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Gamma globulin
Gamma-E globulin
High-affinity immunoglobulin E receptor
Humanized anti-IgE therapy
Humanized anti-immunoglobulin E therapy
IgE
IgG
Immunoglobulin E
Immunoglobulin G
Immunoglobulin IgE
Immunoglobulin gamma
Serum IgE
Serum immunoglobulin E

Translation of "Serum immunoglobulin E " (English → French) :

TERMINOLOGY
see also In-Context Translations below
serum IgE | serum immunoglobulin E

IgE sérique | immunoglobuline E sérique
IATE - Health
IATE - Health


immunoglobulin E | IgE | gamma-E globulin

immunoglobulines E | IgE | IgND
biologie
biologie


immunoglobulin E

immunoglobuline E
Immunology
Immunologie


high-affinity immunoglobulin E receptor

récepteur de haute affinité pour l'immunoglobuline E
Immunology
Immunologie


humanized anti-IgE therapy [ humanized anti-immunoglobulin E therapy ]

thérapie à base d'anticorps anti-IgE humanisés [ thérapie à base d'anticorps anti-immunoglobuline E ]
Immunology | Non-Surgical Treatment
Immunologie | Traitements non chirurgicaux


gamma globulin | immunoglobulin G | immunoglobulin gamma | IgG [Abbr.]

gamma globuline | gammaglobuline | immunoglobuline G | IgG [Abbr.]
IATE - Health
IATE - Health


immunoglobulin E | immunoglobulin IgE | IgE [Abbr.]

immunoglobuline E | IgE [Abbr.]
IATE - Health
IATE - Health


A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL

myopathie métabolique par défaut de transport du lactate
SNOMEDCT-BE (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL / 766715000
SNOMEDCT-BE (disorder) / 766715000


This syndrome is characterized by psychomotor delay and severe myopathy (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr

retard psychomoteur par déficit en S-adénosylhomocystéine hydrolase
SNOMEDCT-BE (hypotonia, absent tendon reflexes and delayed myelination) from birth, associated with hypermethioninemia and elevated serum creatine kinase levels. It has been described in thr / 724039002
SNOMEDCT-BE (disorder) / 724039002


A rare genetic epidermal disorder with characteristics of congenital erythroderma with severe psoriasiform dermatitis, ichthyosis, severe palmoplantar keratoderma, yellow keratosis on the hands and feet, elevated immunoglobulin E, multiple food aller

syndrome de dermatite sévère-allergies multiples-cachexie métabolique
SNOMEDCT-BE (disorder) / 774211005
SNOMEDCT-BE (disorder) / 774211005
IN-CONTEXT TRANSLATIONS
Rabbit anti-guinea-pig immunoglobulin conjugated to horseradish peroxidase is used at a predetermined optimum concentration in PBST containing 10 % normal bovine serum and 5 % normal rabbit serum.

Utiliser de l'immunoglobuline de lapin anticobaye conjuguée à de la peroxydase de raifort à une concentration optimale prédéterminée dans le PBST contenant 10 % de sérum de bovin normal et 5 % de sérum de lapin normal.




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'Serum immunoglobulin E'

Date index:2024-04-22 -

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