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Déjerine-Sottas
Hypertrophique de l'enfant
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type 7
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivo-motrice héréditaire type 5
Neuropathie sensitivo-motrice héréditaire type Okinawa
Neuropathie sensitivomotrice héréditaire de type I
Neuropathie sensitivomotrice héréditaire type 4
Syndrome de Roussy-Lévy

Translation of "neuropathie sensitivomotrice héréditaire de type I " (French → English) :

TERMINOLOGY
see also In-Context Translations below
neuropathie sensitivomotrice héréditaire de type I
https://browser.ihtsdotools.or (...) (...) [HTML]
HSMN, type I
SNOMEDCT-BE (disorder) / 398040009
SNOMEDCT-BE (disorder) / 398040009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivomotrice héréditaire type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
Refsum's disease
SNOMEDCT-BE (disorder) / 25362006
SNOMEDCT-BE (disorder) / 25362006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [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 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 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 motrice distale héréditaire type Jerash
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 7
https://browser.ihtsdotools.or (...) (...) [HTML]
Distal hereditary motor neuropathy type 7
SNOMEDCT-BE (disorder) / 771081007
SNOMEDCT-BE (disorder) / 771081007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivo-motrice héréditaire type 5
https://browser.ihtsdotools.or (...) (...) [HTML]
Charcot-Marie-Tooth disease, pyramidal features syndrome
SNOMEDCT-BE (disorder) / 771143004
SNOMEDCT-BE (disorder) / 771143004
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivo-motrice héréditaire type Okinawa
https://browser.ihtsdotools.or (...) (...) [HTML]
An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
SNOMEDCT-BE (disorder) / 715665006
SNOMEDCT-BE (disorder) / 715665006
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 : déjerine-sottas    syndrome de roussy-lévy    hypertrophique de l'enfant    neuropathie sensitivo-motrice héréditaire type    neuropathie sensitivo-motrice héréditaire type okinawa    neuropathie sensitivomotrice héréditaire type    neuropathie sensitivomotrice héréditaire de type I    


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neuropathie sensitivomotrice héréditaire de type I

Date index:2021-10-15 -

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