Search research articles
Contact Us
Filters
Showing results (21-30 of 55) with videos related to
Page
of 6
Sort By:
Paediatrics & Child Health
|
February 28, 2015
Managing type 1 diabetes in school: Recommendations for policy and practice
Sarah E Lawrence, Elizabeth A Cummings, Danièle Pacaud, et al.
International Journal of Endocrinology
|
May 22, 2012
Generation of transplantable Beta cells for patient-specific cell therapy
Xiaojie Wang, Daniel L Metzger, Mark Meloche, et al.
JIMD Reports
|
February 5, 2017
Hypogonadotropic Hypogonadism in Males with Glycogen Storage Disease Type 1
Evelyn M Wong, Anna Lehman, Philip Acott, et al.
Nature Reviews. Endocrinology
|
May 7, 2025
Individualized and innovative gender healthcare for transgender and nonbinary youth
Drew B A Clark, Daniel L Metzger, Ken C Pang, et al.
Hormone Research in Paediatrics
|
July 18, 2013
Occurrence of slipped capital femoral epiphysis in children undergoing gonadotropin-releasing hormone agonist therapy for the treatment of central precocious puberty
Mark Inman, Brenden E Hursh, Arati Mokashi, et al.
Pediatric Radiology
|
May 14, 2011
Novel use of F-DOPA PET/CT imaging in a child with paraganglioma/pheochromocytoma syndrome
Daniel S Levine, Daniel L Metzger, Helen R Nadel, et al.
Human Mutation
|
November 21, 2002
GCK and HNF1A mutations in Canadian families with maturity onset diabetes of the young (MODY)
Henian Cao, Sanam Shorey, John Robinson, et al.
Paediatrics & Child Health
|
January 15, 2014
Canadian Pediatric Endocrine Group extension to WHO growth charts: Why bother?
Sarah Lawrence, Elizabeth Cummings, Jean-Pierre Chanoine, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
June 4, 2026
Stability of Transgender Identity in Adolescents Seen in Mutlidisciplinary Specialized Gender Centers: A Mulitcenter Study in Canada
Daniel L Metzger, Arati Mokashi, Danièle Pacaud, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 15, 2014
Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization
Dong Li, Evan E Opas, Florin Tuluc, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 55) with videos related to
Sort By:
Page
of 6
Paediatrics & Child Health
|
February 28, 2015
Managing type 1 diabetes in school: Recommendations for policy and practice
Sarah E Lawrence, Elizabeth A Cummings, Danièle Pacaud, et al.
International Journal of Endocrinology
|
May 22, 2012
Generation of transplantable Beta cells for patient-specific cell therapy
Xiaojie Wang, Daniel L Metzger, Mark Meloche, et al.
JIMD Reports
|
February 5, 2017
Hypogonadotropic Hypogonadism in Males with Glycogen Storage Disease Type 1
Evelyn M Wong, Anna Lehman, Philip Acott, et al.
Nature Reviews. Endocrinology
|
May 7, 2025
Individualized and innovative gender healthcare for transgender and nonbinary youth
Drew B A Clark, Daniel L Metzger, Ken C Pang, et al.
Hormone Research in Paediatrics
|
July 18, 2013
Occurrence of slipped capital femoral epiphysis in children undergoing gonadotropin-releasing hormone agonist therapy for the treatment of central precocious puberty
Mark Inman, Brenden E Hursh, Arati Mokashi, et al.
Pediatric Radiology
|
May 14, 2011
Novel use of F-DOPA PET/CT imaging in a child with paraganglioma/pheochromocytoma syndrome
Daniel S Levine, Daniel L Metzger, Helen R Nadel, et al.
Human Mutation
|
November 21, 2002
GCK and HNF1A mutations in Canadian families with maturity onset diabetes of the young (MODY)
Henian Cao, Sanam Shorey, John Robinson, et al.
Paediatrics & Child Health
|
January 15, 2014
Canadian Pediatric Endocrine Group extension to WHO growth charts: Why bother?
Sarah Lawrence, Elizabeth Cummings, Jean-Pierre Chanoine, et al.
The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine
|
June 4, 2026
Stability of Transgender Identity in Adolescents Seen in Mutlidisciplinary Specialized Gender Centers: A Mulitcenter Study in Canada
Daniel L Metzger, Arati Mokashi, Danièle Pacaud, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 15, 2014
Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization
Dong Li, Evan E Opas, Florin Tuluc, et al.
Page
of 6