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Tim D Cheetham

Showing results (21-30 of 27) with videos related to

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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 syndromeCatherine 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 StatusClaire L Wood, Robert Tinnion, Kieren G Hollingsworth, et al.
Hormone Research|March 5, 2009
Discordance for X-linked hypophosphataemic rickets in identical twin girlsCatherine 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 characteristicsLinda 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 DiseaseTim 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 UKFederica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Endocrine-Related Cancer|February 26, 2015
X-linked acrogigantism syndrome: clinical profile and therapeutic responsesAlbert Beckers, Maya Beth Lodish, Giampaolo Trivellin, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 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 syndromeCatherine 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 StatusClaire L Wood, Robert Tinnion, Kieren G Hollingsworth, et al.
Hormone Research|March 5, 2009
Discordance for X-linked hypophosphataemic rickets in identical twin girlsCatherine 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 characteristicsLinda 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 DiseaseTim 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 UKFederica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
Endocrine-Related Cancer|February 26, 2015
X-linked acrogigantism syndrome: clinical profile and therapeutic responsesAlbert Beckers, Maya Beth Lodish, Giampaolo Trivellin, et al.
Pageof 3