Works matching AU Haeusler, Martin


Results: 99
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    Epidemiology of Pierre‐Robin sequence in Europe: A population‐based EUROCAT study.

    Published in:
    Paediatric & Perinatal Epidemiology, 2021, v. 35, n. 5, p. 530, doi. 10.1111/ppe.12776
    By:
    • Santoro, Michele;
    • Coi, Alessio;
    • Barišić, Ingeborg;
    • Pierini, Anna;
    • Addor, Marie‐Claude;
    • Baldacci, Silvia;
    • Ballardini, Elisa;
    • Boban, Ljubica;
    • Braz, Paula;
    • Cavero‐Carbonell, Clara;
    • de Walle, Hermien E. K.;
    • Draper, Elizabeth S.;
    • Gatt, Miriam;
    • Haeusler, Martin;
    • Klungsøyr, Kari;
    • Kurinczuk, Jennifer J.;
    • Materna‐Kiryluk, Anna;
    • Lanzoni, Monica;
    • Lelong, Nathalie;
    • Luyt, Karen
    Publication type:
    Article
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    Multilevel analyses of related public health indicators: The European Surveillance of Congenital Anomalies (EUROCAT) Public Health Indicators.

    Published in:
    2020
    By:
    • Best, Kate E.;
    • Rankin, Judith;
    • Dolk, Helen;
    • Loane, Maria;
    • Haeusler, Martin;
    • Nelen, Vera;
    • Verellen‐Dumoulin, Christine;
    • Garne, Ester;
    • Sayers, Gerardine;
    • Mullaney, Carmel;
    • O'Mahony, Mary T.;
    • Gatt, Miriam;
    • De Walle, Hermien;
    • Klungsoyr, Kari;
    • Carolla, Olatz Mokoroa;
    • Cavero‐Carbonell, Clara;
    • Kurinczuk, Jennifer J.;
    • Draper, Elizabeth S.;
    • Tucker, David;
    • Wellesley, Diana
    Publication type:
    journal article
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    Molecular pathophysiology of human MICU1 deficiency.

    Published in:
    Neuropathology & Applied Neurobiology, 2021, v. 47, n. 6, p. 840, doi. 10.1111/nan.12694
    By:
    • Kohlschmidt, Nicolai;
    • Elbracht, Miriam;
    • Czech, Artur;
    • Häusler, Martin;
    • Phan, Vietxuan;
    • Töpf, Ana;
    • Huang, Kai‐Ting;
    • Bartok, Adam;
    • Eggermann, Katja;
    • Zippel, Stephanie;
    • Eggermann, Thomas;
    • Freier, Erik;
    • Groß, Claudia;
    • Lochmüller, Hanns;
    • Horvath, Rita;
    • Hajnóczky, György;
    • Weis, Joachim;
    • Roos, Andreas
    Publication type:
    Article
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    Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients.

    Published in:
    2020
    By:
    • Jarius, Sven;
    • Lechner, Christian;
    • Wendel, Eva M.;
    • Baumann, Matthias;
    • Breu, Markus;
    • Schimmel, Mareike;
    • Karenfort, Michael;
    • Marina, Adela Della;
    • Merkenschlager, Andreas;
    • Thiels, Charlotte;
    • Blaschek, Astrid;
    • Salandin, Michela;
    • Leiz, Steffen;
    • Leypoldt, Frank;
    • Pschibul, Alexander;
    • Hackenberg, Annette;
    • Hahn, Andreas;
    • Syrbe, Steffen;
    • Strautmanis, Jurgis;
    • Häusler, Martin
    Publication type:
    journal article
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    Amniotic band syndrome and limb body wall complex in Europe 1980–2019.

    Published in:
    American Journal of Medical Genetics. Part A, 2023, v. 191, n. 4, p. 995, doi. 10.1002/ajmg.a.63107
    By:
    • Bergman, Jorieke E. H.;
    • Barišić, Ingeborg;
    • Addor, Marie‐Claude;
    • Braz, Paula;
    • Cavero‐Carbonell, Clara;
    • Draper, Elizabeth S.;
    • Echevarría‐González‐de‐Garibay, Luis J.;
    • Gatt, Miriam;
    • Haeusler, Martin;
    • Khoshnood, Babak;
    • Klungsøyr, Kari;
    • Kurinczuk, Jennifer J.;
    • Latos‐Bielenska, Anna;
    • Luyt, Karen;
    • Martin, Danielle;
    • Mullaney, Carmel;
    • Nelen, Vera;
    • Neville, Amanda J.;
    • O'Mahony, Mary T.;
    • Perthus, Isabelle
    Publication type:
    Article
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    Epidemiology of achondroplasia: A population‐based study in Europe.

