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International Journal of Pediatric Endocrinology
|
February 1, 2017
Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in <i>FAM111A</i> gene
Mary B Abraham, Dong Li, Dave Tang, et al.
Nuclear Instruments & Methods in Physics Research. Section A, Accelerators, Spectrometers, Detectors and Associated Equipment
|
December 16, 2014
A New Time Calibration Method for Switched-capacitor-array-based Waveform Samplers
H Kim, C-T Chen, N Eclov, et al.
Cardio-Oncology (London, England)
|
March 11, 2020
Early markers of cardiovascular injury in childhood leukaemia survivors treated with anthracycline chemotherapy
Treya M Long, Channa E Marsh, Lawrence G Dembo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 3, 2014
NNT pseudoexon activation as a novel mechanism for disease in two siblings with familial glucocorticoid deficiency
Tatiana V Novoselova, Shoshana R Rath, Karen Carpenter, et al.
IEEE Transactions on Nuclear Science
|
November 24, 2015
Performance of the Tachyon Time-of-Flight PET Camera
Q Peng, W-S Choong, C Vu, et al.
Journal of Paediatrics and Child Health
|
August 31, 2018
Completeness of protocols for clinical trials in children submitted to ethics committees
Pathma D Joseph, Patrina Hy Caldwell, Elizabeth H Barnes, et al.
Physiological Reports
|
December 5, 2015
Glicentin-related pancreatic polypeptide inhibits glucose-stimulated insulin secretion from the isolated pancreas of adult male rats
Lynda Whiting, Kevin W Stewart, Deborah L Hay, et al.
Clinical Endocrinology
|
September 29, 2011
Growth hormone regimens in Australia: analysis of the first 3 years of treatment for idiopathic growth hormone deficiency and idiopathic short stature
Ian P Hughes, Mark Harris, Catherine S Choong, et al.
Clinical Genetics
|
January 12, 2012
Childhood adrenocortical carcinoma as a sentinel cancer for detecting families with germline TP53 mutations
S S Choong, Z A Latiff, M Mohamed, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 17, 2013
Overexpression of aromatase associated with loss of heterozygosity of the STK11 gene accounts for prepubertal gynecomastia in boys with Peutz-Jeghers syndrome
Seungmin Ham, Sarah J Meachem, Catherine S Choong, et al.
Page
of 16
Search research articles
Search
Showing results (101-110 of 157) with videos related to
Sort By:
Page
of 16
International Journal of Pediatric Endocrinology
|
February 1, 2017
Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in <i>FAM111A</i> gene
Mary B Abraham, Dong Li, Dave Tang, et al.
Nuclear Instruments & Methods in Physics Research. Section A, Accelerators, Spectrometers, Detectors and Associated Equipment
|
December 16, 2014
A New Time Calibration Method for Switched-capacitor-array-based Waveform Samplers
H Kim, C-T Chen, N Eclov, et al.
Cardio-Oncology (London, England)
|
March 11, 2020
Early markers of cardiovascular injury in childhood leukaemia survivors treated with anthracycline chemotherapy
Treya M Long, Channa E Marsh, Lawrence G Dembo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 3, 2014
NNT pseudoexon activation as a novel mechanism for disease in two siblings with familial glucocorticoid deficiency
Tatiana V Novoselova, Shoshana R Rath, Karen Carpenter, et al.
IEEE Transactions on Nuclear Science
|
November 24, 2015
Performance of the Tachyon Time-of-Flight PET Camera
Q Peng, W-S Choong, C Vu, et al.
Journal of Paediatrics and Child Health
|
August 31, 2018
Completeness of protocols for clinical trials in children submitted to ethics committees
Pathma D Joseph, Patrina Hy Caldwell, Elizabeth H Barnes, et al.
Physiological Reports
|
December 5, 2015
Glicentin-related pancreatic polypeptide inhibits glucose-stimulated insulin secretion from the isolated pancreas of adult male rats
Lynda Whiting, Kevin W Stewart, Deborah L Hay, et al.
Clinical Endocrinology
|
September 29, 2011
Growth hormone regimens in Australia: analysis of the first 3 years of treatment for idiopathic growth hormone deficiency and idiopathic short stature
Ian P Hughes, Mark Harris, Catherine S Choong, et al.
Clinical Genetics
|
January 12, 2012
Childhood adrenocortical carcinoma as a sentinel cancer for detecting families with germline TP53 mutations
S S Choong, Z A Latiff, M Mohamed, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 17, 2013
Overexpression of aromatase associated with loss of heterozygosity of the STK11 gene accounts for prepubertal gynecomastia in boys with Peutz-Jeghers syndrome
Seungmin Ham, Sarah J Meachem, Catherine S Choong, et al.
Page
of 16