Zobrazeno 1 - 10
of 332
pro vyhledávání: '"Werner F Blum"'
Autor:
Werner F Blum, Abdullah Alherbish, Afaf Alsagheir, Ahmed El Awwa, Walid Kaplan, Ekaterina Koledova, Martin O Savage
Publikováno v:
Endocrine Connections, Vol 7, Iss 6, Pp R212-R222 (2018)
The growth hormone (GH)–insulin-like growth factor (IGF)-I axis is a key endocrine mechanism regulating linear growth in children. While paediatricians have a good knowledge of GH secretion and assessment, understanding and use of measurements of t
Externí odkaz:
https://doaj.org/article/76c92ffe12024ec18f7a1c15f179abbe
Autor:
Werner F. Blum, Jürgen Klammt, Serge Amselem, Heike M. Pfäffle, Marie Legendre, Marie-Laure Sobrier, Marie-Pierre Luton, Christopher J. Child, Christine Jones, Alan G. Zimmermann, Charmian A. Quigley, Gordon B. Cutler, Jr, Cheri L. Deal, Jan Lebl, Ron G. Rosenfeld, John S. Parks, Roland W. Pfäffle
Publikováno v:
EBioMedicine, Vol 36, Iss , Pp 390-400 (2018)
Background: Pituitary development and GH secretion are orchestrated by multiple genes including GH1, GHRHR, GLI2, HESX1, LHX3, LHX4, PROP1, POU1F1, and SOX3. We aimed to assess their mutation frequency and clinical relevance in children with severe G
Externí odkaz:
https://doaj.org/article/eb38d45a2af84fb1a420e9f01ae4ca4c
Autor:
Arne Hinrichs, Barbara Kessler, Mayuko Kurome, Andreas Blutke, Elisabeth Kemter, Maren Bernau, Armin M. Scholz, Birgit Rathkolb, Simone Renner, Sebastian Bultmann, Heinrich Leonhardt, Martin Hrabĕ de Angelis, Hiroshi Nagashima, Andreas Hoeflich, Werner F. Blum, Martin Bidlingmaier, Rüdiger Wanke, Maik Dahlhoff, Eckhard Wolf
Publikováno v:
Molecular Metabolism, Vol 11, Iss , Pp 113-128 (2018)
Objective: Laron syndrome (LS) is a rare, autosomal recessive disorder in humans caused by loss-of-function mutations of the growth hormone receptor (GHR) gene. To establish a large animal model for LS, pigs with GHR knockout (KO) mutations were gene
Externí odkaz:
https://doaj.org/article/7c74c35d25ac486abfdbf53fba4fa634
Autor:
Werner F Blum, Michael B Ranke, Eberhard Keller, Alexandra Keller, Sandra Barth, Christiaan de Bruin, Stefan A Wudy, Jan M Wit
Publikováno v:
Journal of the Endocrine Society, 6(7). ENDOCRINE SOC
Context Prediction of adult height (AH) is important in clinical management of short children. The conventional methods of Bayley-Pinneau (BP) or Roche-Wainer-Thissen (RWT) have limitations. Objective We aimed to develop a set of algorithms for AH pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::126acd476c6bc0053154aa99328dda7b
http://hdl.handle.net/1887/3575996
http://hdl.handle.net/1887/3575996
Autor:
Verena Behringer, Stefan Wudy, Werner F. Blum, Jeroen M. G. Stevens, Thomas Remer, Christophe Boesch, Gottfried Hohmann
Publikováno v:
Frontiers in Endocrinology, Vol 7 (2016)
There is increasing interest in the characterization of normative senescence in humans. To assess to what extent aging patterns in humans are unique, comparative data from closely-related species, such as non-human primates, can be very useful. Here
Externí odkaz:
https://doaj.org/article/b7a544353e9e41618c6bc0e12bf8c149
Autor:
Robin S. Scott, Charmian A. Quigley, Sreekumar G Pillai, Ying Grace Li, John S. Parks, Milton R. Brown, Poulabi Banerjee, Werner F. Blum
Publikováno v:
Hormone Research in Paediatrics. 91:164-174
Background/Aims: The term idiopathic short stature (ISS) describes short stature of unknown, but likely polygenic, etiology. This study aimed to identify genetic polymorphisms associated with the ISS phenotype, and with growth response to supplementa
Autor:
Andrej Suchomlinov, Sylvia Kirchengast, Raja Chakraborty, Sylwia Bartkowiak, Slawomir Koziel, Robert M. Malina, Lidia Lebedeva, Takashi Satake, Egle Marija Jakimaviciene, Daniel Franken, Christiane Scheffler, Michael Hermanussen, Detlef Groth, Aleksandra Gomula, Jan M. Konarski, James M. Swanson, Ramune Cepuliene, Yehuda Limony, Lidia Martin, Werner F. Blum, Natalia Nowak-Szczepanska, Bárbara Navazo, Vsevolod Konstantinov, Janina Tutkuviene, Anna Apanasewicz, Annang G. Moelyo, James G. Waxmonsky
Publikováno v:
Human biology and public health, Potsdam : Potsdam University Library; University Press, 2021, vol. 1, p. 1-13
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
Twenty-three scientists met at Krobielowice, Poland to discuss the role of growth, nutrition and economy on body size. Contrasting prevailing concepts, re-analyses of studies in Indonesian and Guatemalan school children with high prevalence of stunti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b2fc4bc70c7cda86aedaf06a2ee5f8d
http://sedici.unlp.edu.ar/handle/10915/143660
http://sedici.unlp.edu.ar/handle/10915/143660
Publikováno v:
Journal of the Endocrine Society. 5
Context We hypothesize, based on the degree of residual hypothalamic-pituitary function, that some, but not all, children with growth hormone deficiency (GHD) may have beneficial growth responses to the orally administered growth hormone (GH) secreta
Autor:
Heike Vollbach, Shlomit Shalitin, Ingrid Körber, Marianna Beghini, Katja Kohlsdorf, Werner F. Blum, Julia von Schnurbein, Belinda Lennerz, Ferruccio Santini, Martin Wabitsch, Christian Denzer, Stephanie Brandt
Publikováno v:
International Journal of Obesity (2005)
Background Evidence from in vitro and rodent studies suggests that leptin, a key signal of long-term energy reserves, promotes IGF1 synthesis and linear growth. This effect of leptin has not been fully investigated in humans. The aim of our study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3956f8330824c65d7c393780a70b46f6
http://hdl.handle.net/11568/1115590
http://hdl.handle.net/11568/1115590
Autor:
Michael O. Thorner, Haiying Chen, John C. McKew, George M Bright, Minh-Ha T Do, Werner F. Blum
Publikováno v:
Journal of the Endocrine Society
Context Recombinant human growth hormone (rhGH) is approved for treatment of pediatric growth hormone deficiency (GHD), with greatest growth responses observed in those with severe GHD. Orally administered GH secretagogues (GHS) may be useful treatme