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Disease Charcot-Marie-Tooth
Distal axonal painful sensory neuropathy
Déjerine-Sottas

Translation of "distal axonal painful sensory neuropathy " (English → French) :

distal axonal painful sensory neuropathy
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
neuropathie sensitive algique axonale distale
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A rare axonal hereditary motor and sensory neuropathy with characteristics of progressive axonal neuropathy with limb weakness and severe distal sensory loss in all limbs and acrodystrophic changes leading to painless non-healing ulcers, osteomyeliti
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
neuropathie sensitivo-motrice axonale héréditaire avec acrodystrophie
SNOMEDCT-BE (disorder) / 771144005
SNOMEDCT-BE (disorder) / 771144005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
paralysie périodique avec neuropathie motrice distale tardive
SNOMEDCT-BE (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. / 774154008
SNOMEDCT-BE (disorder) / 774154008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare hereditary motor and sensory neuropathy disorder with characteristics of the typical CMT phenotype (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante type F
SNOMEDCT-BE (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend / 770759001
SNOMEDCT-BE (disorder) / 770759001
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


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'distal axonal painful sensory neuropathy'

Date index:2021-07-25 -

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