Showing 1 - 20 results of 31 for search 'Wolfgang Högler', query time: 0.06s
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Mechanisms of Bone Fragility: From Osteogenesis Imperfecta to Secondary Osteoporosis by Ahmed El-Gazzar, Wolfgang Högler
Published 2021-01-01
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Rickets and osteomalacia: a call for action to protect immigrants and ethnic risk groups by Wolfgang Högler, Craig F Munns
Published 2016-04-01
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Influence of maternal socioeconomic deprivation and living environment on newborn bloodspot 25-hydroxyvitamin D levels by Wolfgang Högler, Wolfgang Högler, Katharina Tischlinger, William D. Fraser, William D. Fraser, Jonathan C. Y. Tang, Jonathan C. Y. Tang, Suma Uday, Suma Uday
Published 2022-11-01
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Association of bone mineralization markers with dietary nutrient intake in adolescents with and without biochemical osteomalacia by Nasser M. Al-Daghri, Shaun Sabico, Kaiser Wani, Syed Danish Hussain, Sobhy Yakout, Naji Aljohani, Naji Aljohani, Suma Uday, Suma Uday, Wolfgang Högler, Wolfgang Högler
Published 2023-07-01
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Spontaneous reshaping of vertebral fractures in an adolescent with osteogenesis imperfecta by Rodrigo Montero-Lopez, Elisabeth Laurer, Katharina Tischlinger, Dóra Nagy, Mario Scala, Wolfgang Kranewitter, Gerald Webersinke, Thomas Hörtenhuber, Wolfgang Högler
Published 2022-06-01
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Diagnostic delay is common among patients with hypophosphatasia: initial findings from a longitudinal, prospective, global registry by Wolfgang Högler, Craig Langman, Hugo Gomes da Silva, Shona Fang, Agnès Linglart, Keiichi Ozono, Anna Petryk, Cheryl Rockman-Greenberg, Lothar Seefried, Priya S. Kishnani
Published 2019-02-01
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P494: An analysis of ALPL gene variants in patients with hypophosphatasia from the Global Hypophosphatasia Registry by Priya Kishnani, Kathryn Dahir, Gabriel Martos-Moreno, Agnès Linglart, Anna Petryk, William Mowrey, Shona Fang, Cheryl Rockman-Greenberg, Keiichi Ozono, Wolfgang Högler, Lothar Seefried
Published 2023-01-01
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Clinical profiles of treated and untreated adults with hypophosphatasia in the Global HPP Registry by Kathryn M. Dahir, Lothar Seefried, Priya S. Kishnani, Anna Petryk, Wolfgang Högler, Agnès Linglart, Gabriel Ángel Martos-Moreno, Keiichi Ozono, Shona Fang, Cheryl Rockman-Greenberg
Published 2022-07-01
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A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta by Ahmed El-Gazzar, Johannes A. Mayr, Barbara Voraberger, Karin Brugger, Stéphane Blouin, Katharina Tischlinger, Hans-Christoph Duba, Holger Prokisch, Nadja Fratzl-Zelman, Wolfgang Högler
Published 2021-12-01
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Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry by Priya S. Kishnani, Gabriel Ángel Martos-Moreno, Agnès Linglart, Anna Petryk, Andrew Messali, Shona Fang, Cheryl Rockman-Greenberg, Keiichi Ozono, Wolfgang Högler, Lothar Seefried, Kathryn M. Dahir
Published 2024-03-01
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The Growth Hormone Deficiency (GHD) Reversal Trial: effect on final height of discontinuation versus continuation of growth hormone treatment in pubertal children with isolated GHD... by Elizabeth Brettell, Wolfgang Högler, Rebecca Woolley, Carole Cummins, Jonathan Mathers, Raymond Oppong, Laura Roy, Adam Khan, Charmaine Hunt, Mehul Dattani, on behalf of the G. H. D. study group
Published 2023-08-01
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Growth and Body Composition in PKU Children—A Three-Year Prospective Study Comparing the Effects of L-Amino Acid to Glycomacropeptide Protein Substitutes by Anne Daly, Wolfgang Högler, Nicola Crabtree, Nick Shaw, Sharon Evans, Alex Pinto, Richard Jackson, Boyd J. Strauss, Gisela Wilcox, Júlio C. Rocha, Catherine Ashmore, Anita MacDonald
Published 2021-04-01
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A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders by Melissa M. Formosa, Melissa M. Formosa, Dylan J. M. Bergen, Dylan J. M. Bergen, Celia L. Gregson, Antonio Maurizi, Anders Kämpe, Anders Kämpe, Natalia Garcia-Giralt, Wei Zhou, Daniel Grinberg, Diana Ovejero Crespo, M. Carola Zillikens, Graham R. Williams, J. H. Duncan Bassett, Maria Luisa Brandi, Luca Sangiorgi, Susanna Balcells, Wolfgang Högler, Wolfgang Högler, Wim Van Hul, Outi Mäkitie, Outi Mäkitie, Outi Mäkitie
Published 2021-08-01
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Establishing the first pan-European Registry for rare bone and mineral disorders: EuRR-Bone by Corinna Grasemann, Marina Mordenti, Inês Alves, Rebecca Skarberg, Ondrej Soucek, Marco Roos, M. Kassim Javaid, S. Faisal Ahmed, Agnès Lignart, Klaus Mohnike, Wolfgang Högler, Luca Sangiorgi, Natasha M. Appelman-Dijkstra
Published 2020-10-01
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