Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Katharina Tischlinger"'
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
ObjectivesVitamin D deficiency in neonates can have life-threatening consequences, hence the knowledge of risk factors is essential. This study aimed to explore the effect of maternal socioeconomic status (SES) on newborn 25-hydroxyvitamin D (25OHD)
Externí odkaz:
https://doaj.org/article/09ba76663e044bf5baf530daa8404d7b
Autor:
Rodrigo Montero-Lopez, Elisabeth Laurer, Katharina Tischlinger, Dóra Nagy, Mario Scala, Wolfgang Kranewitter, Gerald Webersinke, Thomas Hörtenhuber, Wolfgang Högler
Publikováno v:
Bone Reports, Vol 16, Iss , Pp 101595- (2022)
Background: Vertebral compression fractures (VFs) are a common and severe finding in patients with osteoporosis. In children, VFs have the unique potential to reshape and regain their original configuration. Spontaneous vertebral body reshaping (i.e.
Externí odkaz:
https://doaj.org/article/a784abd5e1634c7d956c2c6265165c16
Autor:
Ahmed El-Gazzar, Johannes A. Mayr, Barbara Voraberger, Karin Brugger, Stéphane Blouin, Katharina Tischlinger, Hans-Christoph Duba, Holger Prokisch, Nadja Fratzl-Zelman, Wolfgang Högler
Publikováno v:
Bone Reports, Vol 15, Iss , Pp 101110- (2021)
Osteogenesis imperfecta (OI) is an inherited genetic disorder characterized by frequent bone fractures and reduced bone mass. Most cases of OI are caused by dominantly inherited heterozygous mutations in one of the two genes encoding type I collagen,
Externí odkaz:
https://doaj.org/article/bdb0050b07464f549760c469b26f4bb0
Publikováno v:
Journal für Klinische Endokrinologie und Stoffwechsel. 15:105-110
ZusammenfassungDer idiopathische, isolierte Wachstumshormonmangel („idiopathic isolated growth hormone deficiency“, IGHD) ist eine seltene Erkrankung. Die Diagnose wird aufgrund diagnostischer Unschärfen jedoch im Kindesalter zu häufig gestellt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e3cdec49b2b22e649b763e8a5748157
https://doi.org/10.1007/s41969-022-00175-y
https://doi.org/10.1007/s41969-022-00175-y
Autor:
Katharina Tischlinger, Wolfgang Högler
Publikováno v:
Monatsschrift Kinderheilkunde. 170:169-182
ZusammenfassungDie Mineralisation der Wachstumsfuge und des Knochens benötigt suffiziente Mengen an Kalzium und Phosphat, um ein adäquates Körperwachstum und eine adäquate Knochenstärke zu gewährleisten. Bei Mangelzuständen nehmen Härte und S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f9e9b6637048c7b7a7f3fd6a8973ec
https://doi.org/10.1007/s00112-021-01392-6
https://doi.org/10.1007/s00112-021-01392-6
Autor:
Wolfgang Hoegler, Katharina Tischlinger, Jamie Large, Sunia Naseem, William Fraser, Jonathan Tang, Suma Uday
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6f91af5e66cb7afa8bb8600bf514d75
https://doi.org/10.1530/endoabs.85.p7
https://doi.org/10.1530/endoabs.85.p7
Autor:
Elisabeth Laurer, Antonio Sirovina, Alexandra Blaschitz, Katharina Tischlinger, Rodrigo Montero-Lopez, Thomas Hörtenhuber, Marlene Wimleitner, Wolfgang Högler
Publikováno v:
European journal of endocrinology. 187(2)
Objective Children diagnosed with idiopathic isolated growth hormone deficiency (IGHD) are frequently observed to no longer be GH-deficient at a later stage of growth as a result of ‘GHD reversal’. Reevaluation of GH status by stimulation test is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::044238f2b620d9f7d8b9be65e421e43e
https://pubmed.ncbi.nlm.nih.gov/35670597
https://pubmed.ncbi.nlm.nih.gov/35670597
Autor:
Hans-Christoph Duba, Katharina Tischlinger, Barbara Voraberger, Wolfgang Högler, Holger Prokisch, Nadja Fratzl-Zelman, Ahmed El-Gazzar, Stéphane Blouin, Karin Brugger, Johannes A. Mayr
Publikováno v:
Bone Reports
Bone Rep. 15:101110 (2021)
Bone Reports, Vol 15, Iss, Pp 101110-(2021)
Bone Rep. 15:101110 (2021)
Bone Reports, Vol 15, Iss, Pp 101110-(2021)
Osteogenesis imperfecta (OI) is an inherited genetic disorder characterized by frequent bone fractures and reduced bone mass. Most cases of OI are caused by dominantly inherited heterozygous mutations in one of the two genes encoding type I collagen,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80ada73e08e5e633eee7e8a609dc03bc
http://europepmc.org/articles/PMC8339231
http://europepmc.org/articles/PMC8339231
Autor:
Johanna Grünberger, Katharina Tischlinger, Roland Lanzersdorfer, Elisabeth Laurer, Uvistra Naidoo, Wolfgang Högler, Marlene Wimleitner
Publikováno v:
Bone. 144:115834
First line conventional therapy of hypoparathyroidism comprises oral calcium and active vitamin D analogues. This approach may fail to correct hypocalcemia and hyperphosphatemia caused by the absence of parathyroid hormone and carries the risk of lon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce72ed3b3ddd3b4d20129f9c64aa7a09
https://doi.org/10.1016/j.bone.2020.115834
https://doi.org/10.1016/j.bone.2020.115834