Items where authors include "Högler, W."

Article

Hofmann, C.E., Harmatz, P., Vockley, J. et al. (8 more authors) (2019) Efficacy and safety of asfotase alfa in infants and young children with hypophosphatasia : a phase 2 open-label study. The Journal of Clinical Endocrinology & Metabolism, 104 (7). pp. 2735-2747. ISSN 0021-972X

Idkowiak, J., Elhassan, Y.S., Mannion, P. et al. (13 more authors) (2019) Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children. European Journal of Endocrinology, 180 (3). pp. 213-221. ISSN 0804-4643

Högler, W., Scott, J., Bishop, N. orcid.org/0000-0001-7263-8546 et al. (6 more authors) (2017) The effect of whole body vibration training on bone and muscle function in children with osteogenesis imperfecta. Journal of Clinical Endocrinology & Metabolism, 102 (8). pp. 2734-2743. ISSN 0021-972X

Webb, E.A., Balasubramanian, M., Fratzl-Zelman, N. et al. (16 more authors) (2017) Phenotypic spectrum in osteogenesis imperfecta due to mutations in TMEM38B: unravelling a complex cellular defect. Journal of Clinical Endocrinology and Metabolism, 102 (6). pp. 2019-2028. ISSN 0021-972X

Crabtree, N.J., Shaw, N.J., Bishop, N.J. orcid.org/0000-0001-7263-8546 et al. (10 more authors) (2017) Amalgamated Reference Data for Size-Adjusted Bone Densitometry Measurements in 3598 Children and Young Adults - The Alphabet Study. Journal of Bone and Mineral Research, 32 (1). pp. 172-180. ISSN 1523-4681

Pollitt, R.C. orcid.org/0000-0002-8864-397X, Saraff, V., Dalton, A. et al. (10 more authors) (2016) Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations. American Journal of Medical Genetics Part A. ISSN 1552-4825

Dhillon, N., Karthikeyan, A., Castle, A. et al. (6 more authors) (2016) Natural history of retinopathy in children and young people with type 1 diabetes. Eye, 30 (7). pp. 987-991. ISSN 0950-222X