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Eclinicalmedicine
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August 13, 2021
Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values
Elena Kempf, Mandy Vogel, Tim Vogel, et al.
European Journal of Endocrinology
|
November 8, 2018
A new p.(Ile66Serfs*93) IGF2 variant is associated with pre- and postnatal growth retardation
Denise Rockstroh, Heike Pfäffle, Diana Le Duc, et al.
Hormone Research in Paediatrics
|
August 20, 2020
Safety and Effectiveness of Omnitrope®, a Biosimilar Recombinant Human Growth Hormone: More Than 10 Years' Experience from the PATRO Children Study
Roland Pfäffle, Martin Bidlingmaier, Ilonka Kreitschmann-Andermahr, et al.
Hormone Research in Paediatrics
|
September 11, 2018
Growth Hormone Treatment for Short Stature in the USA, Germany and France: 15 Years of Surveillance in the Genetics and Neuroendocrinology of Short-Stature International Study (GeNeSIS)
Roland Pfäffle, Christof Land, Eckhard Schönau, et al.
Pediatrics
|
November 2, 2017
Growth and Final Height Among Children With Phenylketonuria
Alena G Thiele, Ruth Gausche, Cornelia Lindenberg, et al.
Hormone Research in Paediatrics
|
March 6, 2019
Needle-Free and Needle-Based Growth Hormone Therapy in Children: A Pooled Analysis of Three Long-Term Observational Studies
Tilman R Rohrer, Sabine Ceplis-Kastner, Norbert Jorch, et al.
Hormone Research in Paediatrics
|
December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short stature
Eva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 5, 2004
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect
Guntram Borck, A Kemal Topaloglu, Eckhard Korsch, et al.
Therapeutic Advances in Endocrinology and Metabolism
|
October 7, 2024
Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study
Constanze Lämmer, Philippe Backeljauw, Maite Tauber, et al.
The New England Journal of Medicine
|
December 6, 2003
IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation
M Jennifer Abuzzahab, Anke Schneider, Audrey Goddard, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 69) with videos related to
Sort By:
Page
of 7
Eclinicalmedicine
|
August 13, 2021
Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference values
Elena Kempf, Mandy Vogel, Tim Vogel, et al.
European Journal of Endocrinology
|
November 8, 2018
A new p.(Ile66Serfs*93) IGF2 variant is associated with pre- and postnatal growth retardation
Denise Rockstroh, Heike Pfäffle, Diana Le Duc, et al.
Hormone Research in Paediatrics
|
August 20, 2020
Safety and Effectiveness of Omnitrope®, a Biosimilar Recombinant Human Growth Hormone: More Than 10 Years' Experience from the PATRO Children Study
Roland Pfäffle, Martin Bidlingmaier, Ilonka Kreitschmann-Andermahr, et al.
Hormone Research in Paediatrics
|
September 11, 2018
Growth Hormone Treatment for Short Stature in the USA, Germany and France: 15 Years of Surveillance in the Genetics and Neuroendocrinology of Short-Stature International Study (GeNeSIS)
Roland Pfäffle, Christof Land, Eckhard Schönau, et al.
Pediatrics
|
November 2, 2017
Growth and Final Height Among Children With Phenylketonuria
Alena G Thiele, Ruth Gausche, Cornelia Lindenberg, et al.
Hormone Research in Paediatrics
|
March 6, 2019
Needle-Free and Needle-Based Growth Hormone Therapy in Children: A Pooled Analysis of Three Long-Term Observational Studies
Tilman R Rohrer, Sabine Ceplis-Kastner, Norbert Jorch, et al.
Hormone Research in Paediatrics
|
December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short stature
Eva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 5, 2004
Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect
Guntram Borck, A Kemal Topaloglu, Eckhard Korsch, et al.
Therapeutic Advances in Endocrinology and Metabolism
|
October 7, 2024
Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study
Constanze Lämmer, Philippe Backeljauw, Maite Tauber, et al.
The New England Journal of Medicine
|
December 6, 2003
IGF-I receptor mutations resulting in intrauterine and postnatal growth retardation
M Jennifer Abuzzahab, Anke Schneider, Audrey Goddard, et al.
Page
of 7