Olivia Boyer

Autosomal dominant polycystic kidney disease: the changing face of clinical management

Actualización en síndrome hemolítico urémico atípico: diagnóstico y tratamiento. Documento de consenso

Atypical hemolytic uremic syndrome

Non-Transgenic Mouse Models of Kidney Disease

Amino acid transporters revisited: New views in health and disease

Anti-complement-factor H-associated glomerulopathies

The Role of Tight Junctions in Paracellular Ion Transport in the Renal Tubule: Lessons Learned From a Rare Inherited Tubular Disorder

Critical appraisal of eculizumab for atypical hemolytic uremic syndrome

Polycystic kidney disease

Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndrome

Management of hemolytic uremic syndrome

Impaired paracellular ion transport in the loop of Henle causes familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Evaluation of Hypomagnesemia: Lessons From Disorders of Tubular Transport

Arterial hypertension during treatment with triptorelin in a child with Williams–Beuren syndrome

Heart and lung transplantation in children

Treatment of Persistent Gross Hematuria with Tranexamic Acid in Autosomal Dominant Polycystic Kidney Disease

Gorham's Disease or Massive Osteolysis

High Frequency of Acquired ADAMTS13 Deficiency After Hemolysis in Hemiscorpius Lepturus (Scorpion) Stung Children

Cystine transporter SLC7A11/xCT in cancer: ferroptosis, nutrient dependency, and cancer therapy

Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue

Clinical practice guidelines for antimicrobial prophylaxis in surgery

Chronic Kidney Disease Diagnosis and Management

Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society* Clinical Practice Guideline

Renal Control of Calcium, Phosphate, and Magnesium Homeostasis

Treatment of complex periorbital venolymphatic malformation in a neonate with a combination therapy of sirolimus and prednisolone

Neurological involvement in a child with atypical hemolytic uremic syndrome

Phenotype–genotype correlation in antenatal and neonatal variants of Bartter syndrome

Pulse Cyclophosphamide Therapy and Clinical Remission in Atypical Hemolytic Uremic Syndrome With Anti–Complement Factor H Autoantibodies

Clinical features and management of arterial hypertension in children with Williams-Beuren syndrome

Renal Transplantation Under Prophylactic Eculizumab in Atypical Hemolytic Uremic Syndrome With CFH/CFHR1 Hybrid Protein

Hemolytic Uremic Syndrome: New Developments in Pathogenesis and Treatment

Renal involvement in lysinuric protein intolerance: contribution of pathology to assessment of heterogeneity of renal lesions

Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth

Long-term remission of atypical HUS with anti-factor H antibodies after cyclophosphamide pulses

Massive Gorham-Stout syndrome of the pelvis

Improvement of Renal Function in Pediatric Heart Transplant Recipients Treated with Low-Dose Calcineurin Inhibitor and Mycophenolate Mofetil