M B Ranke|J R Bierich - JoVE Visualize

Showing results (201-210 of 246) with videos related to

Pageof 25

Sort By:

Journal of Medical Genetics|October 21, 2005

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domainT Eggermann, N Schönherr, E Meyer, et al.

Journal of Medical Genetics|May 3, 2005

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?T Eggermann, E Meyer, C Obermann, et al.

Regulatory Peptides|October 27, 1999

Correlation of type I insulin-like growth factor receptor (IGF-I-R) and insulin receptor-related receptor (IRR) messenger RNA levels in tumor cell lines from pediatric tumors of neuronal originM W Elmlinger, U Rauschnabel, E Koscielniak, et al.

Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 1, 1994

Improvement of diagnostic criteria in growth hormone insensitivity syndrome: solutions and pitfalls. Pharmacia Study Group on Insulin-like Growth Factor I Treatment in Growth Hormone Insensitivity SyndromesW F Blum, A M Cotterill, M C Postel-Vinay, et al.

Klinische Padiatrie|November 1, 1991

[Adrenocortical nodular hyperplasia as a cause of Cushing syndrome in the neonatal period]P Gessler, M B Ranke, H Wollmann, et al.

Endocrinology|March 17, 2001

In vivo expression of insulin-like growth factor-binding protein-2 in human gliomas increases with the tumor gradeM W Elmlinger, M H Deininger, B S Schuett, et al.

Clinical Endocrinology|August 31, 2002

The metabolic effects of short-term administration of physiological versus high doses of GH therapy in GH deficient adultsK Yuen, D Cook, K Ong, et al.

Acta Paediatrica (Oslo, Norway : 1992)|December 10, 1998

Bone age in 116 untreated patients with Turner's syndrome rated by a computer-assisted method (CASAS)C P Schwarze, D Arens, H P Haber, et al.

Growth Regulation|March 1, 1993

Clinical studies of IGFBP-2 by radioimmunoassayW F Blum, N Horn, J Kratzsch, et al.

Journal of Molecular Medicine (Berlin, Germany)|November 12, 2005

Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutationsP M Holterhus, R Werner, U Hoppe, et al.

Pageof 25

Showing results (201-210 of 246) with videos related to

Sort By:

Pageof 25

Journal of Medical Genetics|October 21, 2005

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domainT Eggermann, N Schönherr, E Meyer, et al.

Journal of Medical Genetics|May 3, 2005

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?T Eggermann, E Meyer, C Obermann, et al.

Regulatory Peptides|October 27, 1999

Correlation of type I insulin-like growth factor receptor (IGF-I-R) and insulin receptor-related receptor (IRR) messenger RNA levels in tumor cell lines from pediatric tumors of neuronal originM W Elmlinger, U Rauschnabel, E Koscielniak, et al.

Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 1, 1994

Improvement of diagnostic criteria in growth hormone insensitivity syndrome: solutions and pitfalls. Pharmacia Study Group on Insulin-like Growth Factor I Treatment in Growth Hormone Insensitivity SyndromesW F Blum, A M Cotterill, M C Postel-Vinay, et al.

Klinische Padiatrie|November 1, 1991

[Adrenocortical nodular hyperplasia as a cause of Cushing syndrome in the neonatal period]P Gessler, M B Ranke, H Wollmann, et al.

Endocrinology|March 17, 2001

In vivo expression of insulin-like growth factor-binding protein-2 in human gliomas increases with the tumor gradeM W Elmlinger, M H Deininger, B S Schuett, et al.

Clinical Endocrinology|August 31, 2002

The metabolic effects of short-term administration of physiological versus high doses of GH therapy in GH deficient adultsK Yuen, D Cook, K Ong, et al.

Acta Paediatrica (Oslo, Norway : 1992)|December 10, 1998

Bone age in 116 untreated patients with Turner's syndrome rated by a computer-assisted method (CASAS)C P Schwarze, D Arens, H P Haber, et al.

Growth Regulation|March 1, 1993

Clinical studies of IGFBP-2 by radioimmunoassayW F Blum, N Horn, J Kratzsch, et al.

Journal of Molecular Medicine (Berlin, Germany)|November 12, 2005

Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutationsP M Holterhus, R Werner, U Hoppe, et al.

Pageof 25