Search research articles
Contact Us
Filters
Showing results (181-190 of 193) with videos related to
Page
of 20
Sort By:
Archives of Disease in Childhood
|
October 1, 1970
Neonatal hypoglycaemia in infants of diabetic mothers given sulphonylurea drugs in pregnancy
M L Kemball, C McIver, R D Milner, et al.
The Journal of Endocrinology
|
March 1, 1983
Increased thymidine incorporation into fetal rat cartilage in vitro in the presence of human somatomedin, epidermal growth factor and other growth factors
D J Hill, A T Holder, J Seid, et al.
Journal of Molecular Endocrinology
|
January 1, 1989
Immunological distribution of one form of insulin-like growth factor (IGF)-binding protein and IGF peptides in human fetal tissues
D J Hill, D R Clemmons, S Wilson, et al.
British Journal of Diseases of the Chest
|
January 1, 1984
Factors affecting the peak expiratory flow rate in children
R A Primhak, J D Biggins, J N Tsanakas, et al.
Endocrinology
|
November 1, 1985
Fetal rat myoblasts release both rat somatomedin-C (SM-C)/insulin-like growth factor I (IGF I) and multiplication-stimulating activity in vitro: partial characterization and biological activity of myoblast-derived SM-C/IGF I
D J Hill, C J Crace, S P Nissley, et al.
The Journal of Endocrinology
|
August 1, 1977
Neonatal islet cell transplantation in the diabetic rat: effect on hepatic enzyme activity and glucose homeostasis
Y Mangnall, A Smythe, D N Slater, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 17, 1998
Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency
F Pernasetti, R D Milner, A A al Ashwal, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
April 1, 1994
Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patient
M A Berg, R Peoples, L Pérez-Jurado, et al.
Pediatric Research
|
November 1, 1984
Reduced plasma somatomedin activity and costal cartilage sulfate incorporation activity during experimental growth retardation in the fetal rat
F A De Prins, D J Hill, M Fekete, et al.
Journal of Medical Genetics
|
November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families
R A Gibson, D Ford, S Jansen, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 193) with videos related to
Sort By:
Page
of 20
Archives of Disease in Childhood
|
October 1, 1970
Neonatal hypoglycaemia in infants of diabetic mothers given sulphonylurea drugs in pregnancy
M L Kemball, C McIver, R D Milner, et al.
The Journal of Endocrinology
|
March 1, 1983
Increased thymidine incorporation into fetal rat cartilage in vitro in the presence of human somatomedin, epidermal growth factor and other growth factors
D J Hill, A T Holder, J Seid, et al.
Journal of Molecular Endocrinology
|
January 1, 1989
Immunological distribution of one form of insulin-like growth factor (IGF)-binding protein and IGF peptides in human fetal tissues
D J Hill, D R Clemmons, S Wilson, et al.
British Journal of Diseases of the Chest
|
January 1, 1984
Factors affecting the peak expiratory flow rate in children
R A Primhak, J D Biggins, J N Tsanakas, et al.
Endocrinology
|
November 1, 1985
Fetal rat myoblasts release both rat somatomedin-C (SM-C)/insulin-like growth factor I (IGF I) and multiplication-stimulating activity in vitro: partial characterization and biological activity of myoblast-derived SM-C/IGF I
D J Hill, C J Crace, S P Nissley, et al.
The Journal of Endocrinology
|
August 1, 1977
Neonatal islet cell transplantation in the diabetic rat: effect on hepatic enzyme activity and glucose homeostasis
Y Mangnall, A Smythe, D N Slater, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 17, 1998
Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency
F Pernasetti, R D Milner, A A al Ashwal, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
April 1, 1994
Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patient
M A Berg, R Peoples, L Pérez-Jurado, et al.
Pediatric Research
|
November 1, 1984
Reduced plasma somatomedin activity and costal cartilage sulfate incorporation activity during experimental growth retardation in the fetal rat
F A De Prins, D J Hill, M Fekete, et al.
Journal of Medical Genetics
|
November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia families
R A Gibson, D Ford, S Jansen, et al.
Page
of 20