Search research articles
Contact Us
Filters
Showing results (21-30 of 27) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 27 results.
The Journal of Clinical Endocrinology and Metabolism
|
December 13, 2003
Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome
Catherine J Owen, Claire E Jennings, Helen Imrie, et al.
Nutrients
|
December 11, 2022
Muscle Function, Body Composition, Insulin Sensitivity and Physical Activity in Adolescents Born Preterm: Impact of Gestation and Vitamin D Status
Claire L Wood, Robert Tinnion, Kieren G Hollingsworth, et al.
Hormone Research
|
March 5, 2009
Discordance for X-linked hypophosphataemic rickets in identical twin girls
Catherine J Owen, Abdul Habeb, Simon H S Pearce, et al.
Human Reproduction (Oxford, England)
|
February 7, 2003
A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics
Linda A Allen, John C Achermann, Pirjo Pakarinen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 23, 2021
Adjuvant Rituximab-Exploratory Trial in Young People With Graves Disease
Tim D Cheetham, Michael Cole, Mario Abinun, et al.
Journal of the Endocrine Society
|
July 14, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK
Federica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Endocrine-Related Cancer
|
February 26, 2015
X-linked acrogigantism syndrome: clinical profile and therapeutic responses
Albert Beckers, Maya Beth Lodish, Giampaolo Trivellin, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
The Journal of Clinical Endocrinology and Metabolism
|
December 13, 2003
Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome
Catherine J Owen, Claire E Jennings, Helen Imrie, et al.
Nutrients
|
December 11, 2022
Muscle Function, Body Composition, Insulin Sensitivity and Physical Activity in Adolescents Born Preterm: Impact of Gestation and Vitamin D Status
Claire L Wood, Robert Tinnion, Kieren G Hollingsworth, et al.
Hormone Research
|
March 5, 2009
Discordance for X-linked hypophosphataemic rickets in identical twin girls
Catherine J Owen, Abdul Habeb, Simon H S Pearce, et al.
Human Reproduction (Oxford, England)
|
February 7, 2003
A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics
Linda A Allen, John C Achermann, Pirjo Pakarinen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 23, 2021
Adjuvant Rituximab-Exploratory Trial in Young People With Graves Disease
Tim D Cheetham, Michael Cole, Mario Abinun, et al.
Journal of the Endocrine Society
|
July 14, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK
Federica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Endocrine-Related Cancer
|
February 26, 2015
X-linked acrogigantism syndrome: clinical profile and therapeutic responses
Albert Beckers, Maya Beth Lodish, Giampaolo Trivellin, et al.
Page
of 3