Use of burosumab in McCune Albright syndrome: case report and review of literature in mosaic disorders with FGF23 overproduction., PMID:40491596
                                            Burosumab treatment of tumour-induced osteomalacia from a rib lesion., PMID:40379296
                                            Real-world efficacy and safety of burosumab in tumor-induced osteomalacia: case series from an early access program., PMID:40329993
                                            Predictors of response to burosumab in adults with X-linked hypophosphatemia: real-world data from an Italian cohort., PMID:40323576
                                            Real-World Effectiveness of Burosumab Versus Oral Phosphate and Active Vitamin D in Adults With X-Linked Hypophosphatemia., PMID:40314226
                                            Burosumab treatment of a child with McCune-Albright syndrome/polyostotic fibrous dysplasia: challenges and benefits., PMID:40297189
                                            A Child with Cutaneous-Skeletal Hypophosphatemia Syndrome Caused by a Mosaic HRAS Mutation: Outcome of Treatment with Anti-FGF23 Antibody., PMID:40295341
                                            Advancing patient evidence in XLH (APEX): rationale and design of a real-world XLH global data unification program., PMID:40260280
                                            Fibroblast growth factor 23 neutralizing antibody partially rescues bone loss and increases hematocrit in sickle cell disease mice., PMID:40155665
                                            Two Cases of Tumor-induced Osteomalacia Resulting in Surgical Resection During Burosumab Therapy., PMID:40058863
                                            Molecular pathophysiology of chronic kidney disease-mineral and bone disorder: Focus on the fibroblast growth factor 23-Klotho axis and bone turnover dynamics., PMID:40014035
                                            X-Linked Hypophosphataemia and Burosumab: A Systemic Disease With a New Treatment., PMID:40012305
                                            [Rare osteological diseases in the rheumatological consultation: hypophosphatasia and phosphate loss syndromes]., PMID:39982479
                                            Burosumab Treatment in a Girl With Cutaneous Skeletal Hypophosphatemia Syndrome: 2-Year Follow-Up., PMID:39925163
                                            Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia., PMID:39814982
                                            Treatment Advances in Tumor-Induced Osteomalacia., PMID:39755803
                                            Nephrocalcinosis tendency does not worsen under burosumab treatment for X-linked hypophosphatemic rickets: a multicenter pediatric study., PMID:39687707
                                            Protease-activated receptor 2 deficient mice develop less angiotensin II induced left ventricular hypertrophy but more cardiac fibrosis., PMID:39637045
                                            Long-term control by immune checkpoint inhibitors in a lung cancer patient with chronic kidney disease., PMID:39516036
                                            Analytical interference of Burosumab therapy on intact fibroblast growth factor 23 (iFGF23) measurements using an immunoassay: preliminary evaluation., PMID:39494895
                                            Effective bone healing after corrective osteotomy in a patient with FGF23-related hypophosphatemic disease using short-term burosumab treatment., PMID:39375070
                                            Pharmacodynamic Exposure-Response Analysis of Fracture Count Data Following Treatment with Burosumab in Patients with XLH., PMID:39344278
                                            Improvement of Fibrous Dysplasia After Burosumab Therapy in a Pediatric Patient with McCune-Albright Syndrome: A Case Report., PMID:39303050
                                            X-linked hypophosphatemic rickets and nephrocalcinosis: clinical characteristics of a single-center pediatric cohort in North America before and after burosumab., PMID:39156019
                                            NFATc1 Is Required for Vitamin D- and Phosphate-Mediated Regulation of Osteocyte Lacuno-Canalicular Remodeling., PMID:39024412
                                            Burosumab treatment of X-linked hypophosphatemia patients: interim analysis of the SUNFLOWER longitudinal, observational cohort study., PMID:39015507
                                            Sclerostin inhibition in rare bone diseases: Molecular understanding and therapeutic perspectives., PMID:39007037
                                            Molecular Interaction of Soluble Klotho with FGF23 in the Pathobiology of Aortic Valve Lesions Induced by Chronic Kidney Disease., PMID:38993571
                                            Multiarray screening identifies plasma proteins associated with Th17 cell differentiation and viral defense in coincident asthma and obesity., PMID:38967090
                                            Safety and efficacy of burosumab in improving phosphate metabolism, bone health, and quality of life in adolescents with X-linked hypophosphatemic rickets., PMID:38950880
                                            Improved Oral Health in Adults With X-Linked Hypophosphatemia Treated With Burosumab., PMID:38864457
                                            Cardiovascular health in pediatric patients with X-linked hypophosphatemia under two years of burosumab therapy., PMID:38818505
                                            Interplay of clinical biomarkers in allergic asthma diagnosis and severity: A case-control study., PMID:38814233
                                            Efficacy and safety of burosumab compared with conventional therapy in patients with X-linked hypophosphatemia: A systematic review., PMID:38788147
                                            Real-world non-interventional post-authorization safety study of long-term use of burosumab in children and adolescents with X-linked hypophosphatemia: first interim analysis., PMID:38764445
                                            Non-Classical Effects of FGF23: Molecular and Clinical Features., PMID:38732094
                                            S100a8/9 (S100 Calcium Binding Protein a8/9) Promotes Cardiac Hypertrophy Via Upregulation of FGF23 (Fibroblast Growth Factor 23) in Mice., PMID:38726894
                                            Recent advances in fibroblast growth factor 23-related hypophosphatemic disorders., PMID:38687287
                                            The hidden cross talk between bone and tissues through bone turnover., PMID:38634076
                                            Cardiac and Renal Fibrosis, the Silent Killer in the Cardiovascular Continuum: An Up-to-Date., PMID:38392276
                                            In chronic kidney disease altered cardiac metabolism precedes cardiac hypertrophy., PMID:38385175
                                            Hypocalcemia and Hypophosphatemia following Concurrent Denosumab Injection and Ferric Carboxymaltose Infusion in a Patient with Normal Renal Function., PMID:38343603
                                            Rickets Types and Treatment with Vitamin D and Analogues., PMID:38337700
                                            Real-world data of Brazilian adults with X-linked hypophosphatemia (XLH) treated with burosumab and comparison with other worldwide cohorts., PMID:38337160
                                            Burosumab for the treatment of cutaneous-skeletal hypophosphatemia syndrome., PMID:38229908
                                            FGF23-related hypophosphatemic rickets preceding the onset of systemic lupus erythematosus: A juvenile case., PMID:38223518
                                            Successful Burosumab Treatment in an Adult Patient with X-Linked Hypophosphatemia and Chronic Kidney Disease Stage 3b., PMID:38195892
                                            Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients., PMID:38148081
                                            The pathophysiology of hypophosphatemia., PMID:38087658