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Hormone Research in Paediatrics
|
May 26, 2023
Evaluating Eating Behaviour, Energy Homeostasis, and Obesity in Childhood-Onset Craniopharyngioma: A Feasibility Study
Elanor C Hinton, Fiona E Lithander, Rebecca L Elsworth, et al.
Human Brain Mapping
|
May 5, 2023
Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging
Alice E Thackray, Elanor C Hinton, Turki M Alanazi, et al.
Journal of Medical Genetics
|
November 29, 2013
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype
Alexander J Hamilton, Coralie Bingham, Timothy J McDonald, et al.
Nature Communications
|
September 2, 2015
Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans
Louise E Docherty, Faisal I Rezwan, Rebecca L Poole, et al.
Journal of Medical Genetics
|
March 26, 2018
Maternal variants in <i>NLRP</i> and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring
Matthias Begemann, Faisal I Rezwan, Jasmin Beygo, et al.
Journal of the American Society of Nephrology : JASN
|
April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2
Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.
Page
of 4
Search research articles
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Showing results (31-40 of 36) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 36 results.
Hormone Research in Paediatrics
|
May 26, 2023
Evaluating Eating Behaviour, Energy Homeostasis, and Obesity in Childhood-Onset Craniopharyngioma: A Feasibility Study
Elanor C Hinton, Fiona E Lithander, Rebecca L Elsworth, et al.
Human Brain Mapping
|
May 5, 2023
Exploring the acute effects of running on cerebral blood flow and food cue reactivity in healthy young men using functional magnetic resonance imaging
Alice E Thackray, Elanor C Hinton, Turki M Alanazi, et al.
Journal of Medical Genetics
|
November 29, 2013
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype
Alexander J Hamilton, Coralie Bingham, Timothy J McDonald, et al.
Nature Communications
|
September 2, 2015
Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans
Louise E Docherty, Faisal I Rezwan, Rebecca L Poole, et al.
Journal of Medical Genetics
|
March 26, 2018
Maternal variants in <i>NLRP</i> and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring
Matthias Begemann, Faisal I Rezwan, Jasmin Beygo, et al.
Journal of the American Society of Nephrology : JASN
|
April 5, 2017
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2
Oscar Rubio Cabezas, Sarah E Flanagan, Horia Stanescu, et al.
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of 4