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Denny-Brown
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie sensitive
Neuropathie sensitivomotrice héréditaire de type I
Neuropathie sensitivomotrice héréditaire type 4
Récessive
Syndrome de Nélaton

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

TERMINOLOGY
see also In-Context Translations below
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]
Neuromyopathie carcinomateuse (C00-C97+) Neuropathie sensitive paranéoplasique [Denny-Brown] (C00-D48+)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Carcinomatous neuromyopathy (C00-C97+) Sensorial paraneoplastic neuropathy [Denny Brown] (C00-D48+)
WORLD HEALTH ORGANIZATION ICD-10: G13.0*
WORLD HEALTH ORGANIZATION ICD-10: G13.0*
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
neuropathie sensitive congénitale avec perte sélective des petites fibres myélinisées
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type V
SNOMEDCT-CA (trouble) / 128206006
SNOMEDCT-CA (trouble) / 128206006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [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]
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]
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 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]
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]


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neuropathie sensitive héréditaire

Date index:2022-05-05 -

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