Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jorieke Bergman"'
Autor:
Nafise Ghalandari, Ineke Crijns, Jorieke Bergman, Radboud Dolhain, Eugène van Puijenbroek, Mieke Hazes
Aim To evaluate the number and nature of reported congenital malformations (CMs) after intrauterine exposure to non-tumour necrosis factor inhibitors (non-TNFis) compared to certolizumab pegol (CZP) Material and methods A retrospective comparative st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53106dcdb403472f7051b5bf94c437ab
https://doi.org/10.22541/au.165174666.67592213/v1
https://doi.org/10.22541/au.165174666.67592213/v1
Autor:
Aizati Daud, Bergsma, Eefke, Jorieke Bergman, Walle, Hermien De, Kerstjens-Frederikse, Wilhelmina, Bijker, Bert, Hak, Eelko, Wilffert, Bob
Questionnaire used in the survey (translated in English). Table S1: The likelihood of having a good attitude towards pharmacogenetics testing given respondent characteristics (PDF 510 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::826560dbc7b49bad9652c32e2e057273
Autor:
Kate E, Best, Marie-Claude, Addor, Larraitz, Arriola, Eszter, Balku, Ingeborg, Barisic, Fabrizio, Bianchi, Elisa, Calzolari, Rhonda, Curran, Berenice, Doray, Elizabeth, Draper, Ester, Garne, Miriam, Gatt, Martin, Haeusler, Jorieke, Bergman, Babak, Khoshnood, Kari, Klungsoyr, Carmen, Martos, Anna, Materna-Kiryluk, Carlos, Matias Dias, Bob, McDonnell, Carmel, Mullaney, Vera, Nelen, Mary, O'Mahony, Annette, Queisser-Luft, Hanitra, Randrianaivo, Anke, Rissmann, Catherine, Rounding, Antonin, Sipek, Rosie, Thompson, David, Tucker, Diana, Wellesley, Natalya, Zymak-Zakutnia, Judith, Rankin
Publikováno v:
Birth Defects Research. Part A: Clinical and Molecular Teratology, 100(9), 695-702. Wiley-Blackwell
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Best, K E, Addor, M-C, Arriola, L, Balku, E, Barisic, I, Bianchi, F, Calzolari, E, Curran, R, Doray, B, Draper, E, Garne, E, Gatt, M, Haeusler, M, Bergman, J, Khoshnood, B, Klungsoyr, K, Martos, C, Materna-Kiryluk, A, Matias Dias, C, McDonnell, B, Mullaney, C, Nelen, V, O'Mahony, M, Queisser-Luft, A, Randrianaivo, H, Rissmann, A, Rounding, C, Sipek, A, Thompson, R, Tucker, D, Wellesley, D, Zymak-Zakutnia, N & Rankin, J 2014, ' Hirschsprung's disease prevalence in Europe. A register based study ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 100, no. 9, pp. 695-702 . https://doi.org/10.1002/bdra.23269
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Best, K E, Addor, M-C, Arriola, L, Balku, E, Barisic, I, Bianchi, F, Calzolari, E, Curran, R, Doray, B, Draper, E, Garne, E, Gatt, M, Haeusler, M, Bergman, J, Khoshnood, B, Klungsoyr, K, Martos, C, Materna-Kiryluk, A, Matias Dias, C, McDonnell, B, Mullaney, C, Nelen, V, O'Mahony, M, Queisser-Luft, A, Randrianaivo, H, Rissmann, A, Rounding, C, Sipek, A, Thompson, R, Tucker, D, Wellesley, D, Zymak-Zakutnia, N & Rankin, J 2014, ' Hirschsprung's disease prevalence in Europe. A register based study ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 100, no. 9, pp. 695-702 . https://doi.org/10.1002/bdra.23269
Background: Hirschsprung's disease is a congenital gut motility disorder, characterised by the absence of the enteric ganglion cells along the distal gut. The aim of this study was to describe the epidemiology of Hirschsprung's disease, including add
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::03186882704b91eecd9a2db5c8f6f605
https://research.rug.nl/en/publications/71d00052-685d-4fe7-bd7b-0d4a60cc9a9d
https://research.rug.nl/en/publications/71d00052-685d-4fe7-bd7b-0d4a60cc9a9d
Publikováno v:
Pharmacoepidemiology & Drug Safety; Sep2022 Supplement S1, Vol. 31, p3-628, 626p
Publikováno v:
Annals of the Rheumatic Diseases; 2022 Supplement, Vol. 81, p1-211, 211p
Autor:
Daud, Aizati N. A.1,2 n.a.a.daud@rug.nl, Bergsma, Eefke L.1, Bergman, Jorieke E. H.3, De Walle, Hermien E. K.3, Kerstjens-Frederikse, Wilhelmina S.3, Bijker, Bert J.1, Hak, Eelko1, Wilffert, Bob1,4
Publikováno v:
BMC Pregnancy & Childbirth. 4/14/2017, Vol. 17, p1-9. 9p.
