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Page 1
Healthcare databases in Europe for studying medicine use and safety during pregnancy.
Charlton RA, Neville AJ, Jordan S, Pierini A, Damase-Michel C, Klungsøyr K, Andersen AM, Hansen AV, Gini R, Bos JH, Puccini A, Hurault-Delarue C, Brooks CJ, de Jong-van den Berg LT, de Vries CS. Charlton RA, et al. Among authors: klungsoyr k. Pharmacoepidemiol Drug Saf. 2014 Jun;23(6):586-94. doi: 10.1002/pds.3613. Epub 2014 Mar 24. Pharmacoepidemiol Drug Saf. 2014. PMID: 24664855
Comparative Safety of Antiseizure Medication Monotherapy for Major Malformations.
Cohen JM, Alvestad S, Cesta CE, Bjørk MH, Leinonen MK, Nørgaard M, Einarsdóttir K, Engeland A, Gissler M, Karlstad Ø, Klungsøyr K, Odsbu I, Reutfors J, Selmer RM, Tomson T, Ulrichsen SP, Zoega H, Furu K. Cohen JM, et al. Among authors: klungsoyr k. Ann Neurol. 2023 Mar;93(3):551-562. doi: 10.1002/ana.26561. Epub 2022 Dec 12. Ann Neurol. 2023. PMID: 36433783
Anxiety, mood, and substance use disorders in adult men and women with and without attention-deficit/hyperactivity disorder: A substantive and methodological overview.
Hartman CA, Larsson H, Vos M, Bellato A, Libutzki B, Solberg BS, Chen Q, Du Rietz E, Mostert JC, Kittel-Schneider S, Cormand B, Ribasés M, Klungsøyr K, Haavik J, Dalsgaard S, Cortese S, Faraone SV, Reif A. Hartman CA, et al. Among authors: klungsoyr k. Neurosci Biobehav Rev. 2023 Aug;151:105209. doi: 10.1016/j.neubiorev.2023.105209. Epub 2023 May 5. Neurosci Biobehav Rev. 2023. PMID: 37149075 Free article. Review.
Severe Congenital Heart Defects and Cerebral Palsy.
Garne E, Goldsmith S, Barisic I, Braz P, Dakovic I, Gibson C, Hansen M, Hoei-Hansen CE, Hollung SJ, Klungsøyr K, Smithers-Sheedy H, Virella D, Badawi N, Watson L, McIntyre S. Garne E, et al. Among authors: klungsoyr k. J Pediatr. 2023 Nov;262:113617. doi: 10.1016/j.jpeds.2023.113617. Epub 2023 Jul 18. J Pediatr. 2023. PMID: 37473991 Free article.
Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007.
Boyle B, McConkey R, Garne E, Loane M, Addor MC, Bakker MK, Boyd PA, Gatt M, Greenlees R, Haeusler M, Klungsøyr K, Latos-Bielenska A, Lelong N, McDonnell R, Métneki J, Mullaney C, Nelen V, O'Mahony M, Pierini A, Rankin J, Rissmann A, Tucker D, Wellesley D, Dolk H. Boyle B, et al. Among authors: klungsoyr k. BJOG. 2013 May;120(6):707-16. doi: 10.1111/1471-0528.12146. Epub 2013 Feb 6. BJOG. 2013. PMID: 23384325
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe.
Barisic I, Odak L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Arriola L, Bergman J, Bianca S, Doray B, Khoshnood B, Klungsoyr K, McDonnell B, Pierini A, Rankin J, Rissmann A, Rounding C, Queisser-Luft A, Scarano G, Tucker D. Barisic I, et al. Among authors: klungsoyr k. Eur J Hum Genet. 2014 Aug;22(8):1026-33. doi: 10.1038/ejhg.2013.287. Epub 2014 Jan 8. Eur J Hum Genet. 2014. PMID: 24398798 Free PMC article.
Epidemiology of multiple congenital anomalies in Europe: a EUROCAT population-based registry study.
Calzolari E, Barisic I, Loane M, Morris J, Wellesley D, Dolk H, Addor MC, Arriola L, Bianchi F, Neville AJ, Budd JL, Klungsoyr K, Khoshnood B, McDonnell B, Nelen V, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Tucker D, Verellen-Dumoulin C, de Walle H, Garne E. Calzolari E, et al. Among authors: klungsoyr k. Birth Defects Res A Clin Mol Teratol. 2014 Apr;100(4):270-6. doi: 10.1002/bdra.23240. Epub 2014 Apr 11. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24723551
Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe.
Barisic I, Boban L, Loane M, Garne E, Wellesley D, Calzolari E, Dolk H, Addor MC, Bergman JE, Braz P, Draper ES, Haeusler M, Khoshnood B, Klungsoyr K, Pierini A, Queisser-Luft A, Rankin J, Rissmann A, Verellen-Dumoulin C. Barisic I, et al. Among authors: klungsoyr k. Eur J Hum Genet. 2015 Jun;23(6):746-52. doi: 10.1038/ejhg.2014.174. Epub 2014 Sep 3. Eur J Hum Genet. 2015. PMID: 25182137 Free PMC article.
187 results