What is the translation of " IS PRESENTED IN TABLE " in Croatian?

[iz pri'zentid in 'teibl]
[iz pri'zentid in 'teibl]

Examples of using Is presented in table in English and their translations into Croatian

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The dosing schedule is presented in Table 1.
Raspored doziranja prikazan je u Tablici 1.
The distribution of patients by age and minimum, median andmaximum dose received during the OL LI phase is presented in Table 4.
Raspored bolesnika prema dobi te minimalnoj imaksimalnoj dozi i medijanu doze tijekom ove faze prikazan je u Tablici 4.
A summary of results is presented in Table 3.
Sažetak rezultata prikazan je u Tablici 3.
A cohort of 763 patients within Studies I and II met this criterion;the primary efficacy outcome is presented in Table 3.
Ovaj je kriterij zadovoljila kohorta od 763 bolesnika u Ispitivanjima I i II, aprimarni ishod djelotvornosti prikazan je u tablici 3.
The recommended dosing regimen is presented in Tables 2 and 3.
Preporučeni režim doziranja nalazi se u tablicama 2 i 3.
The incidence of both ACUITY-scale and TIMI-scale bleeding events up to day 30 for the intent-to- treat population is presented in Table 6.
Incidencija krvarenja, prema ljestvicama ACTUITY i TIMI, do 30 dana u populaciji s namjerom liječenja(ITT) prikazana je u tablici 6.
A summary of pharmacokinetic data is presented in Table 1.
Sažetak farmakokinetičkih podataka nalazi se u Tablici 1.
Vaccine efficacy against high grade cervical lesions associated with HPV-16/18 observed in TVC at end of study is presented in Table 3.
Djelotvornost cjepiva protiv cervikalnih lezija visokog stupnja, povezanih sa HPV-16/18, a koje su uočene u TVC na kraju ispitivanja, prikazana je u Tablici 3.
A tabular summary of the secondary efficacy results is presented in Table 3.
Sažetak sekundarnih rezultata djelotvornosti prikazan je u tablici 3.
Vaccine efficacy against virological endpoints(6-month and 12-month persistent infection)associated with HPV-16/18 observed in TVC at end of study is presented in Table 4.
Djelotvornost cjepiva na virološke ishode(6-mjesečne i 12-mjesečne perzistentne infekcije)povezane sa HPV-16/18 uočene u TVC na kraju ispitivanja prikazana je u Tablici 4.
Vaccine efficacy against the primary endpoint CIN2+ is presented in Table 1.
Djelotvornost cjepiva prema primarnom ishodu CIN 2+ prikazana je u Tablici 1.
Vaccine efficacy against virological endpoints(6-month and 12-month persistent infection)associated with HPV-16/18 observed in the ATP cohort at the end of study is presented in Table 2.
Djelotvornost cjepiva protiv viroloških ishoda(6-mjesečna i 12-mjesečna perzistentna infekcija)povezana sa HPV-16/18, uočena u ATP kohorti na kraju ispitivanja, prikazana je u Tablici 2.
The response to treatment in both of these trials is presented in Table 13.
Terapijski odgovor u oba ispitivanja prikazan je u Tablici 13.
Short term monotherapy data of simeprevir from studies C201(genotype 1) and C202(genotype 2, 3, 4, 5 and 6)in patients receiving 200 mg once daily simeprevir for 7 days is presented in table 9.
Podaci iz kratkotrajnog liječenja simeprevirom u monoterapiji iz ispitivanja C201(genotip 1) iC202(genotip 2, 3, 4, 5 i 6) u bolesnika koji uzimaju 200 mg simeprevira jedanput na dan tijekom 7 dana prikazani su u tablici 9.
The response to treatment in both of these trials is presented in Table 11.
Odgovor na liječenje u oba ispitivanja prikazan je u tablici Tablica 11.
A subgroup analysis of the virologic response(defined as a viral load< 50 HIV-1 RNA copies/ml) at week 48 by baseline viral load andbaseline CD4 count(pooled DUET data) is presented in table 4.
Analiza virološkog odgovora podskupina(definiranog kao virusno opterećenje< 50 HIV-1 RNK kopija/ml) u 48. tjednu na temelju početnog virusnog opterećenja ipočetnog broja CD4 stanica(udruženi podaci ispitivanja DUET) prikazani su u tablici 4.
The detailed spending of the financial allocation for 2006-2014 is presented in Table 1 in Annex.
Detaljan prikaz potrošnje financijskih sredstava u razdoblju od 2006. do 2014. nalazi se u tablici 1. u Prilogu.
Investigator analysis on data at the end of enrolment is presented in Table 1.
Ispitivačeva analiza podataka nakon završetka uključivanja prikazana je u tablici 1.
Vaccine efficacy against the primary endpoint CIN2+ at the end of study is presented in Table 1.
Djelotvornost cjepiva prema primarnom ishodu CIN 2+ prikazana je u Tablici 1.
The share of energy from renewable sources in heating and cooling is presented in Table 4.
Udio energije iz obnovljivih izvora u grijanju i hlađenju naveden je u tablici 4.
A summary of action as a function of the test results during treatment with Zinbryta is presented in table 1 below.
Sažetak potrebnih mjera prema rezultatima testova tijekom liječenja Zinbrytom prikazan je u tablici 1 u nastavku.
The investigator radiographic review of rPFS performed as a follow up sensitivity analysis is presented in Table 3 and Figure 2.
Radiografski pregled ispitivača rPFS proveden kao nastavna analiza osjetljivosti, prikazan je u Tablici 3 i na Slici 2.
The immune responses elicited by IXIARO are presented in Table 10.
Imunološki odgovori na IXIARO prikazani su u tablici 10.
Treatment outcomes of study GS-US-311-1089 through 48 weeks are presented in Table 6.
Ishodi liječenja u ispitivanju GS-US-311-1089 do kraja 48. tjedna prikazani su u Tablici 6.
The efficacy results of the study are presented in Table 14.
Rezultati djelotvornosti za ovo ispitivanje prikazani su u Tablici 14.
The result with respect to the primary endpoint study are presented in Table 5.
Rezultati u pogledu primarnog ishoda ispitivanja prikazani su u tablici 5.
The results of AI455-099 and AI455-096 are presented in Table 1.
Rezultati AI455-099 i AI455-096 ispitivanja prikazani su u Tablici 1.
The key results from the study are presented in tables 4.
Ključni rezultati ispitivanja prikazani su u tablici 4.
The results are presented in Table 2.
Rezultati su prikazani u Tablici 2.
The study design andpatient demographics are presented in Table 2.
Dizajn studije idemografija bolesnika su prikazani u tablici 2.
Results: 30, Time: 0.0503

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