Zobrazeno 1 - 10
of 141
pro vyhledávání: '"GH: growth hormone"'
Publikováno v:
Journal of Education, Health and Sport, Vol 5, Iss 6, Pp 313-320 (2015)
Habel Angelika, Górecka Milena, Duszyńska-Stolarska Oliwia, Mroczkowski Sławomir. Zmienność genu hormonu wzrostu i jego związek z cechami budowy ciała i użytkowości mięsnej = Variability of growth hormone gene and its association with growt
Externí odkaz:
https://doaj.org/article/5da4202d5d0b415d9765c3f0765797e0
Akademický článek
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Autor:
Nandu Thalange, Hafsa Omer Sulaiman
Publikováno v:
AACE Clinical Case Reports
Objective Pycnodysostosis is commonly associated with growth hormone (GH) deficiency and responds well to GH therapy with achievement of normal or near-normal height and restoration of body proportions. Case Report A 22-month-old extremely short (−
Autor:
Tomoaki Tanaka, Kentaro Horiguchi, Sawako Suzuki, Kazuki Ishiwata, Hanna Deguchi-Horiuchi, Naoko Inoshita, Masanori Fujimoto, Chikako Ohwada, Yasuo Iwadate, Emiko Sakaida, Akiko Ishida, Ichiro Tatsuno, Yutaro Ruike, Kumiko Naito, Hisashi Koide, Jun-ichiro Ikeda, Koutaro Yokote
Publikováno v:
AACE Clinical Case Reports
Objective Intravascular large B-cell lymphoma (IVLBCL) is a rare and aggressive type of B-cell lymphoma with large cells growing within the lumen of blood vessels. Although previous reports revealed highly variable symptoms resulting from small-vesse
Publikováno v:
Mayo Clinic Proceedings: Innovations, Quality & Outcomes, Vol 4, Iss 3, Pp 315-338 (2020)
Mayo Clinic Proceedings: Innovations, Quality & Outcomes
Mayo Clinic Proceedings: Innovations, Quality & Outcomes
An understanding of the molecular basis of liver regeneration will open new horizons for the development of novel therapies for chronic liver failure. Such therapies would solve the drawbacks associated with liver transplant, including the shortage o
Publikováno v:
Journal of Clinical & Translational Endocrinology
Journal of Clinical & Translational Endocrinology, Vol 27, Iss, Pp 100283-(2022)
Journal of Clinical & Translational Endocrinology, Vol 27, Iss, Pp 100283-(2022)
Highlights • Development of CFLD adds significant morbidity and mortality to those with CF. • CFLD is associated with an increased prevalence of endocrinopathies. • Current treatment options for CFLD remain limited. • Early recognition and tr
Autor:
Laura Volpi, Elisa Magnani, Chiara Diazzi, Vincenzo Rochira, Monzani Maria Laura, Simone Pederzoli
Publikováno v:
Endocrine Abstracts.
Autor:
James MacFarlane, Olympia Koulouri, Iosif Mendichovszky, James R. Tysome, Daniel Scoffings, Antia Fernandez-Pombo, Angelos G. Kolias, Thomas Santarius, Richard Mannion, Mark Gurnell, Neil Donnelly, Andrew S Powlson, Russell Senanayake, Andrew J. Martin, Gul Bano, Daniel Gillett, Waiel A Bashari, Heok Cheow
Publikováno v:
Neurosurgical focus. 48(6)
OBJECTIVEThe object of this study was to determine if revision transsphenoidal surgery (TSS), guided by 11C-methionine PET/CT coregistered with volumetric MRI (Met-PET/MRCR), can lead to remission in patients with persistent acromegaly due to a posto
Publikováno v:
Benvenga, S, Klose, M, Vita, R & Feldt-Rasmussen, U 2018, ' Less known aspects of central hypothyroidism : Part 1-Acquired etiologies ', Journal of Clinical and Translational Endocrinology, vol. 14, pp. 25-33 . https://doi.org/10.1016/j.jcte.2018.09.003
Journal of Clinical & Translational Endocrinology
Journal of Clinical & Translational Endocrinology, Vol 14, Iss, Pp 25-33 (2018)
Journal of Clinical & Translational Endocrinology
Journal of Clinical & Translational Endocrinology, Vol 14, Iss, Pp 25-33 (2018)
Central hypothyroidism (CH) is a rare cause of hypothyroidism. CH is frequently overlooked, as its clinical picture is subtle and includes non-specific symptoms; furthermore, if measurement of TSH alone is used to screen for thyroid function, TSH con
Autor:
Martin Bidlingmaier, Birgit Rathkolb, Martin Hrabĕ de Angelis, Arne Hinrichs, Werner F. Blum, Sebastian Bultmann, Heinrich Leonhardt, Maik Dahlhoff, Simone Renner, Andreas Blutke, Eckhard Wolf, Barbara Kessler, Andreas Hoeflich, Hiroshi Nagashima, Maren Bernau, Mayuko Kurome, Rüdiger Wanke, Elisabeth Kemter, Armin M. Scholz
Publikováno v:
Molecular Metabolism, Vol 11, Iss, Pp 113-128 (2018)
Molecular Metabolism
Mol. Metab. 11, 113-128 (2018)
Molecular metabolism, 11: 113-128
Molecular Metabolism
Mol. Metab. 11, 113-128 (2018)
Molecular metabolism, 11: 113-128
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 gener