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Roland Pfäffle

Showing results (51-60 of 69) with videos related to

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Eclinicalmedicine|August 13, 2021
Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference valuesElena 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 retardationDenise 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 StudyRoland 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 PhenylketonuriaAlena 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 StudiesTilman 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 statureEva-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 effectGuntram 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 studyConstanze 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 retardationM Jennifer Abuzzahab, Anke Schneider, Audrey Goddard, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Eclinicalmedicine|August 13, 2021
Dynamic alterations in linear growth and endocrine parameters in children with obesity and height reference valuesElena 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 retardationDenise 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 StudyRoland 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 PhenylketonuriaAlena 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 StudiesTilman 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 statureEva-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 effectGuntram 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 studyConstanze 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 retardationM Jennifer Abuzzahab, Anke Schneider, Audrey Goddard, et al.
Pageof 7