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Autres neuropathies héréditaires et idiopathiques
Déjerine-Sottas
Hypertrophique de l'enfant
Neuropathie héréditaire et idiopathique
Neuropathie héréditaire motrice et sensorielle
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie sensitive
Récessive
Syndrome de Nélaton
Syndrome de Roussy-Lévy

Translation of "neuropathie héréditaire sensitive " (French → English) :

TERMINOLOGY
see also In-Context Translations below
neuropathie héréditaire sensitive et autonomique
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique avec surdité et retard de développement
https://browser.ihtsdotools.or (...) (...) [HTML]
This syndrome has characteristics of sensory and autonomic axonal neuropathy, sensorineural hearing loss and persistent global developmental delay. It has been described in four individuals from a consanguineous Lebanese family. Onset occurred in inf
SNOMEDCT-BE (disorder) / 717826009
SNOMEDCT-BE (disorder) / 717826009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1B
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Neuropathie héréditaire et idiopathique
https://icd.who.int/browse10/2 (...) (...) [HTML]
Hereditary and idiopathic neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60
WORLD HEALTH ORGANIZATION ICD-10: G60
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy
https://icd.who.int/browse10/2 (...) (...) [HTML]
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Neuropathie héréditaire motrice et sensorielle
https://icd.who.int/browse10/2 (...) (...) [HTML]
Hereditary motor and sensory neuropathy
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Autres neuropathies héréditaires et idiopathiques
https://icd.who.int/browse10/2 (...) (...) [HTML]
Other hereditary and idiopathic neuropathies
WORLD HEALTH ORGANIZATION ICD-10: G60.8
WORLD HEALTH ORGANIZATION ICD-10: G60.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton
https://icd.who.int/browse10/2 (...) (...) [HTML]
Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited
WORLD HEALTH ORGANIZATION ICD-10: G60.8
WORLD HEALTH ORGANIZATION ICD-10: G60.8
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
neuropathie sensitive
https://browser.ihtsdotools.or (...) (...) [HTML]
Sensory neuropathy
SNOMEDCT-BE (disorder) / 95662005
SNOMEDCT-BE (disorder) / 95662005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS
Ces nouvelles connaissances sont issues d'une étude subventionnée par les IRSC et intitulée « Le transporteur axonal des vésicules synaptiques K1F1A mute en neuropathie sensitive et autonomique héréditaire de type 2 », publiée dans la revue American Journal of Human Genetics .
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
The findings were reported in a study entitled " The axonal transporter of synaptic vesicles KIF1A is mutated in hereditary sensory and autonomic neuropathy type 2" . The study was published in the American Journal of Human Genetics and was supported by a grant from CIHR.
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/e/4 (...) [HTML]


Others have searched : autres neuropathies héréditaires et idiopathiques    déjerine-sottas    neuropathie héréditaire et idiopathique    neuropathie héréditaire motrice et sensorielle    syndrome de nélaton    syndrome de roussy-lévy    hypertrophique de l'enfant    neuropathie héréditaire sensitive et autonomique    neuropathie sensitive    récessive    neuropathie héréditaire sensitive    


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neuropathie héréditaire sensitive

Date index:2021-02-11 -

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