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Becker
Benign
Benign scapuloperoneal with early contractures
Congenital muscular dystrophy NOS
DMD
Disease central core
Distal
Duchenne
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Eichhorst type
Emery-Dreifuss
Encephalopathy NOS
Exertional periodontic dystrophy
Facioscapulohumeral
Fulminant
Hepatic coma NOS
Hepatitis acute
Inner tube
Limb-girdle
Malignant
Meryon's disease
Minicore
Multicore
Muscular dystrophy - Duchenne type
Nemaline
Ocular
Oculopharyngeal
Pneumatic tyre
Progressive muscular dystrophy
Progressive muscular dystrophy Eichhorst
Pseudohypertrophic muscular dystrophy
Scapuloperoneal
Severe
Stress dystrophy of the marginal periodontium
Tire industry
Tyre
Tyre industry
Tyres

Vertaling van "dystrophy with inner " (Engels → Nederlands) :

Retinal dystrophy with inner nuclear layer and ganglion cell anomalies

retinale dystrofie met binnenste retinale disfunctie en ganglioncelanomalieën


Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]

Duchenne spierdystrofie | pseudohypertrofische musculaire dystrofie


Eichhorst type | progressive muscular dystrophy | progressive muscular dystrophy Eichhorst

type van Eichhorst


exertional periodontic dystrophy | stress dystrophy of the marginal periodontium

dystrophia diffusa | paradentitis dystrophicans complicata | parodontitis dystrophicans | parodontopathia mixta


A rare genetic multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing

branchio-otisch syndroom


A subtype of junctional epidermolysis bullosa (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge

junctionele epidermolysis bullosa, niet-Herlitz-type


hepatic:coma NOS | encephalopathy NOS | hepatitis:acute | fulminant | malignant | NEC, with hepatic failure | liver (cell) necrosis with hepatic failure yellow liver atrophy or dystrophy

gele leveratrofie of leverdystrofie | hepatisch(e) | coma NNO | hepatisch(e) | encefalopathie NNO | hepatitis | fulminant | NEC, met leverinsufficiëntie | hepatitis | maligne | NEC, met leverinsufficiëntie | lever(cel)necrose met leverinsufficiëntie


pneumatic tyre [ inner tube | tyre | Tyres(ECLAS) | Tyre industry(STW) | tire industry(UNBIS) ]

luchtband [ luchtkamer ]


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]

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


Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

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


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