1. Defective Mineralization in X-Linked Hypophosphatemia Dental Pulp Cell Cultures
    B.R. Coyac et al, 2018, Journal of Dental Research CrossRef
  2. Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia
    Cong Zhang et al, 2019, Bone CrossRef
  3. A pathogenic PHEX variant (c.1483-1G>C) in a Korean patient with X-linked hypophosphatemic rickets
    In Hwa Jeong et al, 2021, Annals of Pediatric Endocrinology & Metabolism CrossRef
  4. Novel variants and uncommon cases among southern Chinese children with X-linked hypophosphatemia
    Y. Lin et al, 2020, Journal of Endocrinological Investigation CrossRef
  5. Clinical and Genetic Characteristics of 153 Chinese Patients With X-Linked Hypophosphatemia
    Xiaoyun Lin et al, 2021, Frontiers in Cell and Developmental Biology CrossRef
  6. X-linked hypophosphataemic rickets: Report of a novel PHEX mutation and cinacalcet as adjuvant therapy in the mineral metabolism control
    Daniela Cavaco et al, 2022, Modern Rheumatology Case Reports CrossRef
  7. PHEX Gene Mutation in a Patient with X-Linked Hypophosphatemic Rickets in a Developing Country


    Jessica María Forero-Delgadillo et al, 2020, The Application of Clinical Genetics CrossRef
  8. De Novo Large Deletions in the PHEX Gene Caused X-Linked Hypophosphataemic Rickets in Two Italian Female Infants Successfully Treated with Burosumab
    Carmine Pecoraro et al, 2023, Diagnostics CrossRef
  9. Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia
    Tian Xu et al, 2022, Frontiers in Endocrinology CrossRef
  10. The Variant p.Ala84Pro Is Causative of X-Linked Hypophosphatemic Rickets: Possible Relationship with Burosumab Swinging Response in Adults
    Maria Carmela Zagari et al, 2022, Genes CrossRef
  11. Asia‐Pacific Consensus Recommendations on X‐Linked Hypophosphatemia: Diagnosis, Multidisciplinary Management, and Transition From Pediatric to Adult Care
    Craig F Munns et al, 2023, JBMR Plus CrossRef
  12. Oral Manifestations of Systemic Disease
    Brad W. Neville et al, 2019, Color Atlas of Oral and Maxillofacial Diseases CrossRef
  13. Molecular and Biochemical Aspects of Hypophosphatemic Rickets; an Updated Review
    Fateme Asadzadeh Manjili et al, 2017, International Journal of Basic Science in Medicine CrossRef
  14. X-linked Hypophosphatemic Rickets, del(2)(q37.1;q37.3) Deletion Syndrome and Mosaic Turner Syndrome, mos 45,X/46,X, del(2)(q37.1;q37.3) in a 3-year-old Female
    Alaina P. Vidmar et al, 2017, Journal of Bone Metabolism CrossRef
  15. Targeted resequencing of phosphorus metabolism‑related genes in 86 patients with hypophosphatemic rickets/osteomalacia
    Jiemei Gu et al, 2018, International Journal of Molecular Medicine CrossRef
  16. Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription
    Yu-mian Gan et al, 2022, Cell Death & Disease CrossRef
  17. Pathogenic Variants of the PHEX Gene
    Yasuhisa Ohata et al, 2022, Endocrines CrossRef
  18. Whole exome sequencing identifies two novel variants in PHEX and DMP1 in Malaysian children with hypophosphatemic rickets
    Nahid Tavana et al, 2022, Italian Journal of Pediatrics CrossRef
  19. Rare, genetically conditioned forms of rickets: Differential diagnosis and advances in diagnostics and treatment
    I. Michałus et al, 2018, Clinical Genetics CrossRef
  20. Diagnosis, treatment-monitoring and follow-up of children and adolescents with X-linked hypophosphatemia (XLH)
    Anya Rothenbuhler et al, 2020, Metabolism CrossRef
  21. New Technologies in Pre- and Postnatal Diagnosis
    Anne-Marie Laberge et al, 2020, Maternal-Fetal and Neonatal Endocrinology CrossRef
  22. Identification of six novel variants from nine Chinese families with hypophosphatemic rickets
    Yixuan Cao et al, 2022, BMC Medical Genomics CrossRef
  23. Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf Cooperation Council countries
    Fahad Al Juraibah et al, 2021, Archives of Osteoporosis CrossRef