| (AHP AWARD) DIFFERENTIATING BETWEEN CHILDREN WITH AND WITHOUT FRACTURE: DXA VERSUS PQCT N Crabtree, W Hogler, N Shaw OSTEOPOROSIS INTERNATIONAL 21, S457-S457, 2010 | | 2010 |
| 100 years of inherited metabolic disorders in Austria—A national registry of minimal birth prevalence, diagnosis, and clinical outcome of inborn errors of metabolism in … G Ramoser, F Caferri, B Radlinger, M Brunner‐Krainz, S Herbst, ... Journal of Inherited Metabolic Disease 45 (2), 144-156, 2022 | 12 | 2022 |
| 201 Bone safety data in adolescents with moderate-to-severe atopic dermatitis treated with abrocitinib: interim results from the JADE EXTEND MRI substudy J Zdybski, A Wollenberg, C Flohr, PM Brunner, W Högler, A Egeberg, ... Journal of Investigative Dermatology 143 (11), S366, 2023 | | 2023 |
| 764 Ethnic and seasonal variation in bloodspot vitamin D at birth J Large, S Uday, S Naseem, R Denmeade, P Goddard, MA Preece, ... Archives of Disease in Childhood 106 (Suppl 1), A106-A106, 2021 | | 2021 |
| 7th International Conference on Children's Bone Health ML Bianchi, N Bishop, W Högler, CB Langman, C Netelenbos | | |
| A comparison of bone geometry and cortical density at the mid-femur between prepuberty and young adulthood using magnetic resonance imaging W Högler, CJR Blimkie, CT Cowell, AF Kemp, J Briody, P Wiebe, ... Bone 33 (5), 771-778, 2003 | 90 | 2003 |
| A contemporary view of the definition and diagnosis of osteoporosis in children and adolescents LM Ward, DR Weber, CF Munns, W Högler, BS Zemel The Journal of Clinical Endocrinology & Metabolism 105 (5), e2088-e2097, 2020 | 102 | 2020 |
| A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism N Reisch, W Högler, S Parajes, IT Rose, V Dhir, J Götzinger, W Arlt, ... The Journal of Clinical Endocrinology & Metabolism 98 (10), E1620-E1625, 2013 | 81 | 2013 |
| A diagnostic algorithm for children with low alkaline phosphatase activities: lessons learned from laboratory screening for hypophosphatasia V Saraff, VK Narayanan, AJ Lawson, NJ Shaw, MA Preece, W Högler The Journal of pediatrics 172, 181-186. e1, 2016 | 50 | 2016 |
| A Diagnostic Algorithm for Children with Low Alkaline Phosphatase Activities: Lessons Learned from Laboratory Screening for Hypophosphatasia W Högler | | 2016 |
| A European Survey to Identify New Roads for Care, Training and Research Around Rare Metabolic Bone Diseases I Fernandez, SF Ahmed, N Bishop, ML Brandi, A Doulgeraki, G Haeusler, ... HORMONE RESEARCH IN PAEDIATRICS 86, 169-169, 2016 | | 2016 |
| A longitudinal, prospective, long-term registry of patients with hypophosphatasia P Kishnani, C Langman, A Linglart, E Mornet, K Ozono, ... Bone Abstracts 4, 2015 | 2 | 2015 |
| A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta A El-Gazzar, JA Mayr, B Voraberger, K Brugger, S Blouin, K Tischlinger, ... Bone Reports 15, 101110, 2021 | 5 | 2021 |
| A randomized, open-label Phase 2 study of KRN23, an investigational fully human Anti-FGF23 monoclonal antibody, in children with X-linked Hypophosphatemia (XLH) W Hogler, A Portale, E Imel, A Boot, A Linglart, R Padidela, M Whyte, ... Bone Abstracts 6, 2017 | | 2017 |
| A RANDOMIZED, OPEN-LABEL PHASE 2 STUDY OF KRN23, AN INVESTIGATIONAL FULLY HUMAN ANTIFGF-23 MONOCLONAL ANTIBODY, IN CHILDREN WITH X-LINKED HYPOPHOSPHATEMIA (XLH): 64-WEEKS RESULTS T Carpenter, E Imel, A Boot, W Hogler, A Linglart, R Padidela, W van't Hoff, ... OSTEOPOROSIS INTERNATIONAL 28, S63-S63, 2017 | | 2017 |
| A rare cause of rickets S Sakka, S Uday, T Randell, JH Davies, VB Arya, C Brain, J Allgrove, ... Bone Abstracts 6, 2017 | 1 | 2017 |
| A roadmap to gene discoveries and novel therapies in monogenic low and high bone mass disorders MM Formosa, DJM Bergen, CL Gregson, A Maurizi, A Kämpe, ... Frontiers in Endocrinology 12, 709711, 2021 | 18 | 2021 |
| A three-year longitudinal study comparing bone mass, density, and geometry measured by DXA, pQCT, and bone turnover markers in children with PKU taking L-amino acid or … A Daly, W Högler, N Crabtree, N Shaw, S Evans, A Pinto, R Jackson, ... Nutrients 13 (6), 2075, 2021 | 12 | 2021 |
| Abrupt onset of severe passenger lymphocyte syndrome after allogeneic bone marrow transpantation (BMT) in a 7-year-old boy. W Hoegler, G Kropshofer, D Nachbaur, G Wehl, A Heitger, W Mayer, ... BLOOD 96 (11), 355B-355B, 2000 | | 2000 |
| Abrupt onset of severe passenger lymphocyte syndrome after HLA‐mismatched unrelated bone marrow transplantation in a seven‐year‐old boy W Hoegler, D Nachbaur, G Kropshofer, G Wehl, D Schoenitzer, ... Medical and pediatric oncology 38 (2), 143-144, 2002 | 6 | 2002 |
