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Lithium nephrotoxicity revisited

Nature reviews. Nephrology, 2009-05, Vol.5 (5), p.270-276

2009

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Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

Journal of medical genetics, 2007-03, Vol.44 (3), p.193-199

2007

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Increased risk of solid renal tumors in lithium-treated patients

Kidney international, 2014-07, Vol.86 (1), p.184-190

2014

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Cyst Infections in Patients with Autosomal Dominant Polycystic Kidney Disease

Clinical journal of the American Society of Nephrology, 2009-07, Vol.4 (7), p.1183-1189

2009

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Screening for intracranial aneurysms in autosomal dominant polycystic kidney disease is cost-effective

Kidney international, 2018-03, Vol.93 (3), p.716-726

2018

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Axel, un amoureux des mots et de la Science

M.S. Médecine sciences, 2021-12, Vol.37, p.11-11

Grünfeld, Jean-Pierre

2021

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Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Kidney international, 2012-08, Vol.82 (4), p.454-464

2012

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Urinary Procollagen III Aminoterminal Propeptide (PIIINP): A Fibrotest for the Nephrologist

Clinical journal of the American Society of Nephrology, 2010-02, Vol.5 (2), p.205-210

2010

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Longer duration of predialysis nephrological care is associated with improved long‐term survival of dialysis patients

Nephrology, dialysis, transplantation, 2001-12, Vol.16 (12), p.2357-2364

2001

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Nonprogressive Kidney Dysfunction and Outcomes in Older Adults with Chronic Kidney Disease

Journal of the American Geriatrics Society (JAGS), 2009-12, Vol.57 (12), p.2217-2223

2009

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Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Nature genetics, 1997-12, Vol.17 (4), p.467-470

1997

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Renal Involvement in Cystic Fibrosis: Diseases Spectrum and Clinical Relevance

Clinical journal of the American Society of Nephrology, 2009-05, Vol.4 (5), p.921-928

2009

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Rare inherited disorders with renal involvement—approach to the patient

Kidney international, 2015-05, Vol.87 (5), p.901-908

2015

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Screening and management of intracranial aneurisms in patients with autosomal dominant polycystic kidney disease

Néphrologie & thérapeutique, 2017-04, Vol.13 Suppl 1, p.S147-S153

2017

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Autosomal recessive polycystic kidney disease in adulthood

Nephrology, dialysis, transplantation, 2001-08, Vol.16 (8), p.1648-1652

2001

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Comparison between siblings and twins supports a role for modifier genes in ADPKD

Kidney international, 2004-12, Vol.66 (6), p.2132-2136

2004

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Renal and thymic pathology in thymoma-associated nephropathy: report of 21 cases and review of the literature

Nephrology, dialysis, transplantation, 2005-06, Vol.20 (6), p.1075-1082

2005

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Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant

Kidney international, 2009-04, Vol.75 (7), p.727-735

2009

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A large subset of neutrophils expressing membrane proteinase 3 is a risk factor for vasculitis and rheumatoid arthritis

Journal of the American Society of Nephrology, 1999-06, Vol.10 (6), p.1224-1233

1999

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Rituximab prevents recurrence of thrombotic thrombocytopenic purpura: a case report

Blood, 2005-08, Vol.106 (3), p.925-928

2005

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Cyclosporin therapy in patients with Alport syndrome

Pediatric nephrology (Berlin, West), 2007-01, Vol.22 (1), p.57-63

2007

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Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy

Kidney international, 2012-03, Vol.81 (5), p.494-501

2012

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Genotype–phenotype correlation in von Hippel‐Lindau families with renal lesions

Human mutation, 2004-09, Vol.24 (3), p.215-224

2004

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3-Nitrotyrosine as a biomarker for vascular involvement in Fabry disease

Kidney international, 2014-07, Vol.86 (1), p.5-7

2014

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Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

Kidney international, 2012-04, Vol.81 (8), p.779-783

2012

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Lithium nephrotoxicity revisited

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

Increased risk of solid renal tumors in lithium-treated patients

Cyst Infections in Patients with Autosomal Dominant Polycystic Kidney Disease

Screening for intracranial aneurysms in autosomal dominant polycystic kidney disease is cost-effective

Axel, un amoureux des mots et de la Science

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

Urinary Procollagen III Aminoterminal Propeptide (PIIINP): A Fibrotest for the Nephrologist

Longer duration of predialysis nephrological care is associated with improved long‐term survival of dialysis patients

Nonprogressive Kidney Dysfunction and Outcomes in Older Adults with Chronic Kidney Disease

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Renal Involvement in Cystic Fibrosis: Diseases Spectrum and Clinical Relevance

Rare inherited disorders with renal involvement—approach to the patient

Screening and management of intracranial aneurisms in patients with autosomal dominant polycystic kidney disease

Autosomal recessive polycystic kidney disease in adulthood

Comparison between siblings and twins supports a role for modifier genes in ADPKD

Renal and thymic pathology in thymoma-associated nephropathy: report of 21 cases and review of the literature

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant

A large subset of neutrophils expressing membrane proteinase 3 is a risk factor for vasculitis and rheumatoid arthritis

Rituximab prevents recurrence of thrombotic thrombocytopenic purpura: a case report

Cyclosporin therapy in patients with Alport syndrome

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy

Genotype–phenotype correlation in von Hippel‐Lindau families with renal lesions

3-Nitrotyrosine as a biomarker for vascular involvement in Fabry disease

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutations

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