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Co-factor supplemented post-mitochondrial fraction
Cofactor supplemented post-mitochondrial fraction
Congenital muscular dystrophy NOS
Disease central core
Hypoparathyroidism
Minicore
Mitochondrial DNA
Mitochondrial myopathy
MtDNA
Multicore
Muscle diease
Myopathy
Myopathy in hyperparathyroidism
Nemaline
Post-mitochondrial fraction
Postmitochondrial supernatant
Pure mitochondrial myopathy
S9
S9 fraction
Supernatant fraction
Thyrotoxic myopathy

Vertaling van "mitochondrial myopathy " (Engels → Nederlands) :



Pure mitochondrial myopathy

zuivere mitochondriale myopathie




A rare genetic mitochondrial DNA-related mitochondrial myopathy disorder with characteristics of slowly progressive muscular weakness (proximal greater than distal), predominantly involving the facial muscles and scapular girdle, associated with insu

myopathie en diabetes mellitus


cofactor supplemented post-mitochondrial fraction | co-factor supplemented post-mitochondrial fraction | S9 [Abbr.] | S9 fraction [Abbr.]

postmitochondriale fractie aangevuld met cofactoren | van co-factor voorziene post-mitochondriale fractie




post-mitochondrial fraction | postmitochondrial supernatant | S9 | S9 fraction | supernatant fraction

postmitochondriale fractie


Myopathy in:hyperparathyroidism (E21.0-E21.3+) | hypoparathyroidism (E20.-+) | Thyrotoxic myopathy (E05.-+)

myopathie bij | hyperparathyroïdie (E21.0-E21.3) | myopathie bij | hypoparathyroïdie (E20.-) | thyrotoxische myopathie (E05.-)




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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Date index: 2023-04-13
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