Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J W Gregory

Showing results (41-50 of 79) with videos related to

Pageof 8
Sort By:
Archives of Disease in Childhood|May 1, 1989
Dietary treatment of hyperlysinaemiaJ W Gregory, N Beail, N A Boyle, et al.
Pediatric Research|August 6, 2000
Proliferative response of different human osteoblast-like cell models to proinflammatory cytokinesM E Harbour, J W Gregory, H R Jenkins, et al.
Archives of Disease in Childhood|February 1, 1991
Body water measurement in growth disorders: a comparison of bioelectrical impedance and skinfold thickness techniques with isotope dilutionJ W Gregory, S A Greene, C M Scrimgeour, et al.
Archives of Disease in Childhood|January 8, 2004
Pitfalls in the assessment of body composition in survivors of acute lymphoblastic leukaemiaJ T Warner, W D Evans, D K H Webb, et al.
Archives of Disease in Childhood|May 27, 2003
Hypoparathyroidism and 22q11 deletion syndromeS C Taylor, G Morris, D Wilson, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|March 23, 2011
The experiences of children and their parents in paediatric diabetes services should inform the development of communication skills for healthcare staff (the DEPICTED Study)K Hawthorne, K Bennert, L Lowes, et al.
Diabetes Research and Clinical Practice|March 12, 2021
The changing incidence of childhood-onset type 1 diabetes in Wales: Effect of gender and season at diagnosis and birthJ N Harvey, R Hibbs, M J Maguire, et al.
Human Genetics|February 14, 2007
Gene symbol: AVP. Disease: Diabetes insipidus, neurohypophyseal. Accession #Hm0560A P Abbes, J H Davies, M Penney, et al.
Hormone Research|October 29, 2005
Clinical features, diagnosis and molecular studies of familial central diabetes insipidusJ H Davies, M Penney, A P Abbes, et al.
The Journal of Clinical Endocrinology and Metabolism|March 12, 2003
The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian populationN Jordan, N Williams, J W Gregory, et al.
Pageof 8

Showing results (41-50 of 79) with videos related to

Sort By:
Pageof 8
Archives of Disease in Childhood|May 1, 1989
Dietary treatment of hyperlysinaemiaJ W Gregory, N Beail, N A Boyle, et al.
Pediatric Research|August 6, 2000
Proliferative response of different human osteoblast-like cell models to proinflammatory cytokinesM E Harbour, J W Gregory, H R Jenkins, et al.
Archives of Disease in Childhood|February 1, 1991
Body water measurement in growth disorders: a comparison of bioelectrical impedance and skinfold thickness techniques with isotope dilutionJ W Gregory, S A Greene, C M Scrimgeour, et al.
Archives of Disease in Childhood|January 8, 2004
Pitfalls in the assessment of body composition in survivors of acute lymphoblastic leukaemiaJ T Warner, W D Evans, D K H Webb, et al.
Archives of Disease in Childhood|May 27, 2003
Hypoparathyroidism and 22q11 deletion syndromeS C Taylor, G Morris, D Wilson, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|March 23, 2011
The experiences of children and their parents in paediatric diabetes services should inform the development of communication skills for healthcare staff (the DEPICTED Study)K Hawthorne, K Bennert, L Lowes, et al.
Diabetes Research and Clinical Practice|March 12, 2021
The changing incidence of childhood-onset type 1 diabetes in Wales: Effect of gender and season at diagnosis and birthJ N Harvey, R Hibbs, M J Maguire, et al.
Human Genetics|February 14, 2007
Gene symbol: AVP. Disease: Diabetes insipidus, neurohypophyseal. Accession #Hm0560A P Abbes, J H Davies, M Penney, et al.
Hormone Research|October 29, 2005
Clinical features, diagnosis and molecular studies of familial central diabetes insipidusJ H Davies, M Penney, A P Abbes, et al.
The Journal of Clinical Endocrinology and Metabolism|March 12, 2003
The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian populationN Jordan, N Williams, J W Gregory, et al.
Pageof 8