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Autosomaal dominante limb-girdle-spierdystrofie type 1A
Autosomaal dominante limb-girdle-spierdystrofie type 1B
Autosomaal dominante limb-girdle-spierdystrofie type 1F
Becker
Benigne
Benigne scapuloperoneaal met vroege contracturen
Central-core-disease
Congenitale spierdystrofie
Distaal
Duchenne
Duchenne spierdystrofie
Emery-Dreifuss
Ernstig
Facioscapulohumeraal
Fibre-type disproportion
Minicore disease
Multicore disease
Myopathie
Myotubulair
NNO
Nemaline lichaampjes
Oculair
Oculofaryngeaal
Progressieve spierdystrofie
Pseudohypertrofische musculaire dystrofie
Scapuloperoneaal
Schouder- en bekkengordel
Spierdystrofie

Vertaling van "Spierdystrofie " (Nederlands → Engels) :

TERMINOLOGIE
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://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://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Duchenne spierdystrofie | pseudohypertrofische musculaire dystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
spierdystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
muscular dystrophy | MD [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
spierdystrofie
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Muscular dystrophy
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
progressieve spierdystrofie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
progressive muscular dystrophy
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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://terminologie.nictiz.nl (...) (...) [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://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
autosomaal dominante limb-girdle-spierdystrofie type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Autosomal dominant limb girdle muscular dystrophy type 1B
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
autosomaal dominante limb-girdle-spierdystrofie type 1F
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Autosomal dominant limb girdle muscular dystrophy type 1F
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
autosomaal dominante limb-girdle-spierdystrofie type 1A
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Autosomal dominant limb girdle muscular dystrophy type 1A
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
IN-CONTEXT TRANSLATIONS
Overzicht van Europese proefreferentienetwerken inzake zeldzame ziekten · Dyscerne: Europees netwerk van referentiecentra voor dysmorfologie (European Network of Centres of Reference for Dysmorphology) · ECORN CF: Europees netwerk van referentiecentra voor taaislijmziekte (European Centres of Reference Network for Cystic Fibrosis) · PAAIR: Internationaal register van patiëntenverenigingen en Alpha1 (Patient Associations and Alpha1 International Registry) · EPNET: Europees porfyrienetwerk · EN-RBD: Europees Netwerk voor zeldzame bloedaandoeningen, netwerk van Hodgkin lymfoom bij kinderen (European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network) · NEUROPED: Europees netwerk voor zeldzame neurologische aandoeningen bi ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2009-06-07]
List of pilot European Reference Networks for Rare Diseases · Dyscerne: European Network of Centres of Reference for Dysmorphology · ECORN CF: European Centres of Reference Network for Cystic Fibrosis · PAAIR: Patient Associations and Alpha1 International Registry, · EPNET European Porphyria Network, · EN-RBD European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network · NEUROPED: European Network of Reference for Rare Paediatric Neurological Diseases · EURO HISTIO NET: A reference network for Langerhans cell histiocytosis and associated syndrome in EU · TAG: Together Against Genodermatoses · CARE NMD: Dissemination and Implementation of the Standards of Care for Duchene muscular Dyst ...[+++]
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2009-06-07]
https://eur-lex.europa.eu/lega (...) [HTML] [2009-06-07]
Overzicht van Europese proefreferentienetwerken inzake zeldzame ziekten · Dyscerne: Europees netwerk van referentiecentra voor dysmorfologie (European Network of Centres of Reference for Dysmorphology) · ECORN CF: Europees netwerk van referentiecentra voor taaislijmziekte (European Centres of Reference Network for Cystic Fibrosis) · PAAIR: Internationaal register van patiëntenverenigingen en Alpha1 (Patient Associations and Alpha1 International Registry) · EPNET: Europees porfyrienetwerk · EN-RBD: Europees Netwerk voor zeldzame bloedaandoeningen, netwerk van Hodgkin lymfoom bij kinderen (European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network) · NEUROPED: Europees netwerk voor zeldzame neurologische aandoeningen bi ...[+++]
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2009-06-07]
List of pilot European Reference Networks for Rare Diseases · Dyscerne: European Network of Centres of Reference for Dysmorphology · ECORN CF: European Centres of Reference Network for Cystic Fibrosis · PAAIR: Patient Associations and Alpha1 International Registry, · EPNET European Porphyria Network, · EN-RBD European Network of Rare Bleeding Disorders, Paediatric Hodgkins Lymphoma Network · NEUROPED: European Network of Reference for Rare Paediatric Neurological Diseases · EURO HISTIO NET: A reference network for Langerhans cell histiocytosis and associated syndrome in EU · TAG: Together Against Genodermatoses · CARE NMD: Dissemination and Implementation of the Standards of Care for Duchene muscular Dyst ...[+++]
http://eur-lex.europa.eu/legal (...) (...) [HTML] [2009-06-07]
http://eur-lex.europa.eu/legal (...) [HTML] [2009-06-07]


Anderen hebben gezocht naar : becker     duchenne     duchenne spierdystrofie     emery-dreifuss     benigne     benigne scapuloperoneaal met vroege contracturen     central-core-disease     congenitale spierdystrofie     distaal     ernstig     facioscapulohumeraal     fibre-type disproportion     minicore disease     multicore disease     myopathie     myotubulair     nemaline lichaampjes     oculair     oculofaryngeaal     progressieve spierdystrofie     pseudohypertrofische musculaire dystrofie     scapuloperoneaal     en bekkengordel     spierdystrofie     Spierdystrofie     


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