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Journal of the Royal College of Physicians of London
|
January 23, 2019
A Note on Dr Frank Buckland
Alexander Cooke
Pediatric Neurology
|
October 19, 2024
Cenobamate's Efficacy for Seizure Treatment in Tuberous Sclerosis Complex
Gewalin Aungaroon, Alexander Cooke, David Ritter, et al.
ACS Applied Bio Materials
|
August 6, 2024
Targeted 8-arm PEG Nanosystems for Localization of Choroidal Neovascularization Macular Degeneration Model
Alan McLean, Wei Zhang, Alexander Cooke, et al.
Thrombosis Research
|
February 28, 2004
Relationship of the platelet glycoprotein PlA and fibrinogen T/G+1689 polymorphisms with peripheral arterial disease and ischaemic heart disease
Felicity B Smith, J Michael Connor, Amanda J Lee, et al.
European Journal of Gastroenterology & Hepatology
|
April 12, 2008
The biochemical and clinical penetrance of individuals diagnosed with genetic haemochromatosis by predictive genetic testing
Stuart Watkins, Douglas Thorburn, Neeraj Joshi, et al.
Cancer Research
|
October 19, 2018
The EGFR T790M Mutation Is Acquired through AICDA-Mediated Deamination of 5-Methylcytosine following TKI Treatment in Lung Cancer
Najwa El Kadi, Luo Wang, April Davis, et al.
European Journal of Medical Genetics
|
August 6, 2011
Clinical features and respiratory complications in Myhre syndrome
Ruth McGowan, Ramkumar Gulati, Pamela McHenry, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 23, 2011
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect
Phey M Yeap, Edward S Tobias, Eleni Mavraki, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Journal of the Royal College of Physicians of London
|
January 23, 2019
A Note on Dr Frank Buckland
Alexander Cooke
Pediatric Neurology
|
October 19, 2024
Cenobamate's Efficacy for Seizure Treatment in Tuberous Sclerosis Complex
Gewalin Aungaroon, Alexander Cooke, David Ritter, et al.
ACS Applied Bio Materials
|
August 6, 2024
Targeted 8-arm PEG Nanosystems for Localization of Choroidal Neovascularization Macular Degeneration Model
Alan McLean, Wei Zhang, Alexander Cooke, et al.
Thrombosis Research
|
February 28, 2004
Relationship of the platelet glycoprotein PlA and fibrinogen T/G+1689 polymorphisms with peripheral arterial disease and ischaemic heart disease
Felicity B Smith, J Michael Connor, Amanda J Lee, et al.
European Journal of Gastroenterology & Hepatology
|
April 12, 2008
The biochemical and clinical penetrance of individuals diagnosed with genetic haemochromatosis by predictive genetic testing
Stuart Watkins, Douglas Thorburn, Neeraj Joshi, et al.
Cancer Research
|
October 19, 2018
The EGFR T790M Mutation Is Acquired through AICDA-Mediated Deamination of 5-Methylcytosine following TKI Treatment in Lung Cancer
Najwa El Kadi, Luo Wang, April Davis, et al.
European Journal of Medical Genetics
|
August 6, 2011
Clinical features and respiratory complications in Myhre syndrome
Ruth McGowan, Ramkumar Gulati, Pamela McHenry, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 23, 2011
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect
Phey M Yeap, Edward S Tobias, Eleni Mavraki, et al.
Page
of 1