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CMT
Charcot-Marie-Tooth disease
Disease Charcot-Marie-Tooth
Déjerine-Sottas
HMSN
Hereditary motor and sensory neuropathy
PMA
Peroneal muscular atrophy

Vertaling van "Hereditary motor and sensory neuropathy " (Engels → Nederlands) :

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]
autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type F
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Hereditary motor and sensory neuropathy
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
hereditaire motorische- en sensorische-neuropathie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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]
erfelijke motorische en sensorische neuropathie met acrodystrofie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
hereditaire motorische en sensorische neuropathie | ziekte van Charcot-Marie-Tooth | HMSN [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
erfelijke motorische en sensorische neuropathie, Okinawa-type
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]
hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : charcot-marie-tooth disease     déjerine-sottas     hereditary motor and sensory neuropathy     peroneal muscular atrophy     Hereditary motor and sensory neuropathy     


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Date index: 2022-07-10
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