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Céphalée trigémino-autonomique
Dénervation sensitive
Fonction sensitive
Insuffisance autonomique primaire
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie sensitive

Translation of "sensitive et autonomique " (French → English) :

TERMINOLOGY
see also In-Context Translations below
neuropathie héréditaire sensitive et autonomique

Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005


neuropathie héréditaire sensitive et autonomique avec surdité et retard de développement

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


neuropathie héréditaire sensitive et autonomique type 1B

Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008


neuropathie héréditaire sensitive et autonomique type 1

Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008


céphalée trigémino-autonomique

Trigeminal autonomic cephalgia
SNOMEDCT-BE (disorder) / 449814007
SNOMEDCT-BE (disorder) / 449814007


insuffisance autonomique primaire

Autonomic failure
SNOMEDCT-CA (trouble) / 84438001
SNOMEDCT-CA (trouble) / 84438001


neuropathie sensitive

Sensory neuropathy
SNOMEDCT-BE (disorder) / 95662005
SNOMEDCT-BE (disorder) / 95662005


fonction sensitive

Sensory function
SNOMEDCT-CA (entité observable) / 106148006
SNOMEDCT-CA (entité observable) / 106148006


dénervation sensitive

Deafferentation
SNOMEDCT-CA (constatation) / 28502008
SNOMEDCT-CA (constatation) / 28502008


neuropathie sensitive congénitale avec perte sélective des petites fibres myélinisées

Hereditary sensory and autonomic neuropathy type V
SNOMEDCT-CA (trouble) / 128206006
SNOMEDCT-CA (trouble) / 128206006
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 .

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.




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sensitive et autonomique

Date index:2021-06-27 -

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