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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Nature genetics, 2008-05, Vol.40 (5), p.592-599

2008

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Mutations in the Na-Cl Cotransporter Reduce Blood Pressure in Humans

Hypertension (Dallas, Tex. 1979), 2001-06, Vol.37 (6), p.1458-1464

2001

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Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21

Nature genetics, 1997-06, Vol.16 (2), p.202-205

1997

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Human Hypertension Caused by Mutations in WNK Kinases

Science (American Association for the Advancement of Science), 2001-08, Vol.293 (5532), p.1107-1112

2001

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Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

Science (American Association for the Advancement of Science), 1999-07, Vol.285 (5424), p.103-106

1999

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Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life

Kidney international, 2001-02, Vol.59 (2), p.710-717

2001

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Mutations in the chloride channel gene, CLCNKB , cause Bartter's syndrome type III

Nature genetics, 1997-10, Vol.17 (2), p.171-178

1997

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Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2CI cotransporter NKCC2

Nature genetics, 1996-06, Vol.13 (2), p.183-188

1996

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Bartter syndrome and focal segmental glomerulosclerosis : a possible link between two diseases

Pediatric nephrology (Berlin, West), 2000-09, Vol.14 (10-11), p.970-972

2000

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Conversion from Epoetin Alfa to Darbepoetin Alfa for Management of Anaemia in a Community Chronic Kidney Disease Centre: A Retrospective Cohort Study

Clinical drug investigation, 2011-02, Vol.31 (2), p.113-120

2011

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Conversion from Epoetin Alfa to Darbepoetin Alfa for Management of Anaemia in a Community Chronic Kidney Disease Centre: A Retrospective Cohort Study

Clinical drug investigation, 2011, p.1

2011

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Calcimimetics for the Treatment of Secondary Hyperparathyroidism in Peritoneal Dialysis Patients

Peritoneal dialysis international, 2008-03, Vol.28 (2_suppl), p.42-46

2008

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A One-Year Trial of In-Center Daily Hemodialysis with an Emphasis on Quality of Life

Blood purification, 2004-01, Vol.22 (3), p.320-328

2004

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Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes

Current opinion in cell biology, 1998-08, Vol.10 (4), p.450-454

1998

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Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg$^{2+}$ Resorption

Science (American Association for the Advancement of Science), 1999-07, Vol.285 (5424), p.103-106

1999

Volltextzugriff (PDF)

Genetic heterogeneity of Barter's syndrome revealed by mutations in the K + channel, ROMK

Nature genetics, 1996-10, Vol.14 (2), p.152-156

1996

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Ion transporter mutations in Gitelmanʼs and Bartterʼs syndromes

Current opinion in nephrology and hypertension, 1998-01, Vol.7 (1), p.43-48

1998

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Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

Nature genetics, 1996-10, Vol.14 (2), p.152-156

1996

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Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Nature genetics, 1996-01, Vol.12 (1), p.24-30

1996

Volltextzugriff (PDF)

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Nature genetics, 1996, Vol.12 (1), p.24-30

1996

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Ion transporter and channel mutations in Bartter's and Gitelman's syndromes of inherited hypokalemic alkalosis

Clinical and experimental nephrology, 1998-09, Vol.2 (3), p.199-203

1998

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Conversion from Epoetin Alfa to Darbepoetin Alfa for Management of Anaemia in a Community Chronic Kidney Disease Centre

Clinical drug investigation, 2011-02, Vol.31 (2), p.113

2011

Volltextzugriff (PDF)

CALCIMIMETICS FOR THE TREATMENT OF SECONDARY HYPERPARATHYROIDISM IN PERITONEAL DIALYSIS PATIENTS: Chronic Kidney Disease

Peritoneal dialysis international, 2008, Vol.28

2008

Volltextzugriff (PDF)

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes

American journal of physiology. Renal physiology, 1996-11, Vol.271 (5), p.961-F966

1996

Volltextzugriff (PDF)

Metabolic lung disease: diffuse metastatic pulmonary calcifications with progression to calciphylaxis in end-stage renal disease

Advances in peritoneal dialysis, 2007, Vol.23, p.112

2007

Volltextzugriff (PDF)

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Rare independent mutations in renal salt handling genes contribute to blood pressure variation

Mutations in the Na-Cl Cotransporter Reduce Blood Pressure in Humans

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21

Human Hypertension Caused by Mutations in WNK Kinases

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

Gitelman's syndrome revisited: An evaluation of symptoms and health-related quality of life

Mutations in the chloride channel gene, CLCNKB , cause Bartter's syndrome type III

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2CI cotransporter NKCC2

Bartter syndrome and focal segmental glomerulosclerosis : a possible link between two diseases

Conversion from Epoetin Alfa to Darbepoetin Alfa for Management of Anaemia in a Community Chronic Kidney Disease Centre: A Retrospective Cohort Study

Conversion from Epoetin Alfa to Darbepoetin Alfa for Management of Anaemia in a Community Chronic Kidney Disease Centre: A Retrospective Cohort Study

Calcimimetics for the Treatment of Secondary Hyperparathyroidism in Peritoneal Dialysis Patients

A One-Year Trial of In-Center Daily Hemodialysis with an Emphasis on Quality of Life

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes

Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg$^{2+}$ Resorption

Genetic heterogeneity of Barter's syndrome revealed by mutations in the K + channel, ROMK

Ion transporter mutations in Gitelmanʼs and Bartterʼs syndromes

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Ion transporter and channel mutations in Bartter's and Gitelman's syndromes of inherited hypokalemic alkalosis

Conversion from Epoetin Alfa to Darbepoetin Alfa for Management of Anaemia in a Community Chronic Kidney Disease Centre

CALCIMIMETICS FOR THE TREATMENT OF SECONDARY HYPERPARATHYROIDISM IN PERITONEAL DIALYSIS PATIENTS: Chronic Kidney Disease

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes

Metabolic lung disease: diffuse metastatic pulmonary calcifications with progression to calciphylaxis in end-stage renal disease

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