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Enzym
Enzym voor stamcelwinning uit vetweefsel
Giststof
Humane alfa-1-proteinase inhibitor

Vertaling van "enzym inhibitor " (Nederlands → Frans) :

TERMINOLOGIE
blootstelling aan remmingsmiddel angiotensine-omzettend enzym

exposition à un agent inhibiteur de l'enzyme de conversion de l'angiotensine


enzym voor stamcelwinning uit vetweefsel

enzyme de récupération de cellules souches du tissu adipeux






acute myeloïde leukemie en myelodysplastische syndromen gerelateerd aan topo-isomerase type 2-inhibitor

leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux inhibiteurs de la topoisomérase II
IN-CONTEXT TRANSLATIONS
Tabel 9. Hoeveelheid antibioticumgebruik van de 30 meest voorgeschreven molecules. Molecule ATC a DDD b % Amoxicilline + enzym inhibitor J01CR02 680 278 25,96 Nifurtoinol J01XE02 194 335 7,42 Ciprofloxacine J01MA02 177 904 6,79 Cefuroxime J01DC02 172 838 6,60 Amoxicilline J01CA04 168 054 6,41 Nitrofurantoin J01XE01 102 860 3,92 Levofloxacine J01MA12 89 393 3,41 Fluconazole J02AC01 87 007 3,32 Sulfamethoxazole + trimethoprim J01EE01 75 514 2,88 Flucloxacilline J01CF05 65 352 2,49 Terbinafine D01BA02 61 782 2,36 Clarithromycine J01FA09 61 123 2,33 Moxifloxacine J01MA14 58 519 2,23 Ofloxacine J01MA01 55 923 2,13 Itraconazole J02AC02 50 684 ...[+++]

Molécule ATC a DDD b % Amoxicilline + inhibiteur d’enzymes J01CR02 680.278 25,96 Nifurtoïnol J01XE02 194.335 7,42 Ciprofloxacine J01MA02 177.904 6,79 Céfuroxime J01DC02 172.838 6,60 Amoxicilline J01CA04 168.054 6,41 Nitrofurantoïne J01XE01 102.860 3,92 Levofloxacine J01MA12 89.393 3,41 Fluconazole J02AC01 87.007 3,32 Sulfaméthoxazole + triméthoprime J01EE01 75.514 2,88 Flucloxacilline J01CF05 65.352 2,49 Terbinafine D01BA02 61.782 2,36 Clarithromycine J01FA09 61.123 2,33 Moxifloxacine J01MA14 58.519 2,23 Ofloxacine J01MA01 55.923 2,13 Itraconazole J02AC02 50.684 1,93 Doxycycline J01AA02 45.333 1,73 Norfloxacine J01MA06 38.232 1,46 Clinda ...[+++]


Amoxicilline + enzyme inhibitor Amoxicilline + clavulaanzuur 1.000 mg

Amoxicilline + acide clavulanique Amoxicilline + acide clavulanique 1.000 mg




hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic.

26Octobre1999 ( [http ...]


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Lancet 362, 782-788 (2003) H.D. White: Should all patients with coronary disease receive angiotensin-converting-enzyme inhibitors?

Lancet 362, 782-788 (2003) H.D. White: Should all patients with coronary disease receive angiotensin-convertingenzyme inhibitors?


L.M.H.Wing et al.: A comparison of outcomes with angiotensin-converting-enzyme inhibitors and diuretics for hypertension in the elderly.

D’après The ALLHAT Officers and Coordinators for the ALLAHT Collaborative Research Group. Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic.


Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs diuretic.

Major outcomes in high-risk hypertensive patients randomized to angiotensin converting enzyme inhibitor or calcium channel blocker vs diuretic.


2 Effectiveness of spironolactone added to an angiotensin - converting enzyme inhibitor and a loop diuretic for severe chronic congestive heart failure, Am. J. Cardiol. 1996 oct 15; 78 (8 ):902-7

2 Effectiveness of spironolactone added to an angiotensin - converting enzyme inhibitor and a loop diuretic for


R.W. Schrier en R.O. Estacio: The effect of angiotensin-converting enzyme inhibitors on the progression of nondiabetic renal disease: a pooled analysis of individual-patient data from 11 randomized, controlled trials (Editoriaal) Ann Intern Med 135 : 138-139(2001)

R.W. Schrier en R.O. Estacio: The effect of angiotensin-converting enzyme inhibitors on the progression of nondiabetic renal disease: a pooled analysis of individual-patient data from 11 randomized, controlled trials (Editorial) Ann Intern Med 135 : 138-139(2001)


Het voorbeeld van het azoolderivaat fluconazol is slecht gekozen: fluconazol is een potente inhibitor van het CYP2C9 iso-enzym, een enzym dat tussenkomt in de afbraak van b.v. warfarine en fenytoïne, maar slechts een zwakke inhibitor van het CYP3A4 iso-enzym.

L’exemple du dérivé azolique fluconazole a été mal choisi: le fluconazole est un inhibiteur puissant de l’isoenzyme CYP2C9, une enzyme qui intervient dans le métabolisme de la warfarine ou de la phénytoïne par exemple, mais n’est qu’un inhibiteur faible de l’isoenzyme CYP3A4.




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Date index: 2025-06-18
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