Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Stéphane Blouin"'
Autor:
Spela Stunf Pukl, Martin Kronschläger, Manuel Ruiss, Stéphane Blouin, Emre Rüştü Akcan, Oliver Findl
Publikováno v:
BMC Ophthalmology, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Purpose To measure the dislocation forces in relation to haptic material, flange size and needle used. Setting Hanusch Hospital, Vienna, Austria. Design Laboratory Investigation. Methods, main outcome measures 30 G (gauge) thin wall and 27 G
Externí odkaz:
https://doaj.org/article/0fb3d5adf7044a80a8bc7ab2022ea08d
Autor:
Barbara Voraberger, Johannes A. Mayr, Nadja Fratzl-Zelman, Stéphane Blouin, Suma Uday, Robert Kopajtich, Marijke Koedam, Helena Hödlmayr, Saskia B. Wortmann, Bernhard Csillag, Holger Prokisch, Bram C. J. van der Eerden, Ahmed El-Gazzar, Wolfgang Högler
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Bi-allelic variants in ASCC1 cause the ultrarare bone fragility disorder “spinal muscular atrophy with congenital bone fractures-2” (SMABF2). However, the mechanism by which ASCC1 dysfunction leads to this musculoskeletal condition and the nature
Externí odkaz:
https://doaj.org/article/4a17473717f247b2b3e96b896af55a6c
Autor:
Alexandra Tits, Erwan Plougonven, Stéphane Blouin, Markus A. Hartmann, Jean-François Kaux, Pierre Drion, Justin Fernandez, G. Harry van Lenthe, Davide Ruffoni
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021)
Abstract The enthesis allows the insertion of tendon into bone thanks to several remarkable strategies. This complex and clinically relevant location often features a thin layer of fibrocartilage sandwiched between tendon and bone to cope with a high
Externí odkaz:
https://doaj.org/article/6644b3e664df4f29af5264f6ad7e9385
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
Autor:
Riikka E. Mäkitie, Stéphane Blouin, Ville‐Valtteri Välimäki, Sandra Pihlström, Kirsi Määttä, Minna Pekkinen, Nadja Fratzl‐Zelman, Outi Mäkitie, Markus A. Hartmann
Publikováno v:
JBMR Plus, Vol 5, Iss 11, Pp n/a-n/a (2021)
Abstract Pathological variants in SGMS2, encoding sphingomyelin synthase 2 (SMS2), result in a rare autosomal dominant skeletal disorder with cranial doughnut lesions. The disease manifests as early‐onset osteoporosis or a more severe skeletal dysp
Externí odkaz:
https://doaj.org/article/acebc817b0f14b70aa54dc378913b30f
Autor:
Benjamin Hadzimuratovic, Judith Haschka, Markus A Hartmann, Stéphane Blouin, Nadja Fratzl‐Zelman, Jochen Zwerina, Roland Kocijan
Publikováno v:
JBMR Plus, Vol 5, Iss 6, Pp n/a-n/a (2021)
ABSTRACT Tenofovir is a nucleotide analog reverse‐transcriptase inhibitor (NtARTI) used for treatment of chronic hepatitis B and human immunodeficiency virus (HIV). Fanconi syndrome (FS) is a condition affecting the proximal tubules of the kidney,
Externí odkaz:
https://doaj.org/article/2a4b1b40583641ad878deda67581bd4c
Autor:
Gali Guterman-Ram, Ghazal Hedjazi, Chris Stephan, Stéphane Blouin, Jochen Zwerina, Kenneth M. Kozloff, Nadja Fratzl-Zelman, Joan C. Marini
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 100805- (2021)
Externí odkaz:
https://doaj.org/article/a45a9a8a355d4c069d4e835dad533cbf
Autor:
Ghazal Hedjazi, Gali Guterman-Ram, Stéphane Blouin, Markus A. Hartmann, Victoria Schemenz, Wolfgang Wagermaier, Peter Fratzl, Jochen Zwerina, Nadja Fratzl-Zelman, Joan C. Marini
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 100806- (2021)
Externí odkaz:
https://doaj.org/article/e51114a5e5d746f1a7e3ff69b6106ae3
Autor:
Stéphane Blouin, Barbara M. Misof, Markus A. Hartmann, Andrea Berzlanovich, Gerlinde M. Gruber, Sonja Lueger, Phaedra Messmer, Petra Keplinger, Paul Roschger
Publikováno v:
Bone Reports, Vol 13, Iss , Pp 100675- (2020)
Externí odkaz:
https://doaj.org/article/945659bb1cad4e789b95f4dfbf077475
Autor:
Gali Guterman-Ram, Ghazal Hedjazi, Chris Stephan, Stéphane Blouin, Paul Roschger, Klaus Klaushofer, Jochen Zwerina, Kenneth M. Kozloff, Nadja Fratzl-Zelman, Joan C. Marini
Publikováno v:
Bone Reports, Vol 13, Iss , Pp 100650- (2020)
Externí odkaz:
https://doaj.org/article/e86fe0bcedb1451fae44b9cee29bd749