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Diabetologia
|
April 28, 2016
Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk
Natascia Vedovato, Edward Cliff, Peter Proks, et al.
Cell Reports
|
January 12, 2017
Nutritional Programming of Lifespan by FOXO Inhibition on Sugar-Rich Diets
Adam J Dobson, Marina Ezcurra, Charlotte E Flanagan, et al.
Pediatric Diabetes
|
March 10, 2018
Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1
Huseyin Demirbilek, Nihal Hatipoglu, Ulku Gul, et al.
STAR Protocols
|
August 16, 2024
Protocol for hybrid structured-light three-dimensional scanning and modeling of human postmortem brains
Morgan Mekale Smith, Elizabeth Ochoa, Savannah Barannikov, et al.
Clinical Neuropathology
|
May 16, 2017
An unusual case of a young patient with Whipple's disease involving the central nervous system
Margaret E Flanagan, Nicole Andeen, Joshua Lieberman, et al.
Frontiers in Endocrinology
|
January 1, 2025
Congenital hyperinsulinism in the Ukraine: a 10-year national study
Evgenia Globa, Henrik Thybo Christesen, Michael Bau Mortensen, et al.
Diabetologia
|
October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODY
P Bowman, S E Flanagan, E L Edghill, et al.
Indian Journal of Pediatrics
|
May 24, 2019
Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1
Kakali Roy, Amit Kumar Satapathy, Jayne A L Houhton, et al.
ACS Combinatorial Science
|
July 9, 2019
On-DNA Decarboxylative Arylation: Merging Photoredox with Nickel Catalysis in Water
Dominik K Kölmel, Jiang Meng, Mei-Hsuan Tsai, et al.
Dermatology Online Journal
|
June 13, 2021
Subcutaneous metastasis from an atypical pulmonary carcinoid tumor
James T Pathoulas, Kelly E Flanagan, Chloe J Walker, et al.
Page
of 59
Search research articles
Search
Showing results (261-270 of 582) with videos related to
Sort By:
Page
of 59
Diabetologia
|
April 28, 2016
Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk
Natascia Vedovato, Edward Cliff, Peter Proks, et al.
Cell Reports
|
January 12, 2017
Nutritional Programming of Lifespan by FOXO Inhibition on Sugar-Rich Diets
Adam J Dobson, Marina Ezcurra, Charlotte E Flanagan, et al.
Pediatric Diabetes
|
March 10, 2018
Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1
Huseyin Demirbilek, Nihal Hatipoglu, Ulku Gul, et al.
STAR Protocols
|
August 16, 2024
Protocol for hybrid structured-light three-dimensional scanning and modeling of human postmortem brains
Morgan Mekale Smith, Elizabeth Ochoa, Savannah Barannikov, et al.
Clinical Neuropathology
|
May 16, 2017
An unusual case of a young patient with Whipple's disease involving the central nervous system
Margaret E Flanagan, Nicole Andeen, Joshua Lieberman, et al.
Frontiers in Endocrinology
|
January 1, 2025
Congenital hyperinsulinism in the Ukraine: a 10-year national study
Evgenia Globa, Henrik Thybo Christesen, Michael Bau Mortensen, et al.
Diabetologia
|
October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODY
P Bowman, S E Flanagan, E L Edghill, et al.
Indian Journal of Pediatrics
|
May 24, 2019
Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1
Kakali Roy, Amit Kumar Satapathy, Jayne A L Houhton, et al.
ACS Combinatorial Science
|
July 9, 2019
On-DNA Decarboxylative Arylation: Merging Photoredox with Nickel Catalysis in Water
Dominik K Kölmel, Jiang Meng, Mei-Hsuan Tsai, et al.
Dermatology Online Journal
|
June 13, 2021
Subcutaneous metastasis from an atypical pulmonary carcinoid tumor
James T Pathoulas, Kelly E Flanagan, Chloe J Walker, et al.
Page
of 59