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- Q65470581 description "clinical trial" @default.
- Q65470581 description "ensayu clínicu" @default.
- Q65470581 description "klinisch onderzoek" @default.
- Q65470581 description "клінічне випробування" @default.
- Q65470581 name "Long-term Efficacy, Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome (RLS)" @default.
- Q65470581 name "Long-term Efficacy, Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome (RLS)" @default.
- Q65470581 type Item @default.
- Q65470581 label "Long-term Efficacy, Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome (RLS)" @default.
- Q65470581 label "Long-term Efficacy, Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome (RLS)" @default.
- Q65470581 prefLabel "Long-term Efficacy, Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome (RLS)" @default.
- Q65470581 prefLabel "Long-term Efficacy, Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome (RLS)" @default.
- Q65470581 P1050 Q65470581-07A6EAE1-5457-43E2-A913-0979C574000F @default.
- Q65470581 P1050 Q65470581-67DE00C8-EC09-4E10-A609-3BE0470A31F0 @default.
- Q65470581 P1050 Q65470581-E683310E-1059-4F8E-99C2-F1C221EA25C0 @default.
- Q65470581 P1132 Q65470581-8079BD05-9DD0-49D7-BA46-1F69299FC576 @default.
- Q65470581 P1476 Q65470581-E835C188-E39C-4AE9-8563-F738587AA638 @default.
- Q65470581 P17 Q65470581-02D0DE83-976F-456B-BBB0-6D615F70CF26 @default.
- Q65470581 P17 Q65470581-1AD7EE24-AF19-49C9-A7FF-106F1F24EA78 @default.
- Q65470581 P17 Q65470581-383E9A3F-9BD7-44BC-A999-17E45BE21092 @default.
- Q65470581 P17 Q65470581-567FA962-23C3-482A-B448-43174B458A00 @default.
- Q65470581 P17 Q65470581-69AC8E2D-05F2-48CE-A38C-7014D94F9622 @default.
- Q65470581 P17 Q65470581-76428B3C-7C80-4F87-A007-B25A10E77237 @default.
- Q65470581 P17 Q65470581-926522F8-A3A1-406F-9738-99C7F535923B @default.
- Q65470581 P17 Q65470581-BA41F43B-B01D-4D68-BC8F-1C9A0D4E085D @default.
- Q65470581 P17 Q65470581-F6F79B8E-D419-429F-A088-3188EAEA6817 @default.
- Q65470581 P2899 Q65470581-8F017DEC-EE3B-4E0E-BFA5-333F8F83CBC3 @default.
- Q65470581 P3098 Q65470581-5FA5CE43-9786-4F70-AD12-6F20BF0686BA @default.
- Q65470581 P31 Q65470581-12D3D0A0-1E39-4EBE-A530-DA2B463DA6CC @default.
- Q65470581 P4135 Q65470581-45D98C56-062B-4BC6-AD61-632937F762E2 @default.
- Q65470581 P4844 Q65470581-8177D99B-4F4E-4E33-B90D-0466864F003D @default.
- Q65470581 P580 Q65470581-12160B1F-F6A9-4283-93F2-FA99DEC72B34 @default.
- Q65470581 P582 Q65470581-6DA2BB93-3F37-4F3F-982C-872FF205CBB2 @default.
- Q65470581 P6099 Q65470581-0E8DBAFA-8DBC-4429-B710-113859B3A84C @default.
- Q65470581 P8363 Q65470581-359F1AAB-612F-40A9-9B03-78B594AB8DBE @default.
- Q65470581 P1050 Q179630 @default.
- Q65470581 P1050 Q394129 @default.
- Q65470581 P1050 Q916280 @default.
- Q65470581 P1132 "+331" @default.
- Q65470581 P1476 "A Phase IV Randomised, Double-blind, Placebo-controlled, Dose Titration Trial With Pramipexole (Sifrol, Mirapexin) 0.125-0.75 mg/Day Per os to Investigate the Long-term Efficacy, Safety and Tolerability in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome for 26 Weeks Followed by a 26 Week Open-label Extension Treatment Period" @default.
- Q65470581 P17 Q145 @default.
- Q65470581 P17 Q183 @default.
- Q65470581 P17 Q214 @default.
- Q65470581 P17 Q27 @default.
- Q65470581 P17 Q29 @default.
- Q65470581 P17 Q31 @default.
- Q65470581 P17 Q33 @default.
- Q65470581 P17 Q40 @default.
- Q65470581 P17 Q55 @default.
- Q65470581 P2899 "+18" @default.
- Q65470581 P3098 "NCT00472199" @default.
- Q65470581 P31 Q30612 @default.
- Q65470581 P4135 "+85" @default.
- Q65470581 P4844 Q421304 @default.
- Q65470581 P580 "2007-05-01T00:00:00Z" @default.
- Q65470581 P582 "2008-07-01T00:00:00Z" @default.
- Q65470581 P6099 Q42825046 @default.
- Q65470581 P8363 Q78089383 @default.