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Autosomal dominant Charcot-Marie-Tooth disease type 2B
Autosomal dominant Charcot-Marie-Tooth disease type 2C
Autosomal dominant Charcot-Marie-Tooth disease type 2D
Autosomal dominant Charcot-Marie-Tooth disease type 2E
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Autosomal dominant Charcot-Marie-Tooth disease type 2K
Autosomal dominant Charcot-Marie-Tooth disease type 2L
Autosomal dominant Charcot-Marie-Tooth disease type 2N
Autosomal dominant Charcot-Marie-Tooth disease type 2U

Translation of "charcot-marie-tooth disease type " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth type 4B2
SNOMEDCT-BE (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso / 715800000
SNOMEDCT-BE (disorder) / 715800000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2C
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maladie de Charcot-Marie-Tooth autosomique dominante type 2C
SNOMEDCT-BE (disorder) / 717010007
SNOMEDCT-BE (disorder) / 717010007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2L
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2L
SNOMEDCT-BE (disorder) / 719513008
SNOMEDCT-BE (disorder) / 719513008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2B
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2B
SNOMEDCT-BE (disorder) / 717008005
SNOMEDCT-BE (disorder) / 717008005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2K
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2K
SNOMEDCT-BE (disorder) / 719512003
SNOMEDCT-BE (disorder) / 719512003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2N
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2N
SNOMEDCT-BE (disorder) / 719515001
SNOMEDCT-BE (disorder) / 719515001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2D
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2D
SNOMEDCT-BE (disorder) / 717011006
SNOMEDCT-BE (disorder) / 717011006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2E
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2E
SNOMEDCT-BE (disorder) / 717012004
SNOMEDCT-BE (disorder) / 717012004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2U
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2U
SNOMEDCT-BE (disorder) / 765046002
SNOMEDCT-BE (disorder) / 765046002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Autosomal dominant Charcot-Marie-Tooth disease type 2I
https://browser.ihtsdotools.or (...) (...) [HTML]
maladie de Charcot-Marie-Tooth autosomique dominante type 2I
SNOMEDCT-BE (disorder) / 717013009
SNOMEDCT-BE (disorder) / 717013009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS
However, more than 50% of rare diseases only appear during adulthood, such as Huntington disease, Crohn's disease, Charcot-Marie-Tooth disease, amyotrophic lateral sclerosis, Kaposi's sarcoma, or thyroid cancer.
http://www.cihr-irsc.gc.ca/e/4 (...) (...) [HTML]
Toutefois, plus de 50 % des maladies rares ne surviennent qu'à l'âge adulte, comme la maladie de Huntington, la maladie de Crohn, la maladie de Charcot-Marie-Tooth, la sclérose latérale amyotrophique, la maladie de Kapos ou le cancer de la thyroïde.
http://www.cihr-irsc.gc.ca/e/4 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/f/4 (...) [HTML]
Linking faulty gene to MS Allison Kraus, a PhD student working with Dr. Marek Michalak, discovers that a misfiring gene called calnexin appears to contribute to multiple sclerosis and a related disorder called Charcot-Marie-Tooth disease.
http://www.cihr-irsc.gc.ca/e/3 (...) (...) [HTML]
Un gène défectueux en cause dans la SP Allison Kraus, étudiante au doctorat qui travaille au laboratoire du Dr Marek Michalak, découvre qu'un gène dysfonctionnel appelé calnexine semble contribuer à l'apparition de la sclérose en plaques et à un trouble connexe appelé maladie de Charcot-Marie-Tooth.
http://www.cihr-irsc.gc.ca/e/3 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/f/3 (...) [HTML]
have a particular form (called the " demyelinating form" ) of a condition called Charcot-Marie-Tooth syndrome
http://www.healthierchoices.ca (...) (...) [HTML]
la présence d'une forme particulière (appelée la forme démyélinisante) d'une affection appelée le syndrome de Charcot-Marie-Tooth.
http://www.healthierchoices.ca (...) (...) [HTML]
http://fr.healthierchoices.ca/ (...) [HTML]


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Date index:2022-08-14 -

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