Boost Your Productivity!Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
AMD
ARMD
Adopted descendant
Adopted family
Adoption of a child
Age-related macular degeneration
Ascending and descending trees
Biological paternity
Centrifugal wallerian degeneration
Climb trees
Corrosion conditions
Corrosion types
Degeneration and oxidising categories
Degeneration and oxidising varieties
Descend trees
Descendant
Descending degeneration
Direct descendant
Legitimate descendant
Lineal descendant
Natural descendant
Relative in the descending line
Senile macular degeneration
Tree climbing

Traduction de «descending degeneration » (Anglais → Néerlandais) :

centrifugal wallerian degeneration | descending degeneration

descenderende degeneratie


descendant | direct descendant | lineal descendant | relative in the descending line

afstammeling | afstammeling in de nederdalende lijn | descendent


descendant [ biological paternity | legitimate descendant | natural descendant ]

afstamming [ biologische vader | legitimatie | natuurlijke afstamming | onwettige afstamming | wettige afstamming | wettiging ]


age-related macular degeneration | senile macular degeneration | AMD [Abbr.] | ARMD [Abbr.]

ouderdomsmaculadegