日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

XLH Matters: an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes

XLH Matters:一个不断发展的项目,旨在探讨最新进展并分享临床经验,以改善患者预后。

Seefried, Lothar; Aliberti, Ferdinando; Heier, Cathrine Alsaker; Arango-Sancho, Pedro; Biosse Duplan, Martin; Sakka, Sophia D; Emma, Francesco; Gardiner, Oliver; Javaid, Muhammad Kassim; Ferreira-Santos, Rui M; Raimann, Adalbert; Rak, Kristen; Bubbear, Judith S; Cheung, Moira S; Beck-Nielsen, Signe Sparre; Mindler, Gabriel T; Linglart, Agnès

XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemia

XLH Matters 2024:专家见解和实用工具,旨在改善X连锁低磷血症患者的护理

Seefried, Lothar; Alzahrani, Ali S; Wagner, Carsten A; Eade, Damian; Fintini, Danilo; Haffner, Dieter; Frookh Jamal, Hasan; Bubbear, Judith S; Guazzarotti, Laura; Cheung, Moira S; Abid, Noina; Costa-Reis, Patrícia; Ferreira Santos, Rui; Beck-Nielsen, Signe Sparre; Linglart, Agnès

EndoCompass Project: Research Roadmap for Calcium and Bone Endocrinology

EndoCompass项目:钙和骨内分泌学研究路线图

Jähn-Rickert, Katharina; Tomšić, Karin Zibar; Anastasilakis, Athanasios D; Bertocchio, Jean-Philippe; Brandi, Maria Luisa; Fassnacht, Martin; Cheung, Moira Shang-Mei; Gevers, Evelien; Gittoes, Neil; Mäkitie, Outi; Martos-Moreno, Gabriel Ángel; Milovanovic, Petar; Raimann, Adalbert; Tencerova, Michaela; Tsourdi, Elena; Vlug, Annegreet G; Högler, Wolfgang; Kamenický, Peter

Bone health in a U.K. cohort of youth living with perinatally acquired HIV-1: a longitudinal study

英国一组围产期感染 HIV-1 的青少年骨骼健康状况:一项纵向研究

Henderson, Merle; Blenkinsop, Alexandra; Ratmann, Oliver; Cheung, Moira; Lyall, Hermione; Fidler, Sarah; Foster, Caroline

Eiken syndrome with parathyroid hormone resistance due to a novel parathyroid hormone receptor type 1 mutation: clinical features and functional analysis.

因新型甲状旁腺激素受体 1 型突变引起的甲状旁腺激素抵抗的 Eiken 综合征:临床特征和功能分析

Calder Alistair D, Allgrove Jeremy, Höppner Jakob, Cheung Moira, Alexander Saji, Garagnani Lorenzo, Thakker Rajesh, Jüppner Harald, Gardella Thomas J, Holder-Espinasse Muriel

Higher rates of non-skeletal complications and greater healthcare needs in achondroplasia compared to the general UK population: a matched cohort study using the CPRD database

与英国普通人群相比,软骨发育不全患者的非骨骼并发症发生率更高,医疗保健需求更大:一项使用CPRD数据库的匹配队列研究

Pimenta, Jeanne M; Irving, Melita; Cheung, Moira; Mazzeo, Louise; Landis, Sarah; Mukherjee, Swati

Simultaneous Kidney and Parathyroid Transplantation in the Management of Genetic Hypoparathyroidism in a Child

儿童遗传性甲状旁腺功能减退症的同步肾脏和甲状旁腺移植

Vallant, Natalie; Sinha, Manish D; Cheung, Moira; Ware, Nick; Jones, Helen; Buck, Jackie; Boffa, Catherine; Irving, Melita; Carroll, Paul V; Hubbard, Johnathan; Gökmen, Refik; Rees, Lesley; Gogalniceanu, Petrut; Kessaris, Nicos

Patient-Reported Complications, Symptoms, and Experiences of Living With X-Linked Hypophosphatemia Across the Life-Course

患者自述的X连锁低磷血症终生并发症、症状和生活体验

Cheung, Moira; Rylands, Angela J; Williams, Angela; Bailey, Karen; Bubbear, Judith

Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era

放射基因组学时代罕见骨骼发育不良的诊断率

Sabir, Ataf H; Morley, Elizabeth; Sheikh, Jameela; Calder, Alistair D; Beleza-Meireles, Ana; Cheung, Moira S; Cocca, Alessandra; Jansson, Mattias; Lillis, Suzanne; Patel, Yogen; Yau, Shu; Hall, Christine M; Offiah, Amaka C; Irving, Melita

Clinical guidelines for burosumab in the treatment of XLH in children and adolescents: British paediatric and adolescent bone group recommendations

布罗索单抗治疗儿童和青少年X连锁低钙尿症的临床指南:英国儿科和青少年骨骼组的建议

Padidela, Raja; Cheung, Moira S; Saraff, Vrinda; Dharmaraj, Poonam