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305).
the
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
c.305 c>g
c.307 g>c
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
Waarschuwing: Bevat onzichtbare HTML-opmaak
305 (80,5)a
305 (80.5)a
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
305 74770 opava-komarov tékkland
305 74770 opava-komarov czech republic
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
305, 74770 opava-komarov tékkland
305, 74770 opava-komarov czech republic
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
305, 74770 opava-komarov, tékkland
305, 74770 opava-komarov, czech republic
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
rannsókn 301 (n=305; n=256)
study 301 (n=305; n=256)
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
eftir markaðssetningu var greint frá 305 tilvikum sundls.
in post-marketing data, 305 cases of dizziness were reported.
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
grein 305 grein 306 grein 307 grein 308 grein 309 alls
grand total
Laatste Update: 2014-02-06
Gebruiksfrequentie: 1
Kwaliteit:
eftir skráningu 305 sjúklinga í rannsóknir 4 og 5 var sjálfstæð afturvirk endurskoðun gerð á upplýsingum frá geislagreiningu.
upon enrolment of 305 patients in studies 4 and 5 a retrospective independent review of radiographic imaging data was performed.
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
athugið: samhliða and-her2 meðferð var ekki tekin með í rannsókn 305 og rannsókn 301.
note: concomitant anti-her2 therapy was not included in study 305 and study 301.
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit:
af öllum sjúklingunum var ekki hægt að meta hvort um mmr var að ræða eftir 48 mánuði hjá alls 305 (36,1%) (98 í hópnum sem fékk nilotinib 300 mg tvisvar á sólarhring, 88 í hópnum sem fékk nilotinib 400 mg tvisvar á sólarhring og 119 í hópnum sem fékk imatinib) vegna vöntunar/ómetanlegra pcr mælinga (n=18), ódæmigerðrar umritunar við grunnlínu (n=8), eða vegna þess að þeir höfðu hætt áður en komið var að 48-mánaða tímapunktinum (n=279).
a total of 305 (36.1%) of all patients were not evaluable for mmr at 48 months (98 in the nilotinib 300 mg bid group, 88 in the nilotinib 400 mg bid group and 119 in the imatinib group) due to missing/unevaluable pcr assessments (n=18), atypical transcripts at baseline (n=8), or discontinuation prior to the 48-month time point (n=279).
Laatste Update: 2017-04-26
Gebruiksfrequentie: 1
Kwaliteit: