Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mathisen, Linda"'
Autor:
Kristensen, Erle1,2 (AUTHOR), Mathisen, Linda3 (AUTHOR), Berland, Siren4 (AUTHOR), Klingenberg, Claus5,6 (AUTHOR), Brodtkorb, Eylert7,8 (AUTHOR), Rasmussen, Magnhild9,10 (AUTHOR), Tangeraas, Trine11,12 (AUTHOR), Bliksrud, Yngve T.1 (AUTHOR), Rahman, Shamima12,13,14 (AUTHOR), Bindoff, Laurence Albert11,12,15 (AUTHOR), Hikmat, Omar2,11,12,16 (AUTHOR) omar.hikmat@uib.no
Publikováno v:
Annals of Clinical & Translational Neurology. Jul2024, Vol. 11 Issue 7, p1819-1830. 12p.
Autor:
Slavotinek, Anne, Misceo, Doriana, Htun, Stephanie, Mathisen, Linda, Frengen, Eirik, Foreman, Michelle, Hurtig, Jennifer E., Enyenihi, Liz, Sterrett, Maria C., Leung, Sara W., Schneidman-Duhovny, Dina, Estrada-Veras, Juvianee, Duncan, Jacque L., Haaxma, Charlotte A., Kamsteeg, Erik-Jan, Xia, Vivian, Beleford, Daniah, Si, Yue, Douglas, Ganka, Treidene, Hans Einar, van Hoof, Ambro, Fasken, Milo B., Corbett, Anita H.
Publikováno v:
Slavotinek, Anne Misceo, Doriana Htun, Stephanie Mathisen, Linda Frengen, Eirik Foreman, Michelle Hurtig, Jennifer E. Enyenihi, Liz Sterrett, Maria C. Leung, Sara W. Schneidman-Duhovny, Dina Estrada-Veras, Juvianee Duncan, Jacque L. Haaxma, Charlotte A. Kamsteeg, Erik-Jan Xia, Vivian Beleford, Daniah Si, Yue Douglas, Ganka Treidene, Hans Einar van Hoof, Ambro Fasken, Milo B. Corbett, Anita H. . Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness. Human Molecular Genetics. 2020, 29(13), 2218-2239
Human Molecular Genetics
Human Molecular Genetics
Autor:
Torgersen, Kristin Stensland, Ho, Thanh Thao Thi, Mathisen, Linda, Slagstad, Ketil, Sem, Marthe, Irgens, Christoffer
Publikováno v:
Torgersen, Kristin Stensland, , , , , Ho, Thanh Thao Thi, , , , , Mathisen, Linda, , , , , Slagstad, Ketil, , , , , Sem, Marthe, , , , , Irgens, Christoffer, , , , , . Tai Chi som fallprofylaktisk tiltak for hjemmeboende eldre over 65 år. Prosjektoppgave, University of Oslo, 2010
Autor:
Mathisen, Linda
Publikováno v:
Mathisen, Linda. In utero eksponering for psykofarmaka i første trimester og risiko for medfødte malformasjoner. Prosjektoppgave, University of Oslo, 2010
Externí odkaz:
http://hdl.handle.net/10852/29632
https://www.duo.uio.no/bitstream/handle/10852/29632/2/prosjekt-Mathisen.pdf
https://www.duo.uio.no/bitstream/handle/10852/29632/2/prosjekt-Mathisen.pdf
Objective: The purpose of this study was to find out how screening and referring arrangements of patients with malocclusions was working between different dental professional groups in the public dental health services in Troms County. We also wanted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f8b4def32a24f46f0bf252038143456a
https://hdl.handle.net/10037/4197
https://hdl.handle.net/10037/4197
Autor:
Slavotinek A; Department of Pediatrics, University of California, San Francisco, CA 94143, USA., Misceo D; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo 0450, Norway., Htun S; Department of Pediatrics, University of California, San Francisco, CA 94143, USA., Mathisen L; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo 0450, Norway., Frengen E; Department of Medical Genetics, Oslo University Hospital and University of Oslo, Oslo 0450, Norway., Foreman M; Department of Microbiology and Molecular Genetics, University of Texas Health Science Center-Houston, Houston, TX 77030, USA., Hurtig JE; Department of Microbiology and Molecular Genetics, University of Texas Health Science Center-Houston, Houston, TX 77030, USA., Enyenihi L; Department of Biology, Emory University, Atlanta, GA 30322, USA., Sterrett MC; Department of Biology, Emory University, Atlanta, GA 30322, USA., Leung SW; Department of Biology, Emory University, Atlanta, GA 30322, USA., Schneidman-Duhovny D; School of Computer Science and Engineering and the Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem 91904, Israel., Estrada-Veras J; Department of Pediatrics-Medical Genetics and Metabolism, Uniformed Services University/Walter Reed NMMC Bethesda, MD 20889, USA., Duncan JL; Department of Ophthalmology, University of California, San Francisco, CA 94143, USA., Haaxma CA; Department of Pediatric Neurology, Amalia Children's Hospital and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen 6500 HB, The Netherlands., Kamsteeg EJ; Department of Human Genetics, Radboud University Medical Center, Nijmegen 6500 HB, The Netherlands., Xia V; Department of Pediatrics, University of California, San Francisco, CA 94143, USA., Beleford D; Department of Pediatrics, University of California, San Francisco, CA 94143, USA., Si Y; GeneDx Inc., MD 20877, USA., Douglas G; GeneDx Inc., MD 20877, USA., Treidene HE; Department of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo 0450, Norway., van Hoof A; Department of Microbiology and Molecular Genetics, University of Texas Health Science Center-Houston, Houston, TX 77030, USA., Fasken MB; Department of Biology, Emory University, Atlanta, GA 30322, USA., Corbett AH; Department of Biology, Emory University, Atlanta, GA 30322, USA.
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2020 Aug 03; Vol. 29 (13), pp. 2218-2239.