Search research articles
Contact Us
Filters
Showing results (141-150 of 278) with videos related to
Page
of 28
Sort By:
Pediatric Pulmonology
|
March 21, 2012
Interpretation of pediatric lung function: impact of ethnicity
J Kirkby, R Bonner, S Lum, et al.
Circulation. Cardiovascular Imaging
|
July 7, 2011
Diagnostic value of vena contracta area in the quantification of mitral regurgitation severity by color Doppler 3D echocardiography
Xin Zeng, Robert A Levine, Lanqi Hua, et al.
Molecular Psychiatry
|
May 25, 2007
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
T Lencz, T V Morgan, M Athanasiou, et al.
Journal of Clinical Medicine
|
October 29, 2020
Cell-Free DNA in the Investigation of Miscarriage
Emily Colley, Adam J Devall, Helen Williams, et al.
Platelets
|
March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function
Annabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.
Annals of Surgical Oncology
|
May 20, 2024
Impact of Neoadjuvant Chemoimmunotherapy on Surgical Outcomes and Time to Radiation in Triple-Negative Breast Cancer
Sara P Myers, Varadan Sevilimedu, V Morgan Jones, et al.
The Australian and New Zealand Journal of Psychiatry
|
May 2, 2000
Psychotic disorders in urban areas: an overview of the Study on Low Prevalence Disorders
A Jablensky, J McGrath, H Herrman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 2020
Asteroid impact, not volcanism, caused the end-Cretaceous dinosaur extinction
Alfio Alessandro Chiarenza, Alexander Farnsworth, Philip D Mannion, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 16, 2026
Performing Large-Scale Genetic Analysis in the Bleeding Disorders Community
Anna R Blankstein, Sterre P E Willems, Saskia E M Schols, et al.
The Turkish Journal of Pediatrics
|
June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene
Hakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.
Page
of 28
Search research articles
Search
Showing results (141-150 of 278) with videos related to
Sort By:
Page
of 28
Pediatric Pulmonology
|
March 21, 2012
Interpretation of pediatric lung function: impact of ethnicity
J Kirkby, R Bonner, S Lum, et al.
Circulation. Cardiovascular Imaging
|
July 7, 2011
Diagnostic value of vena contracta area in the quantification of mitral regurgitation severity by color Doppler 3D echocardiography
Xin Zeng, Robert A Levine, Lanqi Hua, et al.
Molecular Psychiatry
|
May 25, 2007
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
T Lencz, T V Morgan, M Athanasiou, et al.
Journal of Clinical Medicine
|
October 29, 2020
Cell-Free DNA in the Investigation of Miscarriage
Emily Colley, Adam J Devall, Helen Williams, et al.
Platelets
|
March 8, 2017
Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function
Annabel Maclachlan, Gerry Dolan, Charlotte Grimley, et al.
Annals of Surgical Oncology
|
May 20, 2024
Impact of Neoadjuvant Chemoimmunotherapy on Surgical Outcomes and Time to Radiation in Triple-Negative Breast Cancer
Sara P Myers, Varadan Sevilimedu, V Morgan Jones, et al.
The Australian and New Zealand Journal of Psychiatry
|
May 2, 2000
Psychotic disorders in urban areas: an overview of the Study on Low Prevalence Disorders
A Jablensky, J McGrath, H Herrman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 2020
Asteroid impact, not volcanism, caused the end-Cretaceous dinosaur extinction
Alfio Alessandro Chiarenza, Alexander Farnsworth, Philip D Mannion, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia
|
April 16, 2026
Performing Large-Scale Genetic Analysis in the Bleeding Disorders Community
Anna R Blankstein, Sterre P E Willems, Saskia E M Schols, et al.
The Turkish Journal of Pediatrics
|
June 2, 2009
Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene
Hakan Cangül, Ozlem Ozdemir, Tahsin Yakut, et al.
Page
of 28