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AMD
Acid maltase deficiency
Deficiency
Distal
Fazio-Londe
GSD-II
Glycogen storage disease type II
Glycogenosis
Glycogenosis type 0b
Glycogenosis type II
Hers glycogenosis
Hexokinase deficiency
Kugelberg-Welander
PK
Pompe disease
Progressive bulbar palsy of childhood
Pyruvate kinase
Scapuloperoneal form
Spinal muscular atrophy adult form
Touch type
Triose-phosphate isomerase deficiency
Type at speed
Type quickly
Typing at speed

Vertaling van "Glycogenosis type II " (Engels → Nederlands) :

Glycogenosis type II, late onset

laat optredende glycogeenstapelingsziekte type II


Glycogenosis type II, infantile onset

glycogeenstapelingsziekte type II beginnend op zuigelingenleeftijd


acid maltase deficiency | glycogen storage disease type II | glycogenosis type II | Pompe disease | AMD [Abbr.] | GSD-II [Abbr.]

ziekte van Pompe






Atrioventricular block, type I and II Möbitz block, type I and II Second-degree block, type I and II Wenckebach's block

atrioventriculair blok, type I en II | AV-blok, Mobitz type I en II | AV-blok, type Wenckebach | tweedegraads blok, type I en II


Glycogenosis type 0b

spiergebonden en hartgebonden glycogeensynthasedeficiëntie


touch type | type quickly | type at speed | typing at speed

snel typen | typen aan hoge snelheid


Progressive bulbar palsy of childhood [Fazio-Londe] Spinal muscular atrophy:adult form | childhood form, type II | distal | juvenile form, type III [Kugelberg-Welander] | scapuloperoneal form

progressieve bulbairparalyse in kinderjaren [Fazio-Londe] | spinale spieratrofie | distaal | spinale spieratrofie | juveniele vorm, type III [Kugelberg-Welander] | spinale spieratrofie | scapuloperoneale vorm | spinale spieratrofie | van kinderleeftijd, type II | spinale spieratrofie | volwassen vorm


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase




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'Glycogenosis type II' ->

Date index: 2022-12-18
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