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Journal of Gastroenterology and Hepatology
|
July 30, 2021
Vedolizumab safety in pregnancy: Extricating drug from disease-related effects
R E Prentice, E K Wright, E Flanagan, et al.
Journal of the American Medical Informatics Association : JAMIA
|
April 20, 2013
The next-generation electronic health record: perspectives of key leaders from the US Department of Veterans Affairs
Jason J Saleem, Mindy E Flanagan, Nancy R Wilck, et al.
Ophthalmic Plastic and Reconstructive Surgery
|
March 21, 2009
High versus low concentration botulinum toxin A for benign essential blepharospasm: does dilution make a difference?
Michael H Boyle, Gerald McGwin, Courtney E Flanagan, et al.
Diabetes Research and Clinical Practice
|
October 14, 2014
Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: a life-changing diagnosis
Yotsapon Thewjitcharoen, Ekgaluck Wanothayaroj, Thep Himathongkam, et al.
Human Molecular Genetics
|
December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptoms
Roope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
May 10, 2018
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F <i>ABCC8</i> Mutation
Emregül Işık, Hüseyin Demirbilek, Jayne A. Houghton, et al.
Archives of Disease in Childhood
|
February 6, 2009
Hyperinsulinaemic hypoglycaemia
R R Kapoor, S E Flanagan, C James, et al.
Diabetologia
|
April 28, 2012
Functional MRI of the hypothalamic response to an oral glucose load
D E Flanagan, J Fulford, B Krishnan, et al.
The American Journal of Forensic Medicine and Pathology
|
July 17, 2024
Amniotic Fluid Embolism: An Illustrated Report and Review of Literature
Nicolas Kostelecky, Margarita Loxas, Rachel Multz, et al.
Diabetologia
|
April 13, 2006
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
S E Flanagan, E L Edghill, A L Gloyn, et al.
Page
of 59
Search research articles
Search
Showing results (151-160 of 582) with videos related to
Sort By:
Page
of 59
Journal of Gastroenterology and Hepatology
|
July 30, 2021
Vedolizumab safety in pregnancy: Extricating drug from disease-related effects
R E Prentice, E K Wright, E Flanagan, et al.
Journal of the American Medical Informatics Association : JAMIA
|
April 20, 2013
The next-generation electronic health record: perspectives of key leaders from the US Department of Veterans Affairs
Jason J Saleem, Mindy E Flanagan, Nancy R Wilck, et al.
Ophthalmic Plastic and Reconstructive Surgery
|
March 21, 2009
High versus low concentration botulinum toxin A for benign essential blepharospasm: does dilution make a difference?
Michael H Boyle, Gerald McGwin, Courtney E Flanagan, et al.
Diabetes Research and Clinical Practice
|
October 14, 2014
Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: a life-changing diagnosis
Yotsapon Thewjitcharoen, Ekgaluck Wanothayaroj, Thep Himathongkam, et al.
Human Molecular Genetics
|
December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptoms
Roope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
May 10, 2018
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F <i>ABCC8</i> Mutation
Emregül Işık, Hüseyin Demirbilek, Jayne A. Houghton, et al.
Archives of Disease in Childhood
|
February 6, 2009
Hyperinsulinaemic hypoglycaemia
R R Kapoor, S E Flanagan, C James, et al.
Diabetologia
|
April 28, 2012
Functional MRI of the hypothalamic response to an oral glucose load
D E Flanagan, J Fulford, B Krishnan, et al.
The American Journal of Forensic Medicine and Pathology
|
July 17, 2024
Amniotic Fluid Embolism: An Illustrated Report and Review of Literature
Nicolas Kostelecky, Margarita Loxas, Rachel Multz, et al.
Diabetologia
|
April 13, 2006
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype
S E Flanagan, E L Edghill, A L Gloyn, et al.
Page
of 59