Hasil Pencarian - Else Merckoll

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  1. 1
    Radiographic classifications in Perthes disease: Interobserver agreement and association with femoral head sphericity at 5-year follow-up

    Radiographic classifications in Perthes disease: Interobserver agreement and association with femoral head sphericity at 5-year follow-up oleh Stefan Huhnstock, Svein Svenningsen, Else Merckoll, Anthony Catterall, Terje Terjesen, Ola Wiig

    Diterbitkan 2017-09-01
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  2. 2
    A comparison of 3 different methods for assessment of skeletal age when treating leg-length discrepancies: an inter- and intra-observer study

    A comparison of 3 different methods for assessment of skeletal age when treating leg-length discrepancies: an inter- and intra-observer study oleh Anne Berg Breen, Harald Steen, Are Pripp, Ragnhild Gunderson, Hilde Kristine Sandberg Mentzoni, Else Merckoll, Wajeeha Zaidi, Mikael Lambert, Ivan Hvid, Joachim Horn

    Diterbitkan 2022-01-01
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  3. 3
    A monoallelic UXS1 variant associated with short‐limbed short stature

    A monoallelic UXS1 variant associated with short‐limbed short stature oleh Cecilie F. Rustad, Paul Hoff Backe, Chunsheng Jin, Else Merckoll, Kristian Tveten, Marissa Lucy Maciej‐Hulme, Niclas Karlsson, Trine Prescott, Elise Sandås Sand, Berit Woldseth, Katja Benedikte Prestø Elgstøen, Øystein L. Holla

    Diterbitkan 2024-06-01
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  4. 4
    Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13

    Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13 oleh Prince Jacob, Hillevi Lindelöf, Cecilie F. Rustad, Vernon Reid Sutton, Shahida Moosa, Prajna Udupa, Anna Hammarsjö, Gandham SriLakshmi Bhavani, Dominyka Batkovskyte, Kristian Tveten, Ashwin Dalal, Eva Horemuzova, Ann Nordgren, Emma Tham, Hitesh Shah, Else Merckoll, Laura Orellana, Gen Nishimura, Katta M. Girisha, Giedre Grigelioniene

    Diterbitkan 2023-11-01
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  5. 5
    Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations.

    Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations. oleh Zheng Wang, Aritoshi Iida, Noriko Miyake, Koji M Nishiguchi, Kosuke Fujita, Toru Nakazawa, Abdulrahman Alswaid, Mohammed A Albalwi, Ok-Hwa Kim, Tae-Joon Cho, Gye-Yeon Lim, Bertrand Isidor, Albert David, Cecilie F Rustad, Else Merckoll, Jostein Westvik, Eva-Lena Stattin, Giedre Grigelioniene, Ikuyo Kou, Masahiro Nakajima, Hirohumi Ohashi, Sarah Smithson, Naomichi Matsumoto, Gen Nishimura, Shiro Ikegawa

    Diterbitkan 2016-01-01
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