    Published in:
    American Journal of Medical Genetics. Part A, 2019, v. 179, n. 9, p. 1791, doi. 10.1002/ajmg.a.61289
    By:
    • Coi, Alessio;
    • Santoro, Michele;
    • Garne, Ester;
    • Pierini, Anna;
    • Addor, Marie‐Claude;
    • Alessandri, Jean‐Luc;
    • Bergman, Jorieke E. H.;
    • Bianchi, Fabrizio;
    • Boban, Ljubica;
    • Braz, Paula;
    • Cavero‐Carbonell, Clara;
    • Gatt, Miriam;
    • Haeusler, Martin;
    • Klungsøyr, Kari;
    • Kurinczuk, Jennifer J.;
    • Lanzoni, Monica;
    • Lelong, Nathalie;
    • Luyt, Karen;
    • Mokoroa, Olatz;
    • Mullaney, Carmel
    Publication type:
    Article
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    Congenital Anomalies Associated with Trisomy 18 or Trisomy 13: A Registry-Based Study in 16 European Countries, 2000-2011.

    Published in:
    American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3062, doi. 10.1002/ajmg.a.37355
    By:
    • 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
    Publication type:
    Article
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    Fraser Syndrome: Epidemiological Study in a European Population.

    Published in:
    American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 5, p. 1012, doi. 10.1002/ajmg.a.35839
    By:
    • Barisic, Ingeborg;
    • Odak, Ljubica;
    • Loane, Maria;
    • Garne, Ester;
    • Wellesley, Diana;
    • Calzolari, Elisa;
    • Dolk, Helen;
    • Addor, Marie‐Claude;
    • Arriola, Larraitz;
    • Bergman, Jorieke;
    • Bianca, Sebastiano;
    • Boyd, Patricia A.;
    • Draper, Elizabeth S;
    • Gatt, Miriam;
    • Haeusler, Martin;
    • Khoshnood, Babak;
    • Latos‐Bielenska, Anna;
    • McDonnell, Bob;
    • Pierini, Anna;
    • Rankin, Judith
    Publication type:
    Article
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    Oligoclonal bands predict multiple sclerosis in children with optic neuritis.

    Published in:
    Annals of Neurology, 2015, v. 77, n. 6, p. 1076, doi. 10.1002/ana.24409
    By:
    • Heussinger, Nicole;
    • Kontopantelis, Evangelos;
    • Gburek‐Augustat, Janina;
    • Jenke, Andreas;
    • Vollrath, Gesa;
    • Korinthenberg, Rudolf;
    • Hofstetter, Peter;
    • Meyer, Sascha;
    • Brecht, Isabel;
    • Kornek, Barbara;
    • Herkenrath, Peter;
    • Schimmel, Mareike;
    • Wenner, Kirsten;
    • Häusler, Martin;
    • Lutz, Soeren;
    • Karenfort, Michael;
    • Blaschek, Astrid;
    • Smitka, Martin;
    • Karch, Stephanie;
    • Piepkorn, Martin
    Publication type:
    Article
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    Holt Oram syndrome: a registry-based study in Europe.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/s13023-014-0156-y
    By:
    • Barisic, Ingeborg;
    • Boban, Ljubica;
    • Greenlees, Ruth;
    • Garne, Ester;
    • Wellesley, Diana;
    • Calzolari, Elisa;
    • Addor, Marie-Claude;
    • Arriola, Larraitz;
    • Bergman, Jorieke E. H.;
    • Braz, Paula;
    • Budd, Judith L. S.;
    • Gatt, Miriam;
    • Haeusler, Martin;
    • Khoshnood, Babak;
    • Klungsoyr, Kari;
    • McDonnell, Bob;
    • Nelen, Vera;
    • Pierini, Anna;
    • Queisser-Wahrendorf, Annette;
    • Rankin, Judith
    Publication type:
    Article
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    Can glucose tolerance test predict fetal hyperinsulinism?

    Published in:
    BJOG: An International Journal of Obstetrics & Gynaecology, 2000, v. 107, n. 12, p. 1480, doi. 10.1111/j.1471-0528.2000.tb11671.x
    By:
    • Weiss, Peter A. M.;
    • Haeusler, Martin;
    • Tamussino, Karl;
    • Haas, Josef
    Publication type:
    Article
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