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'common variable'-agammaglobulinemie
'common variable'-immunodeficiëntie
CVA-gamma
Hypogammaglobulinemie NNO

Vertaling van "common evaluation " (Nederlands → Frans) :

TERMINOLOGIE
agammaglobulinemie met immunoglobulinedragende B-lymfocyten | 'common variable'-agammaglobulinemie [CVA-gamma] | hypogammaglobulinemie NNO

Agammaglobulinémie:avec lymphocytes B porteurs d'immunoglobulines | commune variable | Hypogammaglobulinémie SAI


'common variable'-immunodeficiëntie met hoofdzakelijk afwijkingen van aantallen en functie van B-cellen

Déficit immunitaire commun variable avec anomalies prédominantes du nombre et de la fonction des lymphocytes B




'common variable'-immunodeficiëntie met hoofdzakelijk immunoregulatoire T-cel stoornissen

Déficit immunitaire commun variable avec anomalies prédominantes des lymphocytes T immunorégulateurs


'common variable'-immunodeficiëntie met autoantilichamen tegen B- of T-cellen

Déficit immunitaire commun variable avec autoanticorps anti-lymphocytes B ou T


overige gespecificeerde 'common variable'-immunodeficiënties

Autres déficits immunitaires communs variables
IN-CONTEXT TRANSLATIONS
- 2 e waarneming Definitief stoppen Niet van toepassing * Volgens de “National Cancer Institute of Canada Clinical Trial Group” (NCIC CTG) Common Toxicity Criteria (versie 1) van de “Common Terminology Criteria for Adverse Events” (CTCAE) van het “Cancer Therapy Evaluation Program, US National Cancer Institute, versie 3.0”.

- 2 e apparition Arrêter le traitement définitivement Sans objet * Conformément aux critères de toxicité du NCIC CTG (National Cancer Institute of Canada Clinical Trial Group) (version 1) ou aux critères du CTEP (Cancer Therapy Evaluation Program) pour les CTCAE (Common Terminology Criteria for Adverse Events) du programme d’évaluation des traitements anticancéreux de l’US National Cancer Institute (version 3.0).


The Clinical Trial Facilitation Group (CTFG) is a collaborative effort to facilitate and harmonise clinical trials in Europe. Within the CTFG agreements have been made for various competent authorities to voluntarily arrive at a common evaluation for applications for clinical trials whenever this involves multicentre trials with participating centres from different Member States.

The Clinical Trial Facilitation Group (CTFG) is a collaborative effort to facilitate and harmonise clinical trials in Europe. Within the CTFG agreements have been made for various competent authorities to voluntarily arrive at a common evaluation for applications for clinical trials whenever this involves multicentre trials with participating centres from different Member States.




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Date index: 2021-12-15
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