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Author Details
Full Name
Francesco Emma
Affiliation
Ospedale Pediatrico Bambino Gesu IRCCS
ORCID
Career Start Year
1983
Papers
210
H Index
49
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37466865
A child with semaphorin 3b-associated membranous nephropathy effectively treated with obinutuzumab after rituximab resistance.
Pediatr Nephrol
2024
36300303
Genistein improves renal disease in a mouse model of nephropathic cystinosis: a comparison study with cysteamine.
Hum Mol Genet
2023
37561590
A phase I study of autologous mesenchymal stromal cells for severe steroid-dependent nephrotic syndrome.
JCI Insight
2023
37385541
Age and memory B cells at baseline are associated with risk of relapse and memory B-cell reappearance following anti-CD20 treatment in pediatric frequently-relapsing/steroid-dependent nephrotic syndrome.
Kidney Int
2023
37041389
A pediatric case of IgA nephropathy benefitting from targeted release formulation-budesonide.
Pediatr Nephrol
2023
37306717
Successful treatment with avacopan (CCX168) in a pediatric patient with C3 glomerulonephritis.
Pediatr Nephrol
2023
36434353
Treatment of idiopathic nephrotic syndrome at onset: a comparison between 8- and 12-week regimens in everyday clinical practice.
Pediatr Nephrol
2023
36315273
Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression.
Pediatr Nephrol
2023
34661744
Circulating plasmablasts in children with steroid-sensitive nephrotic syndrome.
Pediatr Nephrol
2022
35643375
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Kidney Int
2022
35483523
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Kidney Int
2022
35681534
Biomarkers in Nephropathic Cystinosis: Current and Future Perspectives.
Cells
2022
36344218
How I Treat Steroid-Sensitive Nephrotic Syndrome in Children.
Clin J Am Soc Nephrol
2022
36082134
Post-authorisation safety study of burosumab use in paediatric, adolescent and adult patients with X-linked hypophosphataemia: rationale and description.
Ther Adv Chronic Dis
2022
36003666
Expert guidance on the multidisciplinary management of cystinosis in adolescent and adult patients.
Clin Kidney J
2022
33665752
Update on the treatment of steroid-sensitive nephrotic syndrome.
Pediatr Nephrol
2022
35218550
Primary hyperoxaluria in Italy: the past 30Â years and the near future of a (not so) rare disease.
J Nephrol
2022
35137195
Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.
Nephrol Dial Transplant
2022
35137071
Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosis.
Hum Mol Genet
2022
34383126
Belimumab for the treatment of children with frequently relapsing nephrotic syndrome: the BELNEPH study.
Pediatr Nephrol
2022
32840097
Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
J Clin Res Pediatr Endocrinol
2021
33770395
Distal renal tubular acidosis: a systematic approach from diagnosis to treatment.
J Nephrol
2021
33509356
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders.
Kidney Int
2021
33776994
Evaluation of Immune and Vaccine Competence in Steroid-Sensitive Nephrotic Syndrome Pediatric Patients.
Front Immunol
2021
33914889
Distal renal tubular acidosis: ERKNet/ESPN clinical practice points.
Nephrol Dial Transplant
2021
34943802
Benefits and Toxicity of Disulfiram in Preclinical Models of Nephropathic Cystinosis.
Cells
2021
34884638
Drug Repurposing in Rare Diseases: An Integrative Study of Drug Screening and Transcriptomic Analysis in Nephropathic Cystinosis.
Int J Mol Sci
2021
34544820
Human or Chimeric Monoclonal Anti-CD20 Antibodies for Children with Nephrotic Syndrome: A Superiority Randomized Trial.
J Am Soc Nephrol
2021
34845071
Randomised controlled trial comparing rituximab to mycophenolate mofetil in children and young adults with steroid-dependent idiopathic nephrotic syndrome: study protocol.
BMJ Open
2021
34078418
The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results.
Orphanet J Rare Dis
2021
34294211
Corrigendum to Flemming J, Marczenke M, Rudolph I-M, et al. Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome. Kidney Int. 2020;98:159-167.
