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Hormone Research in Paediatrics
|
May 11, 2012
IGF1, IGF1R and SHOX mutation analysis in short children born small for gestational age and short children with normal birth size (idiopathic short stature)
Janina Caliebe, Sander Broekman, Merel Boogaard, et al.
The Journal of Biological Chemistry
|
May 18, 2004
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes
Antonio Marchini, Tiina Marttila, Anja Winter, et al.
Molecular Endocrinology (Baltimore, Md.)
|
December 4, 2004
Structural and functional characteristics of the Val44Met insulin-like growth factor I missense mutation: correlation with effects on growth and development
Adam Denley, Chunxiao C Wang, Kerrie A McNeil, et al.
BMC Pediatrics
|
May 15, 2008
The diagnostic work up of growth failure in secondary health care; an evaluation of consensus guidelines
Floor K Grote, Wilma Oostdijk, Sabine Mpf De Muinck Keizer-Schrama, et al.
Hormone Research in Paediatrics
|
April 3, 2017
Determinants of Advanced Bone Age in Childhood Obesity
Cornelis J de Groot, Adriaan van den Berg, Bart E P B Ballieux, et al.
The Journal of Pediatrics
|
January 13, 2005
Growth hormone (GH) treatment to final height in children with idiopathic short stature: evidence for a dose effect
Jan M Wit, Lyset T M Rekers-Mombarg, Gordon B Cutler, et al.
Hormone Research in Paediatrics
|
April 29, 2010
Adult height in children with growth hormone deficiency: a randomized, controlled, growth hormone dose-response trial
Theo C J Sas, Maria A J de Ridder, Jan M Wit, et al.
Hormone Research in Paediatrics
|
October 27, 2021
Primary Ovarian Failure in Addition to Classical Clinical Features of Coats Plus Syndrome in a Female Carrying 2 Truncating Variants of CTC1
Joel Riquelme, Sanami Takada, Tessa van Dijk, et al.
European Journal of Endocrinology
|
June 3, 2015
STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability
Renata C Scalco, Vivian Hwa, Horacio M Domené, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 9, 2019
Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor
Marie J E Walenkamp, Jasmijn M L Robers, Jan M Wit, et al.
Page
of 22
Search research articles
Search
Showing results (141-150 of 216) with videos related to
Sort By:
Page
of 22
Hormone Research in Paediatrics
|
May 11, 2012
IGF1, IGF1R and SHOX mutation analysis in short children born small for gestational age and short children with normal birth size (idiopathic short stature)
Janina Caliebe, Sander Broekman, Merel Boogaard, et al.
The Journal of Biological Chemistry
|
May 18, 2004
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes
Antonio Marchini, Tiina Marttila, Anja Winter, et al.
Molecular Endocrinology (Baltimore, Md.)
|
December 4, 2004
Structural and functional characteristics of the Val44Met insulin-like growth factor I missense mutation: correlation with effects on growth and development
Adam Denley, Chunxiao C Wang, Kerrie A McNeil, et al.
BMC Pediatrics
|
May 15, 2008
The diagnostic work up of growth failure in secondary health care; an evaluation of consensus guidelines
Floor K Grote, Wilma Oostdijk, Sabine Mpf De Muinck Keizer-Schrama, et al.
Hormone Research in Paediatrics
|
April 3, 2017
Determinants of Advanced Bone Age in Childhood Obesity
Cornelis J de Groot, Adriaan van den Berg, Bart E P B Ballieux, et al.
The Journal of Pediatrics
|
January 13, 2005
Growth hormone (GH) treatment to final height in children with idiopathic short stature: evidence for a dose effect
Jan M Wit, Lyset T M Rekers-Mombarg, Gordon B Cutler, et al.
Hormone Research in Paediatrics
|
April 29, 2010
Adult height in children with growth hormone deficiency: a randomized, controlled, growth hormone dose-response trial
Theo C J Sas, Maria A J de Ridder, Jan M Wit, et al.
Hormone Research in Paediatrics
|
October 27, 2021
Primary Ovarian Failure in Addition to Classical Clinical Features of Coats Plus Syndrome in a Female Carrying 2 Truncating Variants of CTC1
Joel Riquelme, Sanami Takada, Tessa van Dijk, et al.
European Journal of Endocrinology
|
June 3, 2015
STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability
Renata C Scalco, Vivian Hwa, Horacio M Domené, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 9, 2019
Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor
Marie J E Walenkamp, Jasmijn M L Robers, Jan M Wit, et al.
Page
of 22