Boost Your Productivity!Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!

Traduction de «Idiopathic progressive neuropathy » (Anglais → Français) :

Idiopathic progressive neuropathy

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Neuropathie progressive idiopathique

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Bell palsy [ Bell's palsy | idiopathic facial paralysis | herpetic facial paralysis | acute idiopathic facial neuropathy ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

paralysie de Bell [ maladie de Bell | paralysie faciale a frigore | paralysie faciale idiopathique | paralysie faciale essentielle | paralysie faciale périphérique ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

polyradiculonévrite aiguë | polyradiculonévrite aiguë inflammatoire | polyradiculonévrite curable | syndrome de Guillain-Barré

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

idiopathic atrophoderma Pasini-Pierini | progressive idiopathic atrophoderma

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

atrophodermie progressive idiopathique | atrophodermie progressive idiopathique de Pasini-Pierini

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

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

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

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante C

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

progressive muscular dystrophy | Erb-Landouzy disease | Erb's disease | idiopathic muscular atrophy | myodystrophia

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

Other hereditary and idiopathic neuropathies

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Autres neuropathies héréditaires et idiopathiques

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]