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Becker
Benign
Benign scapuloperoneal with early contractures
Congenital muscular dystrophy NOS
Disease central core
Distal
Duchenne
Eichhorst type
Emery-Dreifuss
Facioscapulohumeral
Hereditary progressive muscular dystrophy
Limb-girdle
Minicore
Multicore
Muscular dystrophy
Nemaline
Ocular
Oculopharyngeal
Progressive muscular dystrophy
Progressive muscular dystrophy Eichhorst
Progressive muscular dystrophy of pelvic girdle
Scapuloperoneal
Severe

Vertaling van "Progressive muscular dystrophy " (Engels → Nederlands) :

progressive muscular dystrophy of pelvic girdle
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
syndroom van Duchenne-van Leyden
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
progressive muscular dystrophy
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
progressieve spierdystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A rare progressive muscular dystrophy characterized by an adult-onset scapulo-axio-peroneal myopathy. Clinical presentation includes shoulder girdle atrophy, scapular winging, axial muscular atrophy of postural muscles combined with a generalized hyp
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
X-gebonden myopathie met posturale spieratrofie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Eichhorst type | progressive muscular dystrophy | progressive muscular dystrophy Eichhorst
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
type van Eichhorst
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Hereditary progressive muscular dystrophy
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
hereditaire progressieve spierdystrofie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Syndrome that is characterized by total color blindness caused by progressive cone dystrophy, degenerative liver disease, and endocrine dysfunction (hypothyroidism, diabetes, repeated abortions or infertility). It has been described in six females fr
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
retinohepato-endocrinologisch syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Muscular dystrophy
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
spierdystrofie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Muscular dystrophy:autosomal recessive, childhood type, resembling Duchenne or Becker | benign [Becker] | benign scapuloperoneal with early contractures [Emery-Dreifuss] | distal | facioscapulohumeral | limb-girdle | ocular | oculopharyngeal | scapuloperoneal | severe [Duchenne]
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
spierdystrofie | autosomaal recessief, op kinderleeftijd, gelijkend op Duchenne of Becker | spierdystrofie | benigne [Becker] | spierdystrofie | benigne scapuloperoneaal met vroege contracturen [Emery-Dreifuss] | spierdystrofie | distaal | spierdystrofie | ernstig [Duchenne] | spierdystrofie | facioscapulohumeraal | spierdystrofie | schouder- en bekkengordel | spierdystrofie | oculair | spierdystrofie | oculofaryngeaal | spierdystrofie | scapuloperoneaal
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : becker     congenital muscular dystrophy nos     disease central core     duchenne     eichhorst type     emery-dreifuss     fibre-type disproportion myopathy myotubular     hereditary progressive muscular dystrophy     muscular dystrophy     benign     benign scapuloperoneal with early contractures     distal     facioscapulohumeral     limb-girdle     minicore     multicore     nemaline     ocular     oculopharyngeal     progressive muscular dystrophy     progressive muscular dystrophy eichhorst     scapuloperoneal     severe     Progressive muscular dystrophy     


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Date index: 2021-09-18
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