Hypophosphatemic Rickets: Lessons from Disrupted FGF23 Control of Phosphorus Homeostasis

Effect of Paricalcitol on Circulating Parathyroid Hormone in X-Linked Hypophosphatemia: A Randomized, Double-Blind, Placebo-Controlled Study

(2014) Thomas O. Carpenter et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Randomized trial of the anti-FGF23 antibody KRN23 in X-linked hypophosphatemia

(2014) Thomas O. Carpenter et al.   JOURNAL OF CLINICAL INVESTIGATION

Phosphate Transporters and Their Function

(2013) Jürg Biber et al.   Annual Review of Physiology

Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia

(2013) Young H. Lim et al.   HUMAN MOLECULAR GENETICS

Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23-related hypophosphatemia, dental anomalies, and ectopic calcification

(2013) Silje Hjorth Rafaelsen et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Inactivation of a Novel FGF23 Regulator, FAM20C, Leads to Hypophosphatemic Rickets in Mice

(2012) Xiaofang Wang et al.   PLoS Genetics

An Atypical Degenerative Osteoarthropathy in Hyp Mice is Characterized by a Loss in the Mineralized Zone of Articular Cartilage

(2011) Guoying Liang et al.   CALCIFIED TISSUE INTERNATIONAL

Tumor-induced osteomalacia

(2011) William H Chong et al.   ENDOCRINE-RELATED CANCER

A clinician's guide to X-linked hypophosphatemia

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

Iron Modifies Plasma FGF23 Differently in Autosomal Dominant Hypophosphatemic Rickets and Healthy Humans

(2011) Erik A. Imel et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Calcitonin Administration in X-Linked Hypophosphatemia

(2011) Eva S. Liu et al.   NEW ENGLAND JOURNAL OF MEDICINE

Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice

(2011) E. G. Farrow et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Autosomal-Recessive Hypophosphatemic Rickets Is Associated with an Inactivation Mutation in the ENPP1 Gene

(2010) Varda Levy-Litan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets

(2010) Bettina Lorenz-Depiereux et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Dent's disease

(2010) Olivier Devuyst et al.   Orphanet Journal of Rare Diseases

Elevated FGF-23 and parathormone in linear nevus sebaceous syndrome with resistant rickets

(2010) Sidharth K. Sethi et al.   PEDIATRIC NEPHROLOGY

Survey of the Enthesopathy of X-Linked Hypophosphatemia and Its Characterization in Hyp Mice

(2009) Guoying Liang et al.   CALCIFIED TISSUE INTERNATIONAL

Therapeutic Effects of Anti-FGF23 Antibodies in Hypophosphatemic Rickets/Osteomalacia*

(2009) Yukiko Aono et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Dent-2 Disease: A Mild Variant of Lowe Syndrome

(2009) Arend Bökenkamp et al.   JOURNAL OF PEDIATRICS

Intestinal Npt2b Plays a Major Role in Phosphate Absorption and Homeostasis

(2009) Y. Sabbagh et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Calcimimetics as an Adjuvant Treatment for Familial Hypophosphatemic Rickets

(2008) U. S. Alon et al.   Clinical Journal of the American Society of Nephrology

A mouse model with postnatal endolymphatic hydrops and hearing loss

(2008) Cliff A. Megerian et al.   HEARING RESEARCH

McCune-Albright syndrome

(2008) Claudia E Dumitrescu et al.   Orphanet Journal of Rare Diseases

A translocation causing increased  -Klotho level results in hypophosphatemic rickets and hyperparathyroidism

(2008) C. A. Brownstein et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA