D. Simon

发表

Human Hypertension Caused by Mutations in WNK Kinases

Robert J. Unwin, Murat Gunel, Kazuhiko Ishikawa, 2001, Science.

Symptomatic osseous sarcoidosis with findings on bone scan.

D. Simon, A. Shirkhoda, H. M. Silver, 1978, Chest.

Heterochromia pardus: implications of the spotted pale iris

D. Simon, L. Forstot, J. Austin, 1982 .

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

R. Lifton, D. Simon, D. Cruz, 2001, Kidney international.

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

A. Kliger, N. Levin, F. Gotch, 2004, Blood Purification.

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

R. Lifton, H. Trachtman, D. Simon, 2000, Pediatric Nephrology.

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

R. Lifton, D. Simon, 1998, Current opinion in cell biology.

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

R. Lifton, D. Simon, 1998, Clinical and Experimental Nephrology.

Ion transporter mutations in Gitelman's and Bartter's syndromes

R. Lifton, D. Simon, 1998, Current opinion in nephrology and hypertension.

Calcimimetics for the Treatment of Secondary Hyperparathyroidism in Peritoneal Dialysis Patients

D. Simon, F. Finkelstein, J. Francis, 2008 .

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

Hongyu Zhao, Daniel Levy, Weizhen Ji, 2008, Nature Genetics.

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

R. Lifton, C. Nelson-Williams, D. Ellison, 1996, Nature Genetics.

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

D. Simon, J. Francis, F. Finkelstein, 2007, Advances in peritoneal dialysis. Conference on Peritoneal Dialysis.

Strontium-87m lung scans in pulmonary aspergillosis.

R. Reba, D. Simon, R. Goldstein, 1977, AJR. American journal of roentgenology.

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

R. Lifton, K. Finberg, C. Nelson-Williams, 2001, Hypertension.

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

T. Mansfield, R. Lifton, A. Nayır, 1997, Nature Genetics.

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

R. Lifton, S. Sanjad, H. Trachtman, 1996, Nature Genetics.

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

R. Lifton, S. Sanjad, D. Simon, 1996, Nature genetics.

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

R. Lifton, S. Sanjad, D. Milford, 1999, Science.

Neuropsychological findings in myotonic dystrophy.

R. Heaton, D. Simon, S. Ringel, 1982, Journal of clinical neuropsychology.

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

R. Lifton, S. Sanjad, A. Pietro, 1996, Nature Genetics.

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

R. Lifton, D. Simon, 1996, The American journal of physiology.

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

N. Risch, T. Mansfield, R. Lifton, 1997, Nature Genetics.

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

D. Simon, F. Finkelstein, Jaya Gobin, 2012 .

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

D. Simon, F. Finkelstein, Jaya Gobin, 2012, Clinical drug investigation.

Luetic meningitis with gumma

D. Simon, 1982, Neurology.