J. Bacchetta

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From bone abnormalities to mineral metabolism dysregulation in autosomal dominant polycystic kidney disease

D. Mekahli, J. Bacchetta, 2013, Pediatric Nephrology.

Calcium isotope fractionation by osteoblasts and osteoclasts, across endothelial and epithelial cell barriers and with binding to proteins.

J. Bacchetta, S. Zarogiannis, A. Eisenhauer, 2021, American journal of physiology. Regulatory, integrative and comparative physiology.

Standardization of pediatric uroradiological terms: A multidisciplinary European glossary.

M. Riccabona, H. Mentzel, J. Bacchetta, 2017, Journal of Pediatric Urology.

Standardization of pediatric uroradiological terms: a multidisciplinary European glossary

M. Riccabona, H. Mentzel, J. Bacchetta, 2017, Pediatric Radiology.

[Post-diarrheal haemolytic uremic syndrome: when shall we consider it? Which follow-up?].

J. Bacchetta, B. Ranchin, A. Belot, 2011, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

biophysical basis of homeostasis Intrarenal oxygenation: unique challenges and the

David W. Smith, J. Stokes, M. Janier, 2011 .

Suppression of iron-regulatory hepcidin by vitamin D.

J. Bacchetta, B. Hollis, I. Salusky, 2014, Journal of the American Society of Nephrology : JASN.

Low incidence of SARS-CoV-2, risk factors of mortality and the course of illness in the French national cohort of dialysis patients

E. M. Passos, L. Duflot, M. Brahimi, 2020, Kidney International.

Long‐term critical issues in pediatric renal transplant recipients: a single‐center experience

J. Bacchetta, B. Ranchin, R. Bouvier, 2013, Transplant international : official journal of the European Society for Organ Transplantation.

Primary disease recurrence—effects on paediatric renal transplantation outcomes

J. Bacchetta, P. Cochat, 2015, Nature Reviews Nephrology.

CKD-MBD after kidney transplantation

J. Bacchetta, K. Wesseling-Perry, K. Wesseling‐Perry, 2011, Pediatric Nephrology.

Disseminated bartonellosis in a child with steroid-dependent nephrotic syndrome receiving mycophenolate mofetil monotherapy.

J. Bacchetta, B. Ranchin, L. Viremouneix, 2021, Nephrologie & therapeutique.

European Consensus Statement on the diagnosis and management of osteoporosis in chronic kidney disease stages G4-G5D.

M. Vervloet, P. D’Haese, G. Spasovski, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[Diagnosis and management of chronic kidney disease in children: Guidelines of the French Society of Pediatric Nephrology].

J. Bacchetta, G. Deschênes, R. Vieux, 2016, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Immune, metabolic and epidemiological aspects of vitamin D in chronic kidney disease and transplant patients.

J. Bacchetta, D. Fouque, G. Jean, 2014, Clinical biochemistry.

Bone evaluation in paediatric chronic kidney disease: Clinical practice points from the European Society for Paediatric Nephrology CKD-MBD and Dialysis working groups and CKD-MBD working group of the ERA-EDTA.

D. Haffner, J. Bacchetta, J. Groothoff, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia

L. Rejnmark, P. Wicart, D. Eastwood, 2019, Nature Reviews Nephrology.

Cinacalcet use in paediatric dialysis: a position statement from the European Society for Paediatric Nephrology and the Chronic Kidney Disease-Mineral and Bone Disorders Working Group of the ERA-EDTA.

M. Vervloet, D. Haffner, J. Bacchetta, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Clinical practice recommendations for native vitamin D therapy in children with chronic kidney disease Stages 2-5 and on dialysis.

A. Edefonti, N. Bishop, D. Fischer, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Clinical practice recommendations for treatment with active vitamin D analogues in children with chronic kidney disease Stages 2-5 and on dialysis.

A. Edefonti, D. Haffner, J. Bacchetta, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Association between 25(OH) vitamin D and graft survival in renal transplanted children

R. Salomon, N. Garcelon, F. Bienaimé, 2020, Pediatric transplantation.

Antibacterial Responses by Peritoneal Macrophages Are Enhanced Following Vitamin D Supplementation

J. Bacchetta, A. Rastogi, S. Leroy, 2014, PloS one.

[Weakening osteopathies, chronic kidney disease, malabsorption, biological anomalies of calium/phosphorus metabolism: appropriate indications for a reasoned reimbursment of serum vitamin D measurement].

P. Chanson, C. Annweiler, O. Beauchet, 2014, Annales de biologie clinique.

The interplay between bone and vessels in pediatric CKD: lessons from a single-center study

J. Bacchetta, A. Doyon, B. Ranchin, 2018, Pediatric Nephrology.

Early impairment of trabecular microarchitecture assessed with HR‐pQCT in patients with stage II‐IV chronic kidney disease

P. Delmas, J. Bacchetta, L. Juillard, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Bone imaging and chronic kidney disease: will high-resolution peripheral tomography improve bone evaluation and therapeutic management?

