Exploring the Burden of X-Linked Hypophosphataemia: An Opportunistic Qualitative Study of Patient Statements Generated During a Technology Appraisal

Risk of cardiovascular involvement in pediatric patients with X-linked hypophosphatemia

(2019) Olaya Hernández-Frías et al.   PEDIATRIC NEPHROLOGY

FGF23 and its role in X-linked hypophosphatemia-related morbidity

(2019) Signe Sparre Beck-Nielsen et al.   Orphanet Journal of Rare Diseases

X-linked hypophosphatemia: Management and treatment prospects

(2019) Anne-Sophie Lambert et al.   JOINT BONE SPINE

C-Terminal Fibroblast Growth Factor-23 Levels in Non-Nutritional Hypophosphatemic Rickets

(2019) Joyita Bharati et al.   INDIAN JOURNAL OF PEDIATRICS

Elevated Bone Remodeling Markers of CTX and P1NP in Addition to Sclerostin in Patients with X-linked Hypophosphatemia: A Cross-Sectional Controlled Study

(2019) Stinus Hansen et al.   CALCIFIED TISSUE INTERNATIONAL

Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia

(2019) Cong Zhang et al.   BONE

Rickets severity predicts clinical outcomes in children with X-linked hypophosphatemia: Utility of the radiographic Rickets Severity Score

(2019) Tom D. Thacher et al.   BONE

Impaired mineral quality in dentin in X-linked hypophosphatemia

(2018) Benjamin R. Coyac et al.   CONNECTIVE TISSUE RESEARCH

Lung function decline is delayed but not decreased in patients with cystic fibrosis and the R117H gene mutation

(2018) Jeffrey S. Wagener et al.   Journal of Cystic Fibrosis

Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations

(2018) Douglas Chesher et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Burosumab Therapy in Children with X-Linked Hypophosphatemia

(2018) Thomas O. Carpenter et al.   NEW ENGLAND JOURNAL OF MEDICINE

Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3

(2018) Sezer Acar et al.   PLoS One

Qualitative Research to Explore the Patient Experience of X-Linked Hypophosphatemia and Evaluate the Suitability of the BPI-SF and WOMAC® as Clinical Trial End Points

(2018) Christina Theodore-Oklota et al.   VALUE IN HEALTH

Genetic analysis of three families with X-linked dominant hypophosphatemic rickets

(2018) Xinfu Lin et al.   JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM

Hormonal Regulation of Osteocyte Perilacunar and Canalicular Remodeling in the Hyp Mouse Model of X-Linked Hypophosphatemia

(2017) Danielle Tokarz et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Therapeutic management of hypophosphatemic rickets from infancy to adulthood

(2014) Agnès Linglart et al.   Endocrine Connections

A clinician's guide to X-linked hypophosphatemia

(2011) Thomas O Carpenter et al.   JOURNAL OF BONE AND MINERAL RESEARCH