M. Tête

发表

Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.

O. Gribouval, C. Antignac, G. Benoît, 2010, Journal of the American Society of Nephrology : JASN.

APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.

O. Gribouval, C. Antignac, B. Knebelmann, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Varicella and zoster in children after kidney transplantation: long-term results of vaccination.

C. Rouzioux, G. Guest, M. Broyer, 1997, Pediatrics.

Insulin and growth hormone secretion in dialyzed children: influence of dietary manipulation.

P. Czernichow, M. Laudat, M. Broyer, 1978, The American journal of clinical nutrition.

Diabetes mellitus in patients with infantile cystinosis after renal transplantation

P. Niaudet, J. Robert, G. Guest, 1999, Pediatric Nephrology.

Plasma lipids, lipoproteins and apolipoproteins AI, AII, and B in renal transplanted children: what risk for accelerated atherosclerosis?

M. Laudat, S. Goldstein, M. Broyer, 1984, Nephron.

Late symptoms in infantile cystinosis

M. Gubler, M. Broyer, M. Tête, 1987, Pediatric Nephrology.

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

O. Gribouval, C. Antignac, P. Niaudet, 2004, Kidney international.

Plasma lipids in kidney transplanted children and adolescents: influence of pubertal development, dietary intake and steroid therapy

M. Laudat, M. Broyer, M. Tête, 1981, European journal of clinical investigation.

Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults.

O. Gribouval, C. Antignac, D. Chauveau, 2018, Kidney international.

Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults.

C. Antignac, P. Niaudet, A. Servais, 2012, Kidney international.

Clinical polymorphism of cystinosis encephalopathy. Results of treatment with cysteamine

F. Labrousse, G. Guest, M. Broyer, 1996, Journal of Inherited Metabolic Disease.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

A. Köttgen, T. Ahluwalia, O. Gribouval, 2019, The Journal of clinical investigation.

Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.

T. Benzing, O. Gribouval, C. Antignac, 2008, Journal of the American Society of Nephrology : JASN.

LMX1B mutations cause hereditary FSGS without extrarenal involvement.

J. Szustakowski, B. Linghu, E. Oakeley, 2013, Journal of the American Society of Nephrology : JASN.

Treatment of severe childhood nephrosis.

P. Niaudet, M. Broyer, R. Habib, 1988, Advances in nephrology from the Necker Hospital.

Cyclosporin in the treatment of idiopathic nephrotic syndrome in children

P. Niaudet, M. Broyer, R. Habib, 1987, Pediatric Nephrology.

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

K. Dahan, R. Salomon, O. Gribouval, 2018, Pediatric Nephrology.

Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.

G. Mollet, O. Gribouval, C. Antignac, 2011, Journal of the American Society of Nephrology : JASN.

LONG-TERM SOCIAL OUTCOME OF CHILDREN AFTER KIDNEY TRANSPLANTATION

P. Niaudet, M. Charbit, G. Guest, 2004, Transplantation.

Loss of graft by chronic rejection in a series of pediatric kidney transplantation: predictive value of biopsy.

D. Droz, P. Niaudet, M. Charbit, 1998, Transplantation proceedings.

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.

G. Mollet, O. Gribouval, C. Antignac, 2011, The New England journal of medicine.

Cyclosporine and childhood idiopathic nephrosis.

P. Niaudet, M. Broyer, R. Habib, 1988, Transplantation proceedings.

Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy

J. Robert, M. le Merrer, P. Castelnau, 2000, European Journal of Pediatrics.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

A. Köttgen, T. Ahluwalia, O. Gribouval, 2019, The Journal of clinical investigation.