Biochemical and Clinical Assessments of Segmental Maxillary Posterior Tooth Intrusion

Autor: Jintana Tasanapanont, Tanapan Wattanachai, Janya Apisariyakul, Peraphan Pothacharoen, Siriwan Ongchai, Prachya Kongtawelert, Marit Midtbø, Dhirawat Jotikasthira

Publikováno v: International Journal of Dentistry, Vol 2017 (2017)

Objective. To compare chondroitin sulphate (CS) levels around maxillary second premolars, first molars, and second molars between the unloaded and the loaded periods and to measure the rates of intrusion of maxillary posterior teeth during segmental

Externí odkaz: https://doaj.org/article/4ba90b8726564b6b9dd3be7fac3dd70e

Kraniofaciale og orale senskader etter behandling av barnekreft

Autor: Dorota Malgorzata Wojcik, Tine Birkeland Sivertsen, Sigbjørn Løes, Marit Midtbø

Source at https://www.tannlegetidende.no/journal/2021/5/m-582/Kraniofaciale_og_orale_senskader_etter_behandling_av_barnekreft. Årlig blir ca. 190 norske barn rammet av kreft. Aldersgruppen 0–6 år har den høyeste forekomsten. Leukemier og svulste

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9193901777880cdb5533b2e715f9eafe
https://hdl.handle.net/10037/24027

Etiology-Based Dental and Craniofacial Diagnostics

Autor: Marit Midtbø

Publikováno v: Den norske tannlegeforenings Tidende. 127

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5b3834492e50e7b30b7934798641c5ae
https://doi.org/10.56373/2017-5-22

Interdisciplinary Treatment of Gingival Recession

Autor: Marit, Midtbø, Marte S, Daehlin, Kristin, Hage, Dagmar F, Bunaes, Einar, Berg, Knut N, Leknes

Publikováno v: Journal of clinical orthodontics : JCO. 50(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::93b495678ea3eb80bdc6933e10366dcd
https://pubmed.ncbi.nlm.nih.gov/27017259

Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19

Autor: Heleen H. Arts, Nine V A M Knoers, Machteld M. Oud, Jan-Stephan F. Sanders, Marit Midtbø, Sabine Leh, Marie Matignon, Cécile Jeanpierre, Per M. Knappskog, Dorus A. Mans, Ronald Roepman, Ben C.J. Hamel, Irene Stolte-Dijkstra, Eric J. Steenbergen, Eyvind Rødahl, Cecilie Bredrup, Christian Gilissen, Damien Brackman, Emilie Filhol, Olav H. Haugen, Helge Boman, Rolph Pfundt, Torunn Fiskerstrand, Christine Bole-Feysot, Patrick Nitschké, Joris A. Veltman, Sophie Saunier, Alexander Hoischen

Publikováno v: American Journal of Human Genetics, 89, 5, pp. 634-43
American Journal of Human Genetics, 89, 634-43
The American Journal of Human Genetics; Vol 89
American Journal of Human Genetics, 89(5), 634-643. CELL PRESS

Item does not contain fulltext A subset of ciliopathies, including Sensenbrenner, Jeune, and short-rib polydactyly syndromes are characterized by skeletal anomalies accompanied by multiorgan defects such as chronic renal failure and retinitis pigment

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df8e665acd0725f98f3168560340a2bb
https://doi.org/10.1016/j.ajhg.2011.10.001