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IEEE Transactions on Medical Imaging
|
July 9, 2019
Kinetic Modeling of Hyperpolarized Carbon-13 Pyruvate Metabolism in the Human Brain
Daniele Mammoli, Jeremy Gordon, Adam Autry, et al.
Journal of Medical Genetics
|
September 17, 2009
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
Bridget A Fernandez, Wendy Roberts, Brian Chung, et al.
Singapore Medical Journal
|
August 31, 2022
Clinical and neurocognitive outcomes after transcatheter aortic valve implantation (TAVI) with cerebral protection: initial experience with a novel dual-filter device in Southeast Asia
Paul Toon Lim Chiam, Nien Shen Chan, Yean Teng Lim, et al.
The Journal of Obstetrics and Gynaecology Research
|
September 12, 2017
Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong
Po Lam So, Kwun Yue Yvonne Cheng, Kwan Yiu Cheuk, et al.
BMJ Open
|
December 4, 2024
Effect of communicating genetic risk of type 2 diabetes and wearable technologies on wearable device-measured behavioural outcomes in East Asians: protocol of a randomised controlled trial
Youngwon Kim, Job G Godino, Flora Lai Tung Cheung, et al.
CJEM
|
July 22, 2016
An Environmental Scan of Academic Emergency Medicine at the 17 Canadian Medical Schools: Why Does this Matter to Emergency Physicians?
Ian G Stiell, Jennifer D Artz, Eddy S Lang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 9, 2015
Practical guidelines for managing adults with 22q11.2 deletion syndrome
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, et al.
Epilepsia
|
October 22, 2019
The epileptology of GNB5 encephalopathy
Gemma Poke, Chontelle King, Alison Muir, et al.
American Journal of Human Genetics
|
March 5, 2016
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis
James T Bennett, Tiong Yang Tan, Diana Alcantara, et al.
Human Mutation
|
February 16, 2022
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases
Nancy Vegas, Zeynep Demir, Christopher T Gordon, et al.
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Search research articles
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Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
IEEE Transactions on Medical Imaging
|
July 9, 2019
Kinetic Modeling of Hyperpolarized Carbon-13 Pyruvate Metabolism in the Human Brain
Daniele Mammoli, Jeremy Gordon, Adam Autry, et al.
Journal of Medical Genetics
|
September 17, 2009
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
Bridget A Fernandez, Wendy Roberts, Brian Chung, et al.
Singapore Medical Journal
|
August 31, 2022
Clinical and neurocognitive outcomes after transcatheter aortic valve implantation (TAVI) with cerebral protection: initial experience with a novel dual-filter device in Southeast Asia
Paul Toon Lim Chiam, Nien Shen Chan, Yean Teng Lim, et al.
The Journal of Obstetrics and Gynaecology Research
|
September 12, 2017
Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong
Po Lam So, Kwun Yue Yvonne Cheng, Kwan Yiu Cheuk, et al.
BMJ Open
|
December 4, 2024
Effect of communicating genetic risk of type 2 diabetes and wearable technologies on wearable device-measured behavioural outcomes in East Asians: protocol of a randomised controlled trial
Youngwon Kim, Job G Godino, Flora Lai Tung Cheung, et al.
CJEM
|
July 22, 2016
An Environmental Scan of Academic Emergency Medicine at the 17 Canadian Medical Schools: Why Does this Matter to Emergency Physicians?
Ian G Stiell, Jennifer D Artz, Eddy S Lang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 9, 2015
Practical guidelines for managing adults with 22q11.2 deletion syndrome
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, et al.
Epilepsia
|
October 22, 2019
The epileptology of GNB5 encephalopathy
Gemma Poke, Chontelle King, Alison Muir, et al.
American Journal of Human Genetics
|
March 5, 2016
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis
James T Bennett, Tiong Yang Tan, Diana Alcantara, et al.
Human Mutation
|
February 16, 2022
Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases
Nancy Vegas, Zeynep Demir, Christopher T Gordon, et al.
Page
of 6