Zobrazeno 1 - 10
of 19 775
pro vyhledávání: '"D Steiner"'
Publikováno v:
Journal of Work and Organizational Psychology, Vol 40, Iss 2, Pp 103-118 (2024)
Organizational members may be reluctant to express opinions or concerns because they feel that speaking out is futile. This phenomenon, named “acquiescent silence,” is examined in this paper through the lens of learned helplessness theory. We tes
Externí odkaz:
https://doaj.org/article/b0b9ae8ca6aa4d5786d9b7045c92af54
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundX-linked hypophosphatemic rickets (XLH) is a rare genetic disease characterized by inappropriately elevated circulating fibroblast growth factor 23 (FGF-23) and subsequent urinary phosphate wasting. The primary clinical manifestations of XL
Externí odkaz:
https://doaj.org/article/c643fa210e9947d5a9b30f62ed4a2ccf
Autor:
Garvie, A.F.
Publikováno v:
The Journal of Hellenic Studies, 2011 Jan 01. 131, 171-172.
Externí odkaz:
https://www.jstor.org/stable/41722143
Autor:
Smith, Joseph
Publikováno v:
In Urologic Oncology: Seminars and Original Investigations 2009 27(6):692-693
Autor:
Dirk D. Steiner, Stephen W. Gilliland
Publikováno v:
Justice in the Workplace ISBN: 9781410600301
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffcad3f38cfa53d095d090dcb104cad2
https://doi.org/10.4324/9781410600301-15
https://doi.org/10.4324/9781410600301-15
Autor:
Samuel S. Gidding, Christie M. Ballantyne, Marina Cuchel, Sarah de Ferranti, Lisa Hudgins, Allison Jamison, Mary P. McGowan, Amy L. Peterson, Robert D. Steiner, Melissa K. Uveges, Yunshu Wang
Publikováno v:
Global Heart, Vol 19, Iss 1, Pp 43-43 (2024)
Homozygous familial hypercholesterolemia (HoFH) is an ultra-rare inherited condition that affects approximately one in 300,000 people. The disorder is characterized by extremely high, life-threatening levels of low-density lipoprotein (LDL) cholester
Externí odkaz:
https://doaj.org/article/d2058999a0ea4372bd20514d6dc45bef
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Cerebrotendinous xanthomatosis (CTX) is a rare recessive genetic disease characterized by disruption of bile acid synthesis due to inactivation of the CYP27A1 gene. Treatment is available in the form of bile acid replacement. CTX
Externí odkaz:
https://doaj.org/article/ea2be3e68ba743128073fb3d9cabde54
Publikováno v:
JIMD Reports, Vol 63, Iss 5, Pp 434-445 (2022)
Abstract Hypophosphatasia (HPP) is a genetic condition with broad clinical manifestations caused by alkaline phosphatase (ALP) deficiency. Adults with HPP exhibit a wide spectrum of signs and symptoms. Dental manifestations including premature tooth
Externí odkaz:
https://doaj.org/article/e0be3073fc154120a7553e9e480c7a25
Autor:
Steven J. Fliesler, Robert D. Steiner
Publikováno v:
Journal of Lipid Research, Vol 64, Iss 8, Pp 100421- (2023)
Externí odkaz:
https://doaj.org/article/b193092c4de14f709bdee26330d31807
Autor:
Brian M. Stecher, Michael S. Garet, Laura S. Hamilton, Elizabeth D. Steiner, Abby Robyn, Jeffrey Poirier, Deborah Holtzman, Eleanor S. Fulbeck, Jay Chambers, Iliana Brodziak de los Reyes
To improve the U.S. education system through more-effective classroom teaching, in school year 2009–2010, the Bill and Melinda Gates Foundation announced its Intensive Partnerships for Effective Teaching. Researchers from the RAND Corporation and t