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Psychosocial quality of life in hereditary haemorrhagic telangiectasia patients

Rhinology, 2011-06, Vol.49 (2), p.164-167

2011

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Detection of polyglutamine expansion in a new acidic protein : a candidate for childhood onset schizophrenia?

Molecular psychiatry, 1999, Vol.4 (1), p.58-63

1999

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Mutations of NPHP2 and NPHP3 in infantile nephronophthisis

Kidney international, 2009-04, Vol.75 (8), p.839-847

2009

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

Kidney international, 2004-08, Vol.66 (2), p.571-579

2004

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Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults

Nephrology, dialysis, transplantation, 2006-09, Vol.21 (9), p.2660-2663

2006

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Molecular characterization of corona radiata cells from patients with diminished ovarian reserve using microarray and microfluidic-based gene expression profiling

Human reproduction (Oxford), 2012-03, Vol.27 (3), p.829-843

2012

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High NPHP1 and NPHP6 mutation rate in patients with joubert syndrome and nephronophthisis : Potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations

Journal of the American Society of Nephrology, 2007-05, Vol.18 (5), p.1566-1575

2007

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RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

Journal of medical genetics, 2011-07, Vol.48 (7), p.497-504

2011

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Is low plasma 25-(OH)vitamin D a major risk factor for hyperparathyroidism and Looser's zones independent of calcitriol?

Kidney international, 1999-06, Vol.55 (6), p.2169-2177

1999

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Epidermal Growth Factor Receptor Protein Detection in Head and Neck Cancer Patients: A Many-Faceted Picture

Clinical cancer research, 2012-03, Vol.18 (5), p.1313-1322

2012

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Prevalence of mutations in renal developmental genes in children with renal hypodysplasia : Results of the ESCAPE study

Journal of the American Society of Nephrology, 2006-10, Vol.17 (10), p.2864-2870

2006

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Bone mineral density directly correlates with elevated serum leptin in haemodialysis patients

Nephrology, dialysis, transplantation, 2003-09, Vol.18 (9), p.1882-1890

2003

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Maternal uniparental heterodisomy of chromosome 17 in a patient with nephropathic cystinosis

European journal of human genetics : EJHG, 2009-08, Vol.17 (8), p.1019-1023

2009

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Measuring cervical length with ultrasound: evaluation of the procedures and duration of a learning method

Ultrasound in obstetrics & gynecology, 2002-12, Vol.20 (6), p.575-579

2002

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Importance of vitamin D repletion in uraemia

Nephrology, dialysis, transplantation, 1999-04, Vol.14 (4), p.819-823

1999

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Spi-1 PU.1 but not Fli-1 inhibits erythroid-specific alternative splicing of 4.1R pre-mRNA in murine erythroleukemia cells

Oncogene, 2004-01, Vol.23 (4), p.920-927

2004

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Sevelamer hydrochloride with or without alphacalcidol or higher dialysate calcium vs calcium carbonate in dialysis patients: an open‐label, randomized study

Nephrology, dialysis, transplantation, 2003-03, Vol.18 (3), p.582-589

2003

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Protein 4.1R expression in normal and dystrophic skeletal muscle

Comptes rendus. Biologies, 2005, Vol.328 (1), p.43-56

2005

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Percutaneous recanalization of occlusion of central and proximal veins in chronic hemodialysis: Technical Note

Kidney international, 1997-11, Vol.52 (5), p.1406-1411

1997

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Magnesium Hydroxide as a Complementary Aluminium-free Phosphate Binder to Moderate Doses of Oral Calcium in Uraemic Patients on Chronic Haemodialysis: Lack of Deleterious Effect on Bone Mineralisation

Nephrology, dialysis, transplantation, 1988, Vol.3 (5), p.651-656

1988

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Reactivation of Optic Nerve Head Astrocytes by TGF-β2 and H2O2 Is Accompanied by Increased Hsp32 and Hsp47 Expression

Investigative ophthalmology & visual science, 2009-04, Vol.50 (4), p.1707-1717

2009

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Comparison of intact, midregion, and carboxy terminal assays of parathyroid hormone for the diagnosis of bone disease in hemodialyzed patients

The journal of clinical endocrinology and metabolism, 1991-09, Vol.73 (3), p.516-524

1991

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7-84 PTH or aluminum antagonism in the resistance of uremic bone to the remodeling effect of endogenous PTH? Author's reply

Kidney international, 2001, Vol.59 (6), p.2375-2376

2001

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Prevention of osteitis fibrosa, aluminium bone disease and soft-tissue calcification in dialysis patients: a long-term comparison of moderate doses of oral calcium±Mg(OH)2 vs Al(OH)3±1α OH vitamin D3

Nephrology, dialysis, transplantation, 1989, Vol.4 (12), p.1045-1053

1989

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Erosive osteoarthropathy associated with β2-microglobulin amyloidosis in a uraemic patient treated exclusively by long-term haemofiltration with biocompatible membranes

Nephrology, dialysis, transplantation, 1988, Vol.3 (6), p.820-822

1988

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Psychosocial quality of life in hereditary haemorrhagic telangiectasia patients

Detection of polyglutamine expansion in a new acidic protein : a candidate for childhood onset schizophrenia?

Mutations of NPHP2 and NPHP3 in infantile nephronophthisis

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

Nephronophthisis related to homozygous NPHP1 gene deletion as a cause of chronic renal failure in adults

Molecular characterization of corona radiata cells from patients with diminished ovarian reserve using microarray and microfluidic-based gene expression profiling

High NPHP1 and NPHP6 mutation rate in patients with joubert syndrome and nephronophthisis : Potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

Is low plasma 25-(OH)vitamin D a major risk factor for hyperparathyroidism and Looser's zones independent of calcitriol?

Epidermal Growth Factor Receptor Protein Detection in Head and Neck Cancer Patients: A Many-Faceted Picture

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia : Results of the ESCAPE study

Bone mineral density directly correlates with elevated serum leptin in haemodialysis patients

Maternal uniparental heterodisomy of chromosome 17 in a patient with nephropathic cystinosis

Measuring cervical length with ultrasound: evaluation of the procedures and duration of a learning method

Importance of vitamin D repletion in uraemia

Spi-1 PU.1 but not Fli-1 inhibits erythroid-specific alternative splicing of 4.1R pre-mRNA in murine erythroleukemia cells

Sevelamer hydrochloride with or without alphacalcidol or higher dialysate calcium vs calcium carbonate in dialysis patients: an open‐label, randomized study

Protein 4.1R expression in normal and dystrophic skeletal muscle

Percutaneous recanalization of occlusion of central and proximal veins in chronic hemodialysis: Technical Note

Magnesium Hydroxide as a Complementary Aluminium-free Phosphate Binder to Moderate Doses of Oral Calcium in Uraemic Patients on Chronic Haemodialysis: Lack of Deleterious Effect on Bone Mineralisation

Reactivation of Optic Nerve Head Astrocytes by TGF-β2 and H2O2 Is Accompanied by Increased Hsp32 and Hsp47 Expression

Comparison of intact, midregion, and carboxy terminal assays of parathyroid hormone for the diagnosis of bone disease in hemodialyzed patients

7-84 PTH or aluminum antagonism in the resistance of uremic bone to the remodeling effect of endogenous PTH? Author's reply

Prevention of osteitis fibrosa, aluminium bone disease and soft-tissue calcification in dialysis patients: a long-term comparison of moderate doses of oral calcium±Mg(OH)2 vs Al(OH)3±1α OH vitamin D3

Erosive osteoarthropathy associated with β2-microglobulin amyloidosis in a uraemic patient treated exclusively by long-term haemofiltration with biocompatible membranes

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