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Praxis
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September 10, 2009
[Role of complementary medicine in type 1 diabetes mellitus in two Swiss centres]
U A Scheidegger, C E Flück, K Scheidegger, et al.
Molecular and Cellular Endocrinology
|
June 1, 1995
Regulation of human growth hormone-binding protein production by human growth hormone in a hepatoma cell line
P E Mullis, R W Holl, T Lund, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
September 1, 1995
Genetics and molecular biology in short stature
P E Mullis, J Argente, S Amselem, et al.
European Journal of Endocrinology
|
October 3, 2001
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)
C E Flück, J Deladoëy, S Nayak, et al.
Molecular and Cellular Endocrinology
|
April 1, 1991
Regulation of human growth hormone receptor gene expression by human growth hormone in a human hepatoma cell line
P E Mullis, T Lund, M S Patel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 26, 1998
Suprasellar germinomas in childhood and adolescence: diagnostic pitfalls
G P Ramelli, N von der Weid, Z Stanga, et al.
Hormone Research
|
January 1, 1997
Effect of different serum concentrations of growth hormone-binding protein (GHBP) on the regulation of GH receptor/GHBP gene transcription in a human hepatoma cell line
P E Mullis, A Eblé, J K Wagner, et al.
Clinical Endocrinology
|
April 1, 1991
Growth characteristics and response to growth hormone therapy in patients with hypochondroplasia: genetic linkage of the insulin-like growth factor I gene at chromosome 12q23 to the disease in a subgroup of these patients
P E Mullis, M S Patel, P M Brickell, et al.
The Journal of Endocrinology
|
May 16, 2000
Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line
J M Nuoffer, C Flück, J Deladoëy, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 1998
Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C)
C Flück, J Deladoey, K Rutishauser, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 78) with videos related to
Sort By:
Page
of 8
Praxis
|
September 10, 2009
[Role of complementary medicine in type 1 diabetes mellitus in two Swiss centres]
U A Scheidegger, C E Flück, K Scheidegger, et al.
Molecular and Cellular Endocrinology
|
June 1, 1995
Regulation of human growth hormone-binding protein production by human growth hormone in a hepatoma cell line
P E Mullis, R W Holl, T Lund, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
September 1, 1995
Genetics and molecular biology in short stature
P E Mullis, J Argente, S Amselem, et al.
European Journal of Endocrinology
|
October 3, 2001
Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II)
C E Flück, J Deladoëy, S Nayak, et al.
Molecular and Cellular Endocrinology
|
April 1, 1991
Regulation of human growth hormone receptor gene expression by human growth hormone in a human hepatoma cell line
P E Mullis, T Lund, M S Patel, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 26, 1998
Suprasellar germinomas in childhood and adolescence: diagnostic pitfalls
G P Ramelli, N von der Weid, Z Stanga, et al.
Hormone Research
|
January 1, 1997
Effect of different serum concentrations of growth hormone-binding protein (GHBP) on the regulation of GH receptor/GHBP gene transcription in a human hepatoma cell line
P E Mullis, A Eblé, J K Wagner, et al.
Clinical Endocrinology
|
April 1, 1991
Growth characteristics and response to growth hormone therapy in patients with hypochondroplasia: genetic linkage of the insulin-like growth factor I gene at chromosome 12q23 to the disease in a subgroup of these patients
P E Mullis, M S Patel, P M Brickell, et al.
The Journal of Endocrinology
|
May 16, 2000
Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line
J M Nuoffer, C Flück, J Deladoëy, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 1998
Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C)
C Flück, J Deladoey, K Rutishauser, et al.
Page
of 8