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Tolvaptan in Patients with Autosomal Dominant Polycystic Kidney Disease

Author
TORRES, Vicente E1 ; CHAPMAN, Arlene B2 ; DEVUYST, Olivier3 4 ; GANSEVOORT, Ron T5 ; GRANTHAM, Jaredj6 ; HIGASHIHARA, Eiji7 ; PERRONE, Ronald D8 ; KRASA, Holly B9 ; OUYANG, John9 ; CZERWIEC, Frank S9
[1] Division of Nephrology and Hypertension, Department of Internal Medicine, Mayo Clinic, Rochester, MN, United States
[2] Division of Nephrology, Emory University School of Medicine, Atlanta, United States
[3] Division of Nephrology, Cliniques Universitaires St. Luc, Université Catholique de Louvain Medical School, Brussels, Belgium
[4] Institute of Physiology, Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland
[5] Division of Nephrology, Department of Internal Medicine, University Medical Center Groningen, University of Groningen, Groningen, Netherlands
[6] Kidney Institute and the Department of Internal Medicine, Kansas University Medical Center, Kansas City, United States
[7] Department of Urology, Kyorin University School of Medicine, Mitaka, Japan
[8] Department of Medicine, Division of Nephrology, Tufts Medical Center, Tufts University School of Medicine, Boston, United States
[9] Otsuka Pharmaceutical Development and Commercialization, Rockville, MD, United States
TEMPO 3:4 Trial Investigators
Source

The New England journal of medicine. 2012, Vol 367, Num 25, pp 2407-2418, 12 p ; ref : 36 ref

CODEN
NEJMAG
ISSN
0028-4793
Scientific domain
General medicine general surgery
Publisher
Massachusetts Medical Society, Waltham, MA
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Autosome Homme Hérédité Malade Maladie héréditaire Médecine Néphropathie Pathologie du rein Rein polykystique Tolvaptan Antagoniste Hormone neurohypophysaire Kyste Neuropeptide Pathologie de l'appareil urinaire Récepteur peptidergique Récepteur vasopressine V2 Tumeur bénigne Vasopressine
Keyword (en)
Autosome Human Inheritance(genetics) Patient Genetic disease Medicine Nephropathy Kidney disease Polycystic kidney Tolvaptan Antagonist Neurohypophyseal hormone Cyst Neuropeptide Urinary system disease Peptidergic receptor V2 vasopressin receptor Benign neoplasm Vasopressin
Keyword (es)
Autosoma Hombre Herencia(genética) Enfermo Enfermedad hereditaria Medicina Nefropatía Riñón patología Riñón poliquístico Tolvaptán Antagonista Hormona neurohipofisaria Quiste Neuropéptido Aparato urinario patología Receptor peptidérgico Receptor vasopresina V2 Tumor benigno Vasopresina
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B01 General aspects

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B14 Nephrology. Urinary tract diseases / 002B14C Malformations of the urinary system / 002B14C01 Kidneys

Discipline
Generalities in medical sciences Nephrology. Urinary tract diseases
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
26727157

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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