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AIDP
Acute autoimmune neuropathy
Acute febrile polyneuritis
Acute idiopathic polyneuritis
Acute idiopathic polyradiculoneuritis
Acute inflammatory demyelinating polyneuropathy
Acute inflammatory polyneuropathy
Acute inflammatory polyradiculoneuropathy
Alcoholic neuropathy
Alcoholic polyneurites
Alcoholic polyneuritis
Alcoholic polyneuropathy
Erythrooedema polyneuritis
GBS
Guillain-Barré syndrome
Guillain-Barré-Strohl syndrome
Infectious polyneuritis
LGBS
Landry's paralysis
Landry-Guillain-Barré Syndrome
Landry-Guillain-Barré syndrome
Multiple neuritis
Polyneuritis
Polyneuritis potatorum
Polyneuropathy
Potatorum polyneuritis

Traduction de «polyneuritis nos » (Anglais → Français) :

acute autoimmune neuropathy | acute idiopathic polyneuritis | acute idiopathic polyradiculoneuritis | acute inflammatory demyelinating polyneuropathy | acute inflammatory demyelinating polyradiculoneuropathy | acute inflammatory polyneuropathy | acute inflammatory polyradiculoneuropathy | Guillain-Barré syndrome | Guillain-Barré-Strohl syndrome | infectious polyneuritis | Landry-Guillain-Barré Syndrome | Landry's paralysis | AIDP [Abbr.] | GBS [Abbr.] | LGBS [Abbr.]

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


alcoholic polyneuritis | potatorum polyneuritis

polynévrite alcoolique




acute idiopathic polyneuritis | Guillain-Barré syndrome | Landry-Guillain-Barré syndrome | acute febrile polyneuritis

syndrome de Guillain-Barré | SGB | syndrome de Guillain et Barré | SGB | polyradiculonévrite curable | polyradiculonévrite aiguë | syndrome de Landry-Guillain-Barré | plexite aiguë






polyneuropathy | polyneuritis | multiple neuritis

polyneuropathie | neuropathie multiple | polynévrite


alcoholic polyneurites [ alcoholic polyneuropathy | alcoholic neuropathy | polyneuritis potatorum ]

polynévrite alcoolique [ polyneuritis potatorum ]


An X-linked disorder of purine metabolism comprised of two forms: an early-onset severe form with characteristics of gout, urolithiasis, and neurodevelopmental anomalies (severe PRPP synthetase superactivity) and a mild late-onset form with no neurol

hyperactivité de la phosphoribosylpyrophosphate synthétase


A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g

fente labiale médiane supérieure et inférieure, forme familiale


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