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Cystinuria: an update on pathophysiology, genetics, and clinical management

Pediatric nephrology (Berlin, West), 2022-08, Vol.37 (8), p.1705-1711

2022

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Unravelling the Complex Relationship between Diet and Nephrolithiasis: The Role of Nutrigenomics and Nutrigenetics

Nutrients, 2022-11, Vol.14 (23), p.4961

2022

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Lumasiran in the Management of Patients with Primary Hyperoxaluria Type 1: From Bench to Bedside

International journal of nephrology and renovascular disease, 2022-06, Vol.15, p.197-206

2022

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Kidney involvement in hereditary transthyretin amyloidosis: is there a role for cystatin C?

Clinical kidney journal, 2023-02, Vol.16 (2), p.397-398

2023

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Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and Nephrolithiasis

Kidney & blood pressure research, 2021-08, Vol.46 (4), p.469-474

2021

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Renal Involvement in Hereditary Transthyretin Amyloidosis: An Italian Single-Centre Experience

Brain sciences, 2021-07, Vol.11 (8), p.980

2021

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Trajectories of Kidney Function in Patients with ATTRv Treated with Gene Silencers

Genes, 2022-11, Vol.13 (12), p.2236

2022

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Why is diagnosis, investigation, and improved management of kidney stone disease important? Non-pharmacological and pharmacological treatments for nephrolithiasis

Expert review of clinical pharmacology, 2022-04, Vol.15 (4), p.407-414

2022

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Complications and Treatment of Hypercalciuria in Familial Hyperkalae-mic Hypertension (FHHt): FR-OR45

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.30-30

2022

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MO060CYSTINURIA: DISEASE PRESENTATION, PROGNOSIS AND QUALITY OF LIFE ANALYSIS OF A WEB-BASED COHORT

Nephrology, dialysis, transplantation, 2021-05, Vol.36 (Supplement_1)

2021

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1333 SGLT2 inhibitors as a treatment for Fanconi-Bickel syndrome: a case report

Nephrology, dialysis, transplantation, 2024-05, Vol.39 (Supplement_1)

2024

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1905 Sex differences in primary distal renal tubular acidosis: a single-centre retrospective study

Nephrology, dialysis, transplantation, 2024-05, Vol.39 (Supplement_1)

2024

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A clinical screening algorithm for primary hyperoxaluria type 1 in adults on dialysis

Nephrology, dialysis, transplantation, 2024-01, Vol.39 (2), p.367-370

2024

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174 Valvulopathies and left ventricular hypertrophy in ADPKD: prevalence and association with genotype and phenotype

Nephrology, dialysis, transplantation, 2024-05, Vol.39 (Supplement_1)

2024

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MO038: Mineral bone density assessment in patients affected by cystinuria

Nephrology, dialysis, transplantation, 2022-05, Vol.37 (Supplement_3)

2022

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MO487: Rates of Hyperkal a EMIA and Management Patterns in a Tertiary Outpatient Renal Clinic

Nephrology, dialysis, transplantation, 2022-05, Vol.37 (Supplement_3)

2022

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P0058THE ROLE OF GENETICS IN INCOMPLETE DISTAL RENAL TUBULAR ACIDOSIS IN NEPHROLITHIASIS

Nephrology, dialysis, transplantation, 2020-06, Vol.35 (Supplement_3)

2020

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MO852MANAGEMENT OF PATIENTS UNDERGOING CHRONIC HEMODIALYSIS DURING THE COVID-19 PANDEMIC: FONDAZIONE POLICLINICO A. GEMELLI’S EXPERIENCE

Nephrology, dialysis, transplantation, 2021-05, Vol.36 (Supplement_1)

2021

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MO852MANAGEMENT OF PATIENTS UNDERGOING CHRONIC HEMODIALYSIS DURING THE COVID-19 PANDEMIC: FONDAZIONE POLICLINICO A. GEMELLI’S EXPERIENCE

Nephrology, dialysis, transplantation, 2021-05, Vol.36 (Suppl 1)

2021

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Hyperoxaluric acute kidney injury and frontotemporal dementia

The Lancet (British edition), 2023-05, Vol.401 (10387), p.1530-1530

2023

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A female patient with Dent disease due to skewed X-chromosome inactivation

Clinical kidney journal, 2024-06, Vol.17 (6), p.sfae092

2024

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α-lipoic acid in patients with autosomal dominant polycystic kidney disease

Nutrition (Burbank, Los Angeles County, Calif.), 2020-03, Vol.71, p.110594-110594, Article 110594

2020

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Bone mineral density assessment in patients with cystinuria

Journal of nephrology, 2024-07

2024

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Management of the kidney transplant patient with Cancer: Report from a Multidisciplinary Consensus Conference

Transplantation reviews (Philadelphia, Pa.), 2021-07, Vol.35 (3), p.100636-100636, Article 100636

2021

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Cystinuria: an update on pathophysiology, genetics, and clinical management

Unravelling the Complex Relationship between Diet and Nephrolithiasis: The Role of Nutrigenomics and Nutrigenetics

Lumasiran in the Management of Patients with Primary Hyperoxaluria Type 1: From Bench to Bedside

Kidney involvement in hereditary transthyretin amyloidosis: is there a role for cystatin C?

Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and Nephrolithiasis

Renal Involvement in Hereditary Transthyretin Amyloidosis: An Italian Single-Centre Experience

Trajectories of Kidney Function in Patients with ATTRv Treated with Gene Silencers

Why is diagnosis, investigation, and improved management of kidney stone disease important? Non-pharmacological and pharmacological treatments for nephrolithiasis

Complications and Treatment of Hypercalciuria in Familial Hyperkalae-mic Hypertension (FHHt): FR-OR45

MO060CYSTINURIA: DISEASE PRESENTATION, PROGNOSIS AND QUALITY OF LIFE ANALYSIS OF A WEB-BASED COHORT

1333 SGLT2 inhibitors as a treatment for Fanconi-Bickel syndrome: a case report

1905 Sex differences in primary distal renal tubular acidosis: a single-centre retrospective study

A clinical screening algorithm for primary hyperoxaluria type 1 in adults on dialysis

174 Valvulopathies and left ventricular hypertrophy in ADPKD: prevalence and association with genotype and phenotype

MO038: Mineral bone density assessment in patients affected by cystinuria

MO487: Rates of Hyperkal a EMIA and Management Patterns in a Tertiary Outpatient Renal Clinic

P0058THE ROLE OF GENETICS IN INCOMPLETE DISTAL RENAL TUBULAR ACIDOSIS IN NEPHROLITHIASIS

MO852MANAGEMENT OF PATIENTS UNDERGOING CHRONIC HEMODIALYSIS DURING THE COVID-19 PANDEMIC: FONDAZIONE POLICLINICO A. GEMELLI’S EXPERIENCE

MO852MANAGEMENT OF PATIENTS UNDERGOING CHRONIC HEMODIALYSIS DURING THE COVID-19 PANDEMIC: FONDAZIONE POLICLINICO A. GEMELLI’S EXPERIENCE

Hyperoxaluric acute kidney injury and frontotemporal dementia

A female patient with Dent disease due to skewed X-chromosome inactivation

α-lipoic acid in patients with autosomal dominant polycystic kidney disease

Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium

Bone mineral density assessment in patients with cystinuria

Management of the kidney transplant patient with Cancer: Report from a Multidisciplinary Consensus Conference

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