Search research articles
Contact Us
Filters
Showing results (121-130 of 249) with videos related to
Page
of 25
Sort By:
European Journal of Pediatrics
|
May 14, 1998
De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
G G Massa, G Binder, W Oostdijk, et al.
Pediatric Diabetes
|
March 16, 2004
Varying clinical presentations at onset of type 1 diabetes mellitus in children--epidemiological evidence for different subtypes of the disease?
A Neu, S Ehehalt, A Willasch, et al.
European Journal of Endocrinology
|
April 16, 1998
Elevated insulin-like growth factor (IGF) binding protein (IGFBP)-2 and IGFBP-4 expression of leukemic T-cells is affected by autocrine/paracrine IGF-II action but not by IGF type I receptor expression
M W Elmlinger, M S Sanatani, M Bell, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 1, 1991
Short-term changes in serum insulin-like growth factors (IGF) and IGF binding protein 3 after different modes of intravenous growth hormone (GH) exposure in GH-deficient patients
J O Jørgensen, W F Blum, N Møller, et al.
Annales De Genetique
|
August 6, 1999
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely
K Eggermann, H A Wollmann, G Binder, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
April 2, 1999
Final height in idiopathic growth hormone deficiency: the KIGS experience. KIGS International Board
W Cutfield, A Lindberg, K Albertsson Wikland, et al.
Journal of Medical Genetics
|
January 11, 2000
Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status
S Mergenthaler, K Eggermann, J Tomiuk, et al.
Scientific Reports
|
April 17, 2022
Accuracy and self-validation of automated bone age determination
D D Martin, A D Calder, M B Ranke, et al.
Human Heredity
|
June 12, 1999
Screening for mutations in the promoter and the coding region of the IGFBP1 and IGFBP3 genes in Silver-Russell syndrome patients
K Eggermann, H A Wollmann, J Tomiuk, et al.
Hormone Research
|
March 22, 2000
Influence of IGF-I and cell density on MDR1 expression in the T-lymphoblastoid cell line CCRF-CEM
C P Schwarze, S Neu, J Beck, et al.
Page
of 25
Search research articles
Search
Showing results (121-130 of 249) with videos related to
Sort By:
Page
of 25
European Journal of Pediatrics
|
May 14, 1998
De novo mutations of the growth hormone gene: an important cause of congenital isolated growth hormone deficiency?
G G Massa, G Binder, W Oostdijk, et al.
Pediatric Diabetes
|
March 16, 2004
Varying clinical presentations at onset of type 1 diabetes mellitus in children--epidemiological evidence for different subtypes of the disease?
A Neu, S Ehehalt, A Willasch, et al.
European Journal of Endocrinology
|
April 16, 1998
Elevated insulin-like growth factor (IGF) binding protein (IGFBP)-2 and IGFBP-4 expression of leukemic T-cells is affected by autocrine/paracrine IGF-II action but not by IGF type I receptor expression
M W Elmlinger, M S Sanatani, M Bell, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 1, 1991
Short-term changes in serum insulin-like growth factors (IGF) and IGF binding protein 3 after different modes of intravenous growth hormone (GH) exposure in GH-deficient patients
J O Jørgensen, W F Blum, N Møller, et al.
Annales De Genetique
|
August 6, 1999
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely
K Eggermann, H A Wollmann, G Binder, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
April 2, 1999
Final height in idiopathic growth hormone deficiency: the KIGS experience. KIGS International Board
W Cutfield, A Lindberg, K Albertsson Wikland, et al.
Journal of Medical Genetics
|
January 11, 2000
Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting status
S Mergenthaler, K Eggermann, J Tomiuk, et al.
Scientific Reports
|
April 17, 2022
Accuracy and self-validation of automated bone age determination
D D Martin, A D Calder, M B Ranke, et al.
Human Heredity
|
June 12, 1999
Screening for mutations in the promoter and the coding region of the IGFBP1 and IGFBP3 genes in Silver-Russell syndrome patients
K Eggermann, H A Wollmann, J Tomiuk, et al.
Hormone Research
|
March 22, 2000
Influence of IGF-I and cell density on MDR1 expression in the T-lymphoblastoid cell line CCRF-CEM
C P Schwarze, S Neu, J Beck, et al.
Page
of 25