Autor:
Thurin, Nicolas H., Pajouheshnia, Romin, Roberto, Giuseppe, Dodd, Caitlin, Hyeraci, Giulia, Bartolini, Claudia, Paoletti, Olga, Nordeng, Hedvig, Wallach‐Kildemoes, Helle, Ehrenstein, Vera, Dudukina, Elena, MacDonald, Thomas, De Paoli, Giorgia, Loane, Maria, Damase‐Michel, Christine, Beau, Anna‐Belle, Droz‐Perroteau, Cécile, Lassalle, Régis, Bergman, Jorieke, Swart, Karin
Publikováno v:
Clinical Pharmacology & Therapeutics; Jan2022, Vol. 111 Issue 1, p321-331, 11p
Autor:
Barisic, Ingeborg1 ingeborg.barisic@kdb.hr, Boban, Ljubica1 ljubica.boban7@gmail.com, Greenlees, Ruth2 R.Greenlees@ulster.ac.uk, Garne, Ester3 ester.garne@rsyd.dk, Wellesley, Diana4 dgw@soton.ac.uk, Calzolari, Elisa5 nvm@unife.it, Addor, Marie-Claude6 marie-claude.addor@chuv.ch, Arriola, Larraitz7 l-arriola@ej-gv.es, Bergman, Jorieke E. H.8 j.e.h.van.kammen@umcg.nl, Braz, Paula9 carlos.dias@insa.min-saude.pt, Budd, Judith L. S.10 jlsb1@leicester.ac.uk, Gatt, Miriam11 miriam.gatt@gov.mt, Haeusler, Martin12 martin.haeusler@medunigraz.at, Khoshnood, Babak13 babak.khoshnood@inserm.fr, Klungsoyr, Kari14 kari.klungsoyr@fhi.no, McDonnell, Bob15 bob.mcdonnell@hse.ie, Nelen, Vera16 vera.nelen@pih.provant.be, Pierini, Anna17 apier@ifc.cnr.it, Queisser-Wahrendorf, Annette18 queisser@kinder.klinik.uni-mainz.de, Rankin, Judith19 judith.rankin@ncl.ac.uk
Publikováno v:
Orphanet Journal of Rare Diseases. 2014, Vol. 9 Issue 1, p1-19. 19p.
Autor:
Springett, Anna, Wellesley, Diana, Greenlees, Ruth, Loane, Maria, Addor, Marie‐Claude, Arriola, Larraitz, Bergman, Jorieke, Cavero‐Carbonell, Clara, Csaky‐Szunyogh, Melinda, Draper, Elizabeth S., Garne, Ester, Gatt, Miriam, Haeusler, Martin, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, Dias, Carlos Matias, McDonnell, Robert, Nelen, Vera, O'Mahony, Mary
Publikováno v:
American Journal of Medical Genetics. Part A; Dec2015, Vol. 167A Issue 12, p3062-3069, 8p
Publikováno v:
Annals of the Rheumatic Diseases. 81:83.2-83
BackgroundTumor necrosis factor-α inhibitors (TNFis) such as certolizumab pegol (CZP), are a subgroup of biologics, which have shown no increase in risk of congenital malformations (CMs) after use during pregnancy. (1) However, for the subgroup of n