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AIDP
Acute autoimmune neuropathy
Acute idiopathic polyneuritis
Acute idiopathic polyradiculoneuritis
Acute inflammatory demyelinating polyneuropathy
Acute inflammatory polyneuropathy
Acute inflammatory polyradiculoneuropathy
GBS
Guillain-Barré syndrome
Guillain-Barré-Strohl syndrome
Hereditary and idiopathic neuropathy
Idiopathic atrophoderma Pasini-Pierini
Idiopathic progressive neuropathy
Infectious polyneuritis
LGBS
Landry's paralysis
Landry-Guillain-Barré Syndrome
Other hereditary and idiopathic neuropathies
Progressive idiopathic atrophoderma

Traduction de «idiopathic progressive neuropathy » (Anglais → Néerlandais) :

Idiopathic progressive neuropathy

idiopathische progressieve neuropathie


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.]

acute inflammatoire demyeliniserende polyradiculoneuropathie


idiopathic atrophoderma Pasini-Pierini | progressive idiopathic atrophoderma

progessieve idiopathische huidatrofie | syndroom van Pasini-Pierini


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.

periodieke verlamming met distale motorneuropathie met latere aanvang


A subtype of autosomal dominant Charcot-Marie-Tooth disease type 2 with characteristics of late adult-onset (50-60 years of age) of slowly progressive, axonal, peripheral sensorimotor neuropathy resulting in distal upper limb and proximal and distal

autosomaal dominante hereditaire motorische en sensorische neuropathie type 2U


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

autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type C


Other hereditary and idiopathic neuropathies

overige gespecificeerde hereditaire- en idiopathische neuropathieën


Hereditary and idiopathic neuropathy

hereditaire en idiopathische neuropathie


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