Kidney Int
2021
34237326
An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis.
Kidney Int
2021
34049919
Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients: a cross-sectional web-based survey.
BMJ Open
2021
33025206
IgM on the surface of T cells: a novel biomarker of pediatric-onset systemic lupus erythematosus.
Pediatr Nephrol
2021
33152448
Results of the PROPINE randomized controlled study suggest tapering of prednisone treatment for relapses of steroid sensitive nephrotic syndrome is not necessary in children.
Kidney Int
2021
32918941
Cystinuria: clinical practice recommendation.
Kidney Int
2021
30418652
Is there long-term value of pathology scoring in immunoglobulin A nephropathy? A validation study of the Oxford Classification for IgA Nephropathy (VALIGA) update.
Nephrol Dial Transplant
2020
33615080
Efficacy of Eculizumab in Coexisting Complement C3 Glomerulopathy and Atypical Hemolytic Uremic Syndrome.
Kidney Int Rep
2020
31667616
Ofatumumab rescue treatment in post-transplant recurrence of focal segmental glomerulosclerosis.
Pediatr Nephrol
2020
31959358
Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis.
Kidney Int
2020
33103447
Beyond the tubule: pathological variants of <i>LRP2</i>, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease.
Am J Physiol Renal Physiol
2020
32503896
Cell-Based Phenotypic Drug Screening Identifies Luteolin as Candidate Therapeutic for Nephropathic Cystinosis.
J Am Soc Nephrol
2020
32471643
Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome.
Kidney Int
2020
32534052
Semaphorin 3B-associated membranous nephropathy is a distinct type of disease predominantly present in pediatric patients.
Kidney Int
2020
31550240
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.
J Clin Invest
2020
30403813
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome.
Nephrol Dial Transplant
2020
30418563
Renal Tubular Dysfunction Fully Accounts for Plasma Biochemical Abnormalities in Type 1A Pseudohypoparathyroidism.
J Clin Endocrinol Metab
2019
31759484
A new mouse model of anti-GBM disease sheds light on maternal transfer of alloantibodies in glomerular disease.
Kidney Int
2019
31888107
Mitochondrial Dynamics of Proximal Tubular Epithelial Cells in Nephropathic Cystinosis.
Int J Mol Sci
2019
31709256
NLRP2 Regulates Proinflammatory and Antiapoptotic Responses in Proximal Tubular Epithelial Cells.
Front Cell Dev Biol
2019
1 - 50 of 210
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row(s) 1 - 30 of 30
Collaborators
Franz Schaefer
University Children's Hospital Heidelberg
Co-authored papers
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Enrico Bertini
IRCCS Bambino Gesu Children's Research Hospital
Co-authored papers
13
Olivier Devuyst
Institute of Physiology, University of Zurich, Cliniques Universitaires Saint-Luc
Co-authored papers
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Detlef Bockenhauer
Great Ormond Street Hospital for Children, NHS Foundation Trust
Co-authored papers
8
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University of Pavia
Co-authored papers
6
Jun Oh
Konyang University Hospital
Co-authored papers
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Joseph G Gleeson
University of California
Co-authored papers
3
Friedhelm Hildebrandt
Boston Children's Hospital
Co-authored papers
3
Andrew M Herzenberg
University of Toronto
Co-authored papers
3
Eugen Boltshauser
Children's University Hospital
Co-authored papers
3
Stefano D'Arrigo
Fondazione IRCCS Istituto Neurologico Carlo Besta
Co-authored papers
3
Vivette D D'Agati
Columbia University Irving Medical Center
Co-authored papers
3
Bruno Dallapiccola
Co-authored papers
3
Jennifer L Silhavy
University of California
Co-authored papers
2
William A Gahl
National Human Genome Research Institute, National Institutes of Health
Co-authored papers
2
Giovanni Gambaro
Co-authored papers
2
Renato Borgatti
University of Pavia
Co-authored papers
2
Shrikant Mane
Yale School of Medicine
Co-authored papers
2
Romina Romaniello
IRCCS Mondino Foundation
Co-authored papers
2
Laura Barisoni
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