A rare coexistence: Ollier disease and primary hyperparathyroidism-mere coincidence or expanding the spectrum of Ollier disease?

Vitamin D supplementation during pregnancy: Position statement of the Groupe de Recherche et d'Information sur les Osteoporoses

Impaired organic and mineral extracellular matrix composition in early-onset osteoporosis

Marked regression of calcinosis with canakinumab in hyperphosphatemic familial tumoral calcinosis

Homozygous Loss-of-Function Variant in SLC20A1 Coding for Ubiquitous Phosphate Transporter PiT1 Is Associated With Multiple Developmental Abnormalities

Rare disease care pathways profile in France: leveraging hospital big data to characterize natural history in osteogenesis imperfecta

Management of primary hyperparathyroidism in MEN1: From initial subtotal surgery to complex treatment of the remaining gland

Chapter 3: Impact of primary hyperparathyroidism

Pregnancy-Related Complications in Osteogenesis Imperfecta

Daily or intermittent vitamin D supplementation in patients with or at risk of osteoporosis: Position statement from the GRIO

In Reply

Early-Onset Osteoporosis: Molecular Analysis in Large Cohort and Focus on the PLS3 Gene

Response to Letter to the Editor From Jagannath and Mayilvaganan: "FCH-PET/CT in Primary Hyperparathyroidism With Discordant/Negative MIBI Scintigraphy and Ultrasonography"

Trabecular bone score (TBS) in Cushing's disease: TBS gain after hypercortisolism normalization

FCH-PET/CT in Primary Hyperparathyroidism With Discordant/Negative MIBI Scintigraphy and Ultrasonography

Bone and primary hyperparathyroidism

SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients

18F-fluorocholine PET/CT and conventional imaging in primary hyperparathyroidism

Osteogenesis Imperfecta: characterization of fractures during pregnancy and post-partum

The Causes of Hypo- and Hyperphosphatemia in Humans

Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis Imperfecta

Acute anterior uveitis in spondyloarthritis: a monocentric study of 301 patients

Pre-, post- or no acidification of urine samples for calcium analysis: does it matter?

High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults

Novel function of PiT1/SLC20A1 in LPS-related inflammation and wound healing

Pro-FHH: A Risk Equation to Facilitate the Diagnosis of Parathyroid-Related Hypercalcemia

Disruption of the Phosphate Transporter Pit1 in Hepatocytes Improves Glucose Metabolism and Insulin Signaling by Modulating the USP7/IRS1 Interaction

A candidate gene study identifies a haplotype of CD2 as novel susceptibility factor for systemic sclerosis

The Case | A man with hypertension, respiratory distress, and rapidly progressive renal failure

Confirmation of CCR6 as a risk factor for anti-topoisomerase I antibodies in systemic sclerosis

Identification of NF-κB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis

Choosing the tool for osteoporosis risk prediction

Individual site-specific bone mineral density gain in normocalcemic primary hyperparathyroidism

Bone mineral density evolution after successful parathyroidectomy in patients with normocalcemic primary hyperparathyroidism

A regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosis

Performance of the assessment in Spondyloarthritis International Society classification for axial and peripheral spondyloarthritis in an established clinical cohort: comparison with criteria sets of Amor and the European Spondylarthropathy Study Group

Clinical characteristics of anterior chest wall pain in spondyloarthritis: an analysis of 275 patients

Increased risk of osteoporosis and fracture in women with systemic sclerosis: a comparative study with rheumatoid arthritis

TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients

Brief report: candidate gene study in systemic sclerosis identifies a rare and functional variant of the TNFAIP3 locus as a risk factor for polyautoimmunity

Heel pain in spondyloarthritis: results of a cross-sectional study of 275 patients

Interleukin 6 blockade in spondyloarthritis

Prevalence and clinical characteristics of psoriasis in spondyloarthritis: a descriptive analysis of 275 patients

Prevalence and characteristics of hip involvement in spondyloarthritis: a single-centre observational study of 275 patients

Prevalence and clinical characteristics of dactylitis in spondylarthritis: a descriptive analysis of 275 patients

Trabecular bone score in female patients with systemic sclerosis: comparison with rheumatoid arthritis and influence of glucocorticoid exposure

METHOFRACT, a methotrexate osteopathy multicentre cohort study

Clinical spectrum of rare bone fragility disorders and response to bisphosphonate treatment: a retrospective study

French expert consensus statement on diagnosis and management of primary hyperparathyroidism

Independent replication and meta analysis of association studies establish TNFSF4 as a susceptibility gene preferentially associated with the subset of anticentromere-positive patients with systemic sclerosis

Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review

Fatigue in spondyloarthritis: a marker of disease activity. A cross-sectional study of 266 patients