Search research articles
Contact Us
Filters
Showing results (171-180 of 182) with videos related to
Page
of 19
Sort By:
Pediatric Research
|
March 1, 1989
Defective leukocyte fungicidal activity in end-organ resistance to 1,25-dihydroxyvitamin D
A Etzioni, Z Hochberg, S Pollak, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1996
Clinical, biochemical, and genetic findings in a large pedigree of male and female patients with 5 alpha-reductase 2 deficiency
Z Hochberg, R Chayen, N Reiss, et al.
Nature Genetics
|
April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
B Coyle, R Coffey, J A Armour, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
An ochre mutation in the vitamin D receptor gene causes hereditary 1,25-dihydroxyvitamin D3-resistant rickets in three families
H H Ritchie, M R Hughes, E T Thompson, et al.
Clinical Endocrinology
|
April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome
E Gausden, J A Armour, B Coyle, et al.
Acta Paediatrica Scandinavica. Supplement
|
January 1, 1990
Conclusions: a consensus statement on growth hormone therapy
R Rosenfeld, Z Hochberg, K Albertsson-Wikland, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
August 25, 2009
In vitro fertilisation and use of ovulation enhancers may both influence childhood height in very low birthweight infants
I R Makhoul, A Tamir, D Bader, et al.
Hormone Research
|
February 14, 2004
From bone biology to bone analysis
E Schoenau, G Saggese, F Peter, et al.
Thyroid : Official Journal of the American Thyroid Association
|
October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor
D Tiosano, S Pannain, G Vassart, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
February 23, 2025
Targeted quantitative analysis of urinary bile acids by liquid chromatography-tandem mass spectrometry: Method development and application to healthy and obese children
M Schauermann, R Wang, J Pons-Kuehnemann, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 182) with videos related to
Sort By:
Page
of 19
Pediatric Research
|
March 1, 1989
Defective leukocyte fungicidal activity in end-organ resistance to 1,25-dihydroxyvitamin D
A Etzioni, Z Hochberg, S Pollak, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1996
Clinical, biochemical, and genetic findings in a large pedigree of male and female patients with 5 alpha-reductase 2 deficiency
Z Hochberg, R Chayen, N Reiss, et al.
Nature Genetics
|
April 1, 1996
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
B Coyle, R Coffey, J A Armour, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1989
An ochre mutation in the vitamin D receptor gene causes hereditary 1,25-dihydroxyvitamin D3-resistant rickets in three families
H H Ritchie, M R Hughes, E T Thompson, et al.
Clinical Endocrinology
|
April 1, 1996
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome
E Gausden, J A Armour, B Coyle, et al.
Acta Paediatrica Scandinavica. Supplement
|
January 1, 1990
Conclusions: a consensus statement on growth hormone therapy
R Rosenfeld, Z Hochberg, K Albertsson-Wikland, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
August 25, 2009
In vitro fertilisation and use of ovulation enhancers may both influence childhood height in very low birthweight infants
I R Makhoul, A Tamir, D Bader, et al.
Hormone Research
|
February 14, 2004
From bone biology to bone analysis
E Schoenau, G Saggese, F Peter, et al.
Thyroid : Official Journal of the American Thyroid Association
|
October 19, 1999
The hypothyroidism in an inbred kindred with congenital thyroid hormone and glucocorticoid deficiency is due to a mutation producing a truncated thyrotropin receptor
D Tiosano, S Pannain, G Vassart, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
February 23, 2025
Targeted quantitative analysis of urinary bile acids by liquid chromatography-tandem mass spectrometry: Method development and application to healthy and obese children
M Schauermann, R Wang, J Pons-Kuehnemann, et al.
Page
of 19