et al.
The Journal of Clinical Investigation
|
October 1, 1989
Studies of osmotic diarrhea induced in normal subjects by ingestion of polyethylene glycol and lactulose
H F Hammer, C A Santa Ana, L R Schiller, et al.
Epilepsia
|
July 24, 2019
Influence of age at seizure onset on the acquisition of neurodevelopmental skills in an SCN8A cohort
Alejandra C Encinas, Ida Ki M Moore, Joseph C Watkins, et al.
Zeitschrift Fur Gastroenterologie
|
April 16, 2003
[Guidelines on diagnosis and therapy of the irritable bowel syndrome]
A Propst, H Vogelsang, F Renner, et al.
The American Journal of Cardiology
|
May 1, 1988
Changes in coronary blood flow and myocardial metabolism during aortic balloon valvuloplasty
M F Rousseau, W Wyns, F Hammer, et al.
Cleveland Clinic Journal of Medicine
|
November 1, 2023
Primary and secondary prevention of atherosclerotic cardiovascular disease: A case-based approach
Essa H Hariri, Mazen M Al Hammoud, Steven E Nissen, et al.
Genetics
|
June 7, 2005
Deep haplotype divergence and long-range linkage disequilibrium at xp21.1 provide evidence that humans descend from a structured ancestral population
Daniel Garrigan, Zahra Mobasher, Sarah B Kingan, et al.
Page
of 33
Search research articles
Search
Showing results (141-150 of 330) with videos related to
Sort By:
Page
of 33
Epilepsia
|
December 25, 2016
Clinical implications of SCN1A missense and truncation variants in a large Japanese cohort with Dravet syndrome
Atsushi Ishii, Joseph C Watkins, Debbie Chen, et al.
Molecular Biology and Evolution
|
August 17, 2018
The Role of Phylogenetically Conserved Elements in Shaping Patterns of Human Genomic Diversity
August E Woerner, Krishna R Veeramah, Joseph C Watkins, et al.
Journal of Molecular Evolution
|
January 1, 1987
Recruitment of lysozyme as a major enzyme in the mouse gut: duplication, divergence, and regulatory evolution
M F Hammer, J W Schilling, E M Prager, et al.
Epilepsia
|
November 18, 2024
Patients carrying pathogenic SCN8A variants with loss- and gain-of-function effects can be classified into five subgroups exhibiting varying developmental and epileptic components of encephalopathy
Joshua B Hack, Joseph C Watkins, John M Schreiber, et al.
The Journal of Clinical Investigation
|
October 1, 1989
Studies of osmotic diarrhea induced in normal subjects by ingestion of polyethylene glycol and lactulose
H F Hammer, C A Santa Ana, L R Schiller, et al.
Epilepsia
|
July 24, 2019
Influence of age at seizure onset on the acquisition of neurodevelopmental skills in an SCN8A cohort
Alejandra C Encinas, Ida Ki M Moore, Joseph C Watkins, et al.
Zeitschrift Fur Gastroenterologie
|
April 16, 2003
[Guidelines on diagnosis and therapy of the irritable bowel syndrome]
A Propst, H Vogelsang, F Renner, et al.
The American Journal of Cardiology
|
May 1, 1988
Changes in coronary blood flow and myocardial metabolism during aortic balloon valvuloplasty
M F Rousseau, W Wyns, F Hammer, et al.
Cleveland Clinic Journal of Medicine
|
November 1, 2023
Primary and secondary prevention of atherosclerotic cardiovascular disease: A case-based approach
Essa H Hariri, Mazen M Al Hammoud, Steven E Nissen, et al.
Genetics
|
June 7, 2005
Deep haplotype divergence and long-range linkage disequilibrium at xp21.1 provide evidence that humans descend from a structured ancestral population
Daniel Garrigan, Zahra Mobasher, Sarah B Kingan, et al.
Page
of 33