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Increase of circulating neutrophil and platelet microparticles during acute vasculitis and hemodialysis

Kidney international, 2006-04, Vol.69 (8), p.1416-1423

2006

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Prevention of cardiovascular events in end-stage renal disease: Results of a randomized trial of fosinopril and implications for future studies

Kidney international, 2006-10, Vol.70 (7), p.1318-1324

2006

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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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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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Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN)

Nephrology, dialysis, transplantation, 2010-07, Vol.25 (7), p.2168-2177

2010

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Determination of the Genomic Structure of the COL4A4 Gene and of Novel Mutations Causing Autosomal Recessive Alport Syndrome

American journal of human genetics, 1998-11, Vol.63 (5), p.1329-1340

1998

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Maladie de Fabry et cystinose, deux maladies lysosomales : similitudes et différences

La Revue de médecine interne (Paris), 2010-12, Vol.31, p.S226-S228

2010

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Non-invasive evaluation of arterial involvement in patients affected with Fabry disease

Journal of medical genetics, 2001-09, Vol.38 (9), p.629-631

2001

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Familial amyloid polyneuropathy type I (Portuguese): Distribution and characterization of renal amyloid deposits

American journal of kidney diseases, 1998-06, Vol.31 (6), p.940-946

1998

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Gitelman syndrome comes of age

Nephrology, dialysis, transplantation, 1998-07, Vol.13 (7), p.1617-1619

1998

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Insuffisance rénale chronique sous lithium: Démarche pluridisciplinaire du néphrologue, du psychiatre et…du patient

Encéphale, 2008, Vol.34 (4), p.440-441

2008

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Clinical outcome following coronary angioplasty in dialysis patients: a case–control study in the era of coronary stenting

British heart journal, 2001-05, Vol.85 (5), p.556-560

2001

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The intrarenal vascular lesions associated with primary antiphospholipid syndrome

Journal of the American Society of Nephrology, 1999-03, Vol.10 (3), p.507-518

1999

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Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness

Journal of medical genetics, 1995-08, Vol.32 (8), p.654-656

1995

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Pregnancy in von Hippel-Lindau disease

American journal of obstetrics and gynecology, 1999, Vol.180 (1), p.110-111

1999

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Glucocorticoids Modulate Vascular Reactivity in the Rat

Hypertension (Dallas, Tex. 1979), 1987-12, Vol.10 (6), p.608-618

1987

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Randomised controlled trial of enalapril and beta blockers in non-diabetic chronic renal failure

BMJ (Online), 1994-10, Vol.309 (6958), p.833

1994

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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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Renal disease in Fabry patients

Journal of inherited metabolic disease, 2001-01, Vol.24 (S2), p.71-74

2001

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Factors influencing progression of renal failure in autosomal dominant polycystic kidney disease

American journal of kidney diseases, 1998-11, Vol.32 (5), p.xlvi-xlviii

Grünfeld, J P

1998

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CONTEMPORARY DIAGNOSTIC APPROACH IN ALPORT'S SYNDROME

Renal failure, 2000-01, Vol.22 (6), p.759-763

Grünfeld, Jean-Pierre

2000

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Deletions in the COL4A5 collagen gene in X-linked Alport syndrome : characterization of the pathological transcripts in nonrenal cells and correlation with disease expression

The Journal of clinical investigation, 1994-03, Vol.93 (3), p.1195-1207

1994

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The clinical spectrum of hereditary nephritis

Kidney international, 1985-01, Vol.27 (1), p.83-92

GRUNFELD, J.-P

1985

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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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AL amyloidosis and monoclonal immunoglobulin deposit diseases

La revue de medecine interne, 2001-06, Vol.22 Suppl 1, p.16s-17s

2001

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Increase of circulating neutrophil and platelet microparticles during acute vasculitis and hemodialysis

Prevention of cardiovascular events in end-stage renal disease: Results of a randomized trial of fosinopril and implications for future studies

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

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

Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN)

Determination of the Genomic Structure of the COL4A4 Gene and of Novel Mutations Causing Autosomal Recessive Alport Syndrome

Maladie de Fabry et cystinose, deux maladies lysosomales : similitudes et différences

Non-invasive evaluation of arterial involvement in patients affected with Fabry disease

Familial amyloid polyneuropathy type I (Portuguese): Distribution and characterization of renal amyloid deposits

Gitelman syndrome comes of age

Insuffisance rénale chronique sous lithium: Démarche pluridisciplinaire du néphrologue, du psychiatre et…du patient

Clinical outcome following coronary angioplasty in dialysis patients: a case–control study in the era of coronary stenting

The intrarenal vascular lesions associated with primary antiphospholipid syndrome

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness

Pregnancy in von Hippel-Lindau disease

Glucocorticoids Modulate Vascular Reactivity in the Rat

Randomised controlled trial of enalapril and beta blockers in non-diabetic chronic renal failure

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

Renal disease in Fabry patients

Factors influencing progression of renal failure in autosomal dominant polycystic kidney disease

CONTEMPORARY DIAGNOSTIC APPROACH IN ALPORT'S SYNDROME

Deletions in the COL4A5 collagen gene in X-linked Alport syndrome : characterization of the pathological transcripts in nonrenal cells and correlation with disease expression

The clinical spectrum of hereditary nephritis

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

AL amyloidosis and monoclonal immunoglobulin deposit diseases

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