P. Delmas, J. Bacchetta, L. Juillard, 2009, Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation.

Towards adulthood with a solitary kidney

J. Bacchetta, E. Bérard, P. Cochat, 2018, Pediatric Nephrology.

Evidence for Bone and Mineral Metabolism Alterations in Children With Autosomal Dominant Polycystic Kidney Disease

D. Mekahli, J. Bacchetta, E. Levtchenko, 2017, The Journal of clinical endocrinology and metabolism.

Adherence to cysteamine in nephropathic cystinosis: A unique electronic monitoring experience for a better understanding. A prospective cohort study: CrYSTobs

J. Bacchetta, B. Ranchin, G. Deschênes, 2020, Pediatric Nephrology.

Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D

J. Bacchetta, S. Lemoine, Glenville Jones, 2021, Frontiers in Endocrinology.

Genetic, Environmental, and Disease-Associated Correlates of Vitamin D Status in Children with CKD.

A. Anarat, A. Köttgen, J. Bacchetta, 2016, Clinical journal of the American Society of Nephrology : CJASN.

Which creatinine and cystatin C equations can be reliably used in children?

J. Bacchetta, B. Ranchin, P. Cochat, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Both extrauterine and intrauterine growth restriction impair renal function in children born very preterm.

J. Bacchetta, G. Putet, P. Cochat, 2009, Kidney international.

Copper Isotope Evidence of Oxidative Stress–Induced Hepatic Breakdown and the Transition to Hepatocellular Carcinoma

F. Zoulim, J. Bacchetta, Marie-Laure Plissonnier, 2022, Gastro Hep Advances.

Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper.

J. Bacchetta, A. Lapillonne, G. Laverny, 2022, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Fluconazole in hypercalciuric patients with increased 1,25(OH)2D levels: the prospective, randomized, placebo-controlled, double-blind FLUCOLITH trial

J. Bacchetta, S. Lemoine, F. Subtil, 2022, Trials.

Fluconazole as a New Therapeutic Tool to Manage Patients With NPTIIc (SLC34A3) Mutation: A Case Report.

J. Bacchetta, S. Lemoine, N. Tram, 2019, American journal of kidney diseases : the official journal of the National Kidney Foundation.

CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.

J. Bacchetta, G. Deschênes, J. Souberbielle, 2015, The Journal of clinical endocrinology and metabolism.

[Vitamin D supplementation: not too much, not too little!].

J. Bacchetta, C. Vuillerot, P. Cochat, 2015, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Inactivation of Osteoblast PKC Signaling Reduces Cortical Bone Mass and Density and Aggravates Renal Osteodystrophy in Mice with Chronic Kidney Disease on High Phosphate Diet

J. Bacchetta, F. Schaefer, S. Bahram, 2022, International journal of molecular sciences.

Bone marrow adiposity inversely correlates with bone turnover in pediatric renal osteodystrophy

J. Bacchetta, R. Pereira, I. Salusky, 2021, Bone reports.

Title Idiopathic juvenile osteoporosis : a cross-sectional single-centre experience with bone histomorphometry and quantitative computed tomography Permalink

J. Bacchetta, R. Pereira, V. Gilsanz, 2013 .

Idiopathic juvenile osteoporosis: a cross-sectional single-centre experience with bone histomorphometry and quantitative computed tomography

J. Bacchetta, R. Pereira, V. Gilsanz, 2013, Pediatric Rheumatology.

The skeletal consequences of growth hormone therapy in dialyzed children: a randomized trial.

R. Elashoff, J. Bacchetta, He-jing Wang, 2013, Clinical journal of the American Society of Nephrology : CJASN.

Chronic Kidney Disease – Mineral and Bone Disorder (CKD-MBD)

J. Bacchetta, R. Shroff, K. Wesseling-Perry, 2021, Pediatric Nephrology.

Intermittent Bi-Daily Sub-cutaneous Teriparatide Administration in Children With Hypoparathyroidism: A Single-Center Experience

J. Bacchetta, S. Lemoine, R. Chapurlat, 2021, Frontiers in Pediatrics.

Assessment of mineral and bone biomarkers highlights a high frequency of hypercalciuria in asymptomatic healthy teenagers

J. Bacchetta, B. Ranchin, L. Dubourg, 2019, Acta paediatrica.

Physiology of FGF23 and overview of genetic diseases associated with renal phosphate wasting.

J. Bacchetta, D. Prié, C. Bardet, 2020, Metabolism: clinical and experimental.

[FGF23 and Klotho: the new cornerstones of phosphate/calcium metabolism].

J. Bacchetta, I. Salusky, P. Cochat, 2011, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

The effect of lumasiran therapy for primary hyperoxaluria type 1 in small infants

J. Bacchetta, J. Harambat, A. Sellier-Leclerc, 2022, Pediatric Nephrology.

Long-Term Transplantation Outcomes in Patients With Primary Hyperoxaluria Type 1 Included in the European Hyperoxaluria Consortium (OxalEurope) Registry

J. Bacchetta, B. Hoppe, N. Mohebbi, 2021, Kidney International Reports.

The combined use of creatinine and cystatin C improves the detection of renal dysfunction in children undergoing home parenteral nutrition.

J. Bacchetta, N. Peretti, Emmanuelle Ecochard-Dugelay, 2021, JPEN. Journal of parenteral and enteral nutrition.

Treatment by immunoadsorption for recurrent focal segmental glomerulosclerosis after paediatric kidney transplantation: a multicentre French cohort

R. Salomon, J. Bacchetta, G. Deschênes, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The Management of CKD-MBD in Pediatric Dialysis Patients

J. Bacchetta, I. Salusky, 2021 .

Bone Disease in Nephropathic Cystinosis: Beyond Renal Osteodystrophy

J. Bacchetta, S. Gaillard, I. Machuca‐Gayet, 2020, International journal of molecular sciences.

Hyperphosphatemia and Chronic Kidney Disease: A Major Daily Concern Both in Adults and in Children

J. Bacchetta, B. Ranchin, J. Bernardor, 2020, Calcified Tissue International.

Treatment of hyperphosphatemia: the dangers of high PTH levels

J. Bacchetta, 2019, Pediatric Nephrology.

Bone biopsy practice patterns across Europe: the European renal osteodystrophy initiative—a position paper

G. Spasovski, J. Bacchetta, Aníbal Ferreira, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Vitamin D in Children with Chronic Kidney Disease: A Focus on Longitudinal Bone Growth

J. Bacchetta, I. Salusky, 2016 .

Markers of Bone Metabolism Are Affected by Renal Function and Growth Hormone Therapy in Children with Chronic Kidney Disease

D. Fischer, D. Haffner, J. Bacchetta, 2015, PloS one.

[Mineral and bone disorders in renal transplantation].

J. Bacchetta, R. Chapurlat, M. Lafage-Proust, 2013, Nephrologie & therapeutique.

The consequences of pediatric renal transplantation on bone metabolism and growth

J. Bacchetta, B. Ranchin, D. Demède, 2013, Current opinion in organ transplantation.

Hemodiafiltration Is Associated With Reduced Inflammation and Increased Bone Formation Compared With Conventional Hemodialysis in Children: The HDF, Hearts and Heights (3H) Study

A. Anarat, M. Litwin, D. Fischer, 2021, Kidney international reports.

The influence of glomerular filtration rate and age on fibroblast growth factor 23 serum levels in pediatric chronic kidney disease.

J. Bacchetta, B. Ranchin, S. Arnaud, 2010, The Journal of clinical endocrinology and metabolism.

Bone metabolism in oxalosis: a single-center study using new imaging techniques and biomarkers

J. Bacchetta, B. Dohin, S. Boutroy, 2010, Pediatric Nephrology.

The relationship between adipokines, osteocalcin and bone quality in chronic kidney disease.

J. Bacchetta, J. Drai, L. Juillard, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Paraneoplastic glomerular diseases and malignancies.

J. Bacchetta, J. Droz, L. Juillard, 2009, Critical reviews in oncology/hematology.

What about the renal function during childhood of children born from dialysed mothers?

J. Bacchetta, P. Cochat, F. Guebre-egziabher, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Fibroblast growth factor 23 inhibits extrarenal synthesis of 1,25‐dihydroxyvitamin D in human monocytes

J. Bacchetta, J. Adams, I. Salusky, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The Relationship Between Body Composition and Bone Quality Measured with HR-pQCT in Peritoneal Dialysis Patients

J. Bacchetta, J. Drai, D. Fouque, 2017, Peritoneal Dialysis International.

Local protocol helped to deliver vitamin D levels more accurately in preterm infants

J. Bacchetta, M. Butin, F. Plaisant, 2021, Acta paediatrica.

A prospective case–control pilot study to evaluate bone microarchitecture in children and teenagers on long-term parenteral nutrition using HR-pQCT

J. Bacchetta, N. Peretti, C. Confavreux, 2021, Scientific Reports.

Children and adolescents with cystic fibrosis display moderate bone microarchitecture abnormalities: data from high-resolution peripheral quantitative computed tomography

J. Bacchetta, J. Drai, R. Chapurlat, 2017, Osteoporosis International.

Novel PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease (ADPKD)

J. Bacchetta, B. Ranchin, J. Berthiller, 2011 .

High Incidence of Cranial Synostosis and Chiari I Malformation in Children With X‐Linked Hypophosphatemic Rickets (XLHR)

C. Adamsbaum, J. Bacchetta, F. Di Rocco, 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Intermittent cholecalciferol supplementation in children and teenagers followed in pediatric nephrology: data from a prospective single-center single-arm open trial

J. Bacchetta, B. Ranchin, A. Sellier-Leclerc, 2019, European Journal of Pediatrics.

Cardiac involvement in pediatric hemolytic uremic syndrome

J. Bacchetta, E. Javouhey, J. Rambaud, 2022, Pediatric Nephrology.

Idiopathic nephrotic syndrome relapse following COVID-19 vaccination: a series of 25 cases

J. Bacchetta, B. Ranchin, A. Servais, 2022, Clinical kidney journal.

Guidelines for the management of children at risk of secondary bone fragility: Expert opinion of a French working group.

J. Salles, J. Bacchetta, E. Dugelay, 2020, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Renal Prognosis in Children With Tubulointerstitial Nephritis and Uveitis Syndrome

J. Bacchetta, J. Hogan, F. Broux, 2021, Kidney International Reports.

Active vitamin D is cardioprotective in experimental uraemia but not in children with CKD Stages 3-5.

D. Fischer, D. Haffner, J. Bacchetta, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Beyond mineral metabolism, is there an interplay between FGF23 and vitamin D in innate immunity?

J. Bacchetta, I. Salusky, M. Hewison, 2013, Pediatric Nephrology.

The case: familial renal failure with ocular abnormality.

J. Bacchetta, P. Cochat, A. Liutkus, 2008, Kidney international.

[Multicystic dysplastic kidney disease: update and information for parents at the time of prenatal diagnosis].

J. Bacchetta, H. Dodat, P. Cochat, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Demographic Characteristics, Risk Factors, and Presenting Features of Children with Symptomatic Nutritional Rickets: A French Series

J. Salles, J. Bacchetta, A. Rothenbuhler, 2020, Hormone Research in Paediatrics.

FGF23 and infectious diseases

J. Bacchetta, M. Hewison, 2021 .

Rare diseases of phosphate and calcium metabolism: crossing glances between nephrology and endocrinology.

J. Bacchetta, S. Lemoine, A. Bertholet-Thomas, 2020, Annales d'endocrinologie.

Hyperphosphatemic tumoral calcinosis caused by FGF23 compound heterozygous mutations: what are the therapeutic options for a better control of phosphatemia?

J. Bacchetta, F. Chotel, F. Dijoud, 2018, Pediatric Nephrology.

Teenagers and young adults with a past of allogenic hematopoietic stem cell transplantation are at significant risk of chronic kidney disease

Y. Bertrand, J. Bacchetta, C. Domenech, 2021, Pediatric Nephrology.

An Expert Perspective on Phosphate Dysregulation With a Focus on Chronic Hypophosphatemia

O. Mäkitie, M. Vervloet, M. Brandi, 2021, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Orthopedic and neurosurgical care of X-linked hypophosphatemia.

C. Adamsbaum, S. Pannier, P. Wicart, 2021, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Tyrosinemia type 1 in pediatric nephrology: Not always straightforward.

J. Bacchetta, M. Butin, A. Fouilhoux, 2021, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Cinacalcet studies in pediatric subjects with secondary hyperparathyroidism receiving dialysis

J. Bacchetta, F. Schaefer, B. Warady, 2020, Pediatric Nephrology.

Neonatal transient hypophosphatemic hypercalciuric rickets in dizygous twins: A role for maternal alendronate therapy before pregnancy or antireflux medications?

J. Bacchetta, P. Cochat, O. Claris, 2016, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Vitamin D deficiency is associated with mortality in maintenance dialysis: moving forward from epidemiology to clinical trials.

J. Bacchetta, S. Pelletier, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

FGF23 in chronic kidney disease: are we lost in translation?

J. Bacchetta, 2016, BoneKEy reports.

Biphasic Effects of Vitamin D and FGF23 on Human Osteoclast Biology

J. Bacchetta, P. Jurdic, I. Machuca‐Gayet, 2015, Calcified Tissue International.

Combining exercise and growth hormone therapy: how can we translate from animal models to chronic kidney disease children?

J. Bacchetta, I. Salusky, 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Naturally occurring stable calcium isotope ratios are a novel biomarker of bone calcium balance in chronic kidney disease.

D. Fischer, J. Bacchetta, A. Jankauskienė, 2022, Kidney international.

Pediatric urolithiasis: what can pediatricians expect from radiologists?

J. Bacchetta, S. Cabet, V. Bidault, 2022, Pediatric Radiology.

Vitamine D : une hormone d’intérêt général

J. Bacchetta, J. Bacchetta, 2013 .

RMND1 mutations in two siblings: Severe renal hypoplasia but different levels of extrarenal abnormality severity: The ethics of decision making.

J. Bacchetta, B. Ranchin, D. Ville, 2019, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Troubles du comportement alimentaire : pensons à l’ostéoprotection !

J. Bacchetta, J. Bacchetta, C. Freychet, 2015 .

[Pediatric eating disorders: Do not forget to protect bones!].

J. Bacchetta, C. Freychet, 2015, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Determinants of Statural Growth in European Children With Chronic Kidney Disease: Findings From the Cardiovascular Comorbidity in Children With Chronic Kidney Disease (4C) Study

A. Anarat, J. Bacchetta, F. Schaefer, 2019, Front. Pediatr..

Precocious puberty and unlicensed paediatric drugs for severe hyperparathyroidism.

J. Bacchetta, B. Ranchin, M. Nicolino, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Big data and outcomes in paediatric haemodialysis: how can nephrologists use these new tools in daily practice?

D. Maucort-Boulch, J. Bacchetta, B. Ranchin, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Uric acid and IGF1 as possible determinants of FGF23 metabolism in children with normal renal function

J. Bacchetta, I. Salusky, K. Wesseling-Perry, 2012, Pediatric Nephrology.

Muscle and Bone Impairment in Infantile Nephropathic Cystinosis: New Concepts

D. Haffner, J. Bacchetta, M. Leifheit-Nestler, 2022, Cells.

Bone assessment in children with chronic kidney disease: data from two new bone imaging techniques in a single-center pilot study

J. Bacchetta, B. Ranchin, S. Boutroy, 2011, Pediatric Nephrology.

Efficacy of extracorporeal albumin dialysis for acute kidney injury due to cholestatic jaundice nephrotoxicity

J. Bacchetta, L. Juillard, F. Sens, 2016, BMJ Case Reports.

Inherited renal tubular dysgenesis: the first patients surviving the neonatal period

O. Gribouval, M. Gubler, J. Bacchetta, 2008, European Journal of Pediatrics.

[PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD): Genotype-phenotype correlations from a series of 308 cases to improve prenatal counselling].

J. Bacchetta, B. Ranchin, L. Michel-Calemard, 2018, Nephrologie & therapeutique.

Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

F. Trepiccione, P. Houillier, L. Weber, 2022, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The use of cinacalcet after pediatric renal transplantation: an international CERTAIN Registry analysis

B. Tönshoff, J. Bacchetta, C. Schmitt, 2020, Pediatric Nephrology.

Hyperphosphatemia and Chronic Kidney Disease: A Major Daily Concern Both in Adults and in Children

J. Bacchetta, B. Ranchin, J. Bernardor, 2020, Calcified Tissue International.

Inhibition of Osteoclast Differentiation by 1.25‐D and the Calcimimetic KP2326 Reveals 1.25‐D Resistance in Advanced CKD

J. Bacchetta, B. Ranchin, O. Peyruchaud, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Bone disease in nephropathic cystinosis is related to cystinosin-induced osteoclastic dysfunction

J. Bacchetta, P. Cochat, O. Peyruchaud, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Teenagers and young adults with nephropathic cystinosis display significant bone disease and cortical impairment

J. Bacchetta, G. Deschênes, P. Szulc, 2018, Pediatric Nephrology.

Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?

J. Bacchetta, B. Ranchin, M. Zenker, 2018, Bone.

Pediatric combined liver–kidney transplantation: a single-center experience of 18 cases

J. Bacchetta, R. Dubois, L. Badet, 2016, Pediatric Nephrology.

Bone impairment in oxalosis: An ultrastructural bone analysis.

J. Bacchetta, G. Boivin, P. Cochat, 2015, Bone.

Bone impairment in primary hyperoxaluria: a review

J. Bacchetta, G. Boivin, P. Cochat, 2015, Pediatric Nephrology.

Nephropathic cystinosis--a gap between developing and developed nations.

V. Tasic, J. Bacchetta, P. Cochat, 2014, The New England journal of medicine.

Pediatric bone evaluation with HR-pQCT: A comparison between standard and height-adjusted positioning protocols in a cohort of teenagers with chronic kidney disease.

J. Bacchetta, B. Ranchin, R. Chapurlat, 2019, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Improving Clinical Care for Children With CKD: A Report From a National Kidney Foundation Scientific Workshop.

J. Flynn, D. Haffner, J. Bacchetta, 2022, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Hyperparathyroidism Is an Independent Risk Factor for Allograft Dysfunction in Pediatric Kidney Transplantation

L. Weber, B. Tönshoff, D. Haffner, 2022, Kidney international reports.

Off-label use of cinacalcet in pediatric primary hyperparathyroidism: A French multicenter experience

J. Salles, J. Bacchetta, M. Castanet, 2022, Frontiers in Pediatrics.

FGF23 and paediatric transplantation: a single-centre French experience.

J. Bacchetta, B. Ranchin, P. Cochat, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Management of children with congenital nephrotic syndrome: challenging treatment paradigms.

A. Edefonti, J. Bacchetta, G. Ariceta, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Primary hyperoxaluria type 1: novel therapies at a glance

J. Lieske, J. Bacchetta, 2022, Clinical kidney journal.

[Relationship between glomerular filtration rate, uric acid, and parathyroid hormone in children].

J. Bacchetta, B. Ranchin, P. Cochat, 2013, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

CARPEDIEM® for continuous kidney replacement therapy in neonates and small infants: a French multicenter retrospective study

J. Bacchetta, B. Ranchin, D. De Luca, 2023, Pediatric Nephrology.

Genetic assessment in primary hyperoxaluria: why it matters

J. Bacchetta, J. Groothoff, G. Mandrile, 2022, Pediatric Nephrology.

Nephrolithiasis related to inborn metabolic diseases

M. Daudon, J. Bacchetta, P. Cochat, 2009, Pediatric Nephrology.

Composition of urinary stones in children: clinical and metabolic determinants in a French tertiary care center

J. Bacchetta, C. Machon, A. Bertholet-Thomas, 2021, European Journal of Pediatrics.

The interest of oral calcium loads test in the diagnosis and management of pediatric nephrolithiasis with hypercalciuria: Experience from a tertiary pediatric centre.

J. Bacchetta, S. Lemoine, C. Machon, 2020, Journal of pediatric urology.

Impact of a change in protected environment on the occurrence of severe bacterial and fungal infections in children undergoing hematopoietic stem cell transplantation

J. Bacchetta, Y. Bertrand, C. Ploton, 2016, European journal of haematology.

Worldwide view of nephropathic cystinosis: results from a survey from 30 countries

V. Tasic, J. Ehrich, J. Bacchetta, 2017, BMC Nephrology.

Management of bone disease in cystinosis: Statement from an international conference

W. Gahl, O. Greil, D. Haffner, 2019, Journal of inherited metabolic disease.

Clinical practice recommendations for growth hormone treatment in children with chronic kidney disease

A. Edefonti, B. Tönshoff, D. Haffner, 2019, Nature Reviews Nephrology.

Response to Cysteamine in Osteoclasts Obtained from Patients with Nephropathic Cystinosis: A Genotype/Phenotype Correlation

J. Bacchetta, J. Hogan, S. Lemoine, 2021, Cells.

Skeletal implications and management of cystinosis: three case reports and literature review.

J. Bacchetta, F. Emma, G. Boivin, 2016, BoneKEy reports.

Bone mineral density and growth changes in patients with distal renal tubular acidosis after two-years treatment with a new alkalizing drug (ADV7103).

J. Bacchetta, C. Guittet, L. Granier, 2022, Nefrologia.

Treatment and outcome of congenital nephrotic syndrome

R. Salomon, O. Gribouval, J. Bacchetta, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Pediatric combined liver–kidney transplantation: a 2015 update

D. Mekahli, J. Bacchetta, C. Rivet, 2015, Current opinion in organ transplantation.

Paediatric liver transplanted patients and prevalence of hepatitis E virus.

J. Dumortier, J. Bacchetta, O. Boillot, 2015, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Non-drug-induced nephrotoxicity

J. Bacchetta, L. Juillard, P. Cochat, 2009, Pediatric Nephrology.

Severe voiding dysfunction: ask the child to smile.

J. Bacchetta, P. Cochat, 2010, Kidney international.

Evaluation of hypophosphatemia: lessons from patients with genetic disorders.

J. Bacchetta, I. Salusky, 2012, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Maternal Transmission Ratio Distortion of GNAS Loss‐of‐Function Mutations

L. Faivre, J. Bacchetta, M. Gérard, 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Osteocalcin Signaling in Myofibers Is Necessary and Sufficient for Optimum Adaptation to Exercise.

R. de Cabo, R. Kitsis, R. Friedman, 2016, Cell metabolism.

Pediatric renal transplantation: A retrospective single‐center study on epidemiology and morbidity due to EBV

J. Bacchetta, B. Lina, B. Kassai, 2018, Pediatric transplantation.

Infants with congenital nephrotic syndrome have comparable outcomes to infants with other renal diseases

A. Edefonti, J. Bacchetta, G. Ariceta, 2018, Pediatric Nephrology.

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1

K. Dahan, P. Houillier, X. Jeunemaître, 2015, Human mutation.

C3 glomerulopathy and eculizumab: a report on four paediatric cases

J. Bacchetta, F. Dijoud, V. Frémeaux-Bacchi, 2017, Pediatric Nephrology.

Peripheral Blood Mononuclear Cells (PBMCs) to Dissect the Underlying Mechanisms of Bone Disease in Chronic Kidney Disease and Rare Renal Diseases

J. Bacchetta, O. Peyruchaud, I. Machuca‐Gayet, 2021, Current Osteoporosis Reports.

Early-onset hypoparathyroidism and chronic keratitis revealing APECED

J. Bacchetta, A. Belot, A. Weetman, 2015, Clinical case reports.

[Interferent RNA treatment: Example of primary hyperoxaluria].

J. Bacchetta, P. Cochat, A. Sellier-Leclerc, 2021, Nephrologie & therapeutique.

Improved Outcome of Infantile Oxalosis Over Time in Europe: Data From the OxalEurope Registry

E. Salido, J. Bacchetta, B. Hoppe, 2022, Kidney international reports.

Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope

B. Knebelmann, J. Bacchetta, J. Groothoff, 2023, Nature Reviews Nephrology.

Renal function can be impaired in children with primary hyperoxaluria type 3

J. Bacchetta, F. Cachat, P. Cochat, 2015, Pediatric Nephrology.

Assessment of hand bone loss in rheumatoid arthritis by high-resolution peripheral quantitative CT

Nicolas Vilayphiou, Hubert Marotte, P. Delmas, 2010, Annals of the rheumatic diseases.

Diagnosis and management of mineral and bone disorders in infants with CKD: clinical practice points from the ESPN CKD-MBD and Dialysis working groups and the Pediatric Renal Nutrition Taskforce

D. Haffner, J. Bacchetta, B. Ranchin, 2023, Pediatric Nephrology.

Craniosynostosis and metabolic bone disorder. A review.

C. Adamsbaum, J. Bacchetta, F. Di Rocco, 2019, Neuro-Chirurgie.

Renal transplantation in children under 3 years of age: Experience from a single‐center study

J. Bacchetta, B. Ranchin, F. Baudin, 2018, Pediatric transplantation.

Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

N. Boddaert, D. Magen, P. Revy, 2019, Nature Communications.

‘Renal hypersensitivity’ to inulin and IgA nephropathy

J. Bacchetta, R. Bouvier, P. Cochat, 2008, Pediatric Nephrology.

Congenital versus acquired solitary kidney: is the difference relevant?

J. Bacchetta, B. Ranchin, P. Cochat, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

The consequences of chronic kidney disease on bone metabolism and growth in children.

J. Bacchetta, I. Salusky, K. Wesseling-Perry, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Discontinuation of RAAS Inhibition in Children with Advanced CKD.

D. de Zeeuw, H. Heerspink, J. Bacchetta, 2020, Clinical journal of the American Society of Nephrology : CJASN.

Developing Consensus-Based Outcome Domains for Trials in Children and Adolescents With CKD: An International Delphi Survey.

A. Teixeira-Pinto, J. Craig, M. Howell, 2020, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Circulating autotaxin levels in healthy teenagers: Data from the Vitados cohort

J. Bacchetta, M. Legrand, O. Peyruchaud, 2023, Frontiers in Pediatrics.

Long-term outcomes of peritoneal dialysis started in infants below 6 months of age: An experience from two tertiary centres.

J. Bacchetta, B. Ranchin, P. Cochat, 2020, Nephrologie & therapeutique.

Review: Neonatal dialysis is technically feasible but ethical and global issues need to be addressed

J. Bacchetta, B. Ranchin, E. Javouhey, 2020, Acta paediatrica.

Patient and transplant outcome in infants starting renal replacement therapy before 2 years of age

J. Bacchetta, J. Hogan, C. Couchoud, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Setting reasonable objectives for improving preemptive kidney transplantation rates in children

J. Bacchetta, J. Hogan, C. Couchoud, 2020, Pediatric Nephrology.

The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

G. Capasso, G. Remuzzi, J. Wetzels, 2021, Orphanet Journal of Rare Diseases.

Chronic kidney disease consecutive to chemotherapy for chondroblastic osteosarcoma: A report on 6 pediatric cases.

J. Bacchetta, P. Marec-Berard, L. Dubourg, 2021, Nephrologie & therapeutique.

Serum sclerostin: the missing link in the bone-vessel cross-talk in hemodialysis patients?

G. London, J. Bacchetta, M. Laville, 2015, Osteoporosis International.

[Pediatric nephrology in developing countries].

J. Bacchetta, P. Cochat, C. Mourani, 2009, Medecine tropicale : revue du Corps de sante colonial.

Eculizumab and thrombotic microangiopathy after hematopoietic stem cell transplantation: A report on its efficacy and safety in two pediatric patients.

J. Bacchetta, Y. Bertrand, E. Javouhey, 2018, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Mesothelioma of the testis and nephrotic syndrome: a case report

J. Bacchetta, J. Droz, F. Dijoud, 2009, Journal of medical case reports.

Are plasma proteins a valid alternative for assessing nephrotic syndrome in children from low-income countries?

J. Bacchetta, B. Ranchin, R. Cartier, 2022, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

To biopsy or not to biopsy: Henoch-Schönlein nephritis in children, a 5-year follow-up study

R. Salomon, J. Bacchetta, J. Hogan, 2021, Pediatric Nephrology.

Acute tubulointerstitial nephritis with or without uveitis: a novel form of post-acute COVID-19 syndrome in children

J. Casanova, J. Bacchetta, B. Ranchin, 2023, medRxiv.

2014 update of recommendations on the prevention and treatment of glucocorticoid-induced osteoporosis.

E. Lespessailles, J. Bacchetta, C. Roux, 2014, Joint, bone, spine : revue du rhumatisme.

[Renal abnormalities in Down syndrome: A review].

J. Bacchetta, B. Ranchin, D. Sanlaville, 2017, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Long-term steroid therapy in children: is adjunct therapy relevant in nephrotic syndrome?].

J. Bacchetta, P. Cochat, J. Harambat, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Sensenbrenner syndrome: a further challenge in evaluating sagittal synostosis and a need for a multidisciplinary approach

J. Bacchetta, F. Di Rocco, M. Rossi, 2021, Child's Nervous System.

Mouse Models of Mineral Bone Disorders Associated with Chronic Kidney Disease

J. Bacchetta, G. Laverny, C. Schmitt, 2023, International journal of molecular sciences.

Hydration and Nephrolithiasis in Pediatric Populations: Specificities and Current Recommendations

J. Bacchetta, A. Bertholet-Thomas, V. Bidault, 2023, Nutrients.

Hypertension in Children and Adolescents: A Position Statement From a Panel of Multidisciplinary Experts Coordinated by the French Society of Hypertension

J. Bacchetta, B. Ranchin, J. Fauvel, 2021, Frontiers in Pediatrics.

Impact of Cinacalcet and Etelcalcetide on Bone Mineral and Cardiovascular Disease in Dialysis Patients

J. Bacchetta, C. Schmitt, Aurélie De Mul, 2023, Current Osteoporosis Reports.

Klinefelter Bone Microarchitecture Evolution with Testosterone Replacement Therapy

J. Bacchetta, R. Chapurlat, P. Szulc, 2022, Calcified Tissue International.

Hypersensitivity to inulin: a rare and mostly benign event.

J. Bacchetta, P. Cochat, B. Kassaï, 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Escherichia coli-associated hemolytic uremic syndrome and severe chronic hepatocellular cholestasis: complication or side effect of eculizumab?

J. Bacchetta, E. Javouhey, S. Collardeau-Frachon, 2019, Pediatric nephrology (Berlin, West).

[Blueberry Muffin Baby and spontaneous remission of neonatal leukaemia].

J. Bacchetta, Y. Bertrand, M. Pagès, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Cardiac involvement in pediatric hemolytic uremic syndrome

J. Bacchetta, E. Javouhey, J. Rambaud, 2022, Pediatric Nephrology.

[Comparison of methods estimating a quantitative parameter: evaluation of the agreement].

J. Bacchetta, L. Juillard, N. Rognant, 2013, Néphrologie & Thérapeutique.

Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population.

K. Busiah, J. Salles, J. Bacchetta, 2020, European journal of endocrinology.

Nephrocalcinosis in very low birth weight infants: incidence, associated factors, and natural course

J. Bacchetta, P. Pradat, J. Picaud, 2022, Pediatric Nephrology.

Reloxaliase in Enteric Hyperoxaluria — The Recent Brake

J. Bacchetta, S. Lemoine, 2022, NEJM Evidence.

Assessment of Bone Microarchitecture in Chronic Kidney Disease: A Comparison of 2D Bone Texture Analysis and High-Resolution Peripheral Quantitative Computed Tomography at the Radius and Tibia

P. Delmas, E. Lespessailles, J. Bacchetta, 2010, Calcified Tissue International.

Bone microarchitecture is more severely affected in patients on hemodialysis than in those receiving peritoneal dialysis.

J. Bacchetta, D. Fouque, R. Chapurlat, 2012, Kidney international.

[What about the long-term renal outcome of premature babies?].

J. Bacchetta, P. Cochat, 2008, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

What is the best alternative to inulin clearance to estimate GFR in patients with decompensated alcoholic cirrhosis?

J. Dumortier, J. Bacchetta, L. Dubourg, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Erratum: Early impairment of trabecular microarchitecture assessed with HR‐pQCT in patients with stage II‐IV chronic kidney disease

P. Delmas, J. Bacchetta, L. Juillard, 2012 .

Biphasic Effects of Vitamin D and FGF23 on Human Osteoclast Biology

J. Bacchetta, P. Jurdic, I. Machuca‐Gayet, 2015, Calcified Tissue International.

GFR estimation in adolescents and young adults.

J. Bacchetta, B. Ranchin, P. Cochat, 2012, Journal of the American Society of Nephrology : JASN.

Severe neonatal hypercalcemia revealing congenital mesoblastic nephroma: A case report and management of neonatal hypercalcemia

J. Bacchetta, J. Pracros, C. Tanné, 2022, Archives de Pédiatrie.

Value of the RIFLE classification for acute kidney injury in diffuse proliferative lupus nephritis

J. Bacchetta, J. Drai, L. Juillard, 2009 .

Daily practice evaluation of the paediatric set of a next-generation long-term haemodialysis machine

J. Bacchetta, B. Ranchin, Aurélie De Mul, 2023, Pediatric nephrology.

Louisa Bloudeau1 · Agnès Linglart2 · Sacha Flammier1 · Aurélie Portefaix3 · Aurélia Bertholet‐Thomas1 · Sanaa Eddiry4 · Anna Barosi2 · Jean‐Pierre Salles4 · Valérie Porquet‐Bordes4 · Anya Rothenbuhler2 · Christelle Roger5,6 · Justine Bacchetta1,6,7,8

J. Salles, J. Bacchetta, A. Rothenbuhler, 2022 .

Clinical Factors and Adverse Kidney Outcomes in Children With ANCA-Associated Glomerulonephritis.

M. Marlais, M. Szczepańska, J. Bacchetta, 2022, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Longitudinal Bone Mineralization Assessment in Children Treated With Long‐Term Parenteral Nutrition for Severe Intestinal Failure

J. Bacchetta, N. Peretti, P. Braillon, 2017, JPEN. Journal of parenteral and enteral nutrition.

Eculizumab in neonatal hemolytic uremic syndrome with homozygous factor H deficiency

J. Bacchetta, E. Javouhey, P. Cochat, 2014, Pediatric Nephrology.

Evolution of renal oxygen content measured by BOLD MRI downstream a chronic renal artery stenosis.

M. Janier, J. Bacchetta, R. Gadet, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Iconography : 2014 update of recommendations on the prevention and treatment of glucocorticoid-induced osteoporosis

E. Lespessailles, J. Bacchetta, C. Roux, 2015 .

Fludrocortisone as a new tool for managing tubulopathy after pediatric renal transplantation: a series of cases

J. Bacchetta, B. Ranchin, P. Cochat, 2014, Pediatric Nephrology.

IVIg therapy in the management of BK virus infections in pediatric kidney transplant patients.

J. Bacchetta, B. Ranchin, Y. Mekki, 2023, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Young XLH Patients-Reported Experience with a Supportive Care Program

J. Bacchetta, C. Audrain, S. Rossignol, 2023, Patient preference and adherence.

Genetic assessment in primary hyperoxaluria: why it matters

J. Bacchetta, J. Groothoff, G. Mandrile, 2022, Pediatric Nephrology.

Isolated kidney transplantation under lumasiran therapy in primary hyperoxaluria type 1: a report of 5 cases.

J. Bacchetta, J. Groothoff, B. Moulin, 2022, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Calcium balance in pediatric online hemodiafiltration: Beware of sodium and bicarbonate in the dialysate.

J. Bacchetta, B. Ranchin, R. Cartier, 2015, Nephrologie & therapeutique.

Pediatric atypical hemolytic–uremic syndrome due to auto-antibodies against factor H: is there an interest to combine eculizumab and mycophenolate mofetil?

J. Bacchetta, B. Ranchin, A. Sellier-Leclerc, 2021, Pediatric Nephrology.

Autoimmune hypoparathyroidism in a 12-year-old girl with McKusick cartilage hair hypoplasia

J. Bacchetta, B. Ranchin, R. Bouvier, 2009, Pediatric Nephrology.

Skin microvascular dysfunction as an early cardiovascular marker in primary hyperoxaluria type I

J. Bacchetta, B. Fromy, P. Cochat, 2018, Pediatric Nephrology.

[Online hemodiafiltration in children and hypoparathyroidism: a single-centre series of cases].

J. Bacchetta, B. Ranchin, A. Belot, 2014, Nephrologie & therapeutique.

Erratum: Osteocalcin Signaling in Myofibers Is Necessary and Sufficient for Optimum Adaptation to Exercise (Cell Metabolism (2016) 23(6) (1078–1092)(S1550413116302224)(10.1016/j.cmet.2016.05.004))

R. Cabo, R. Kitsis, R. Friedman, 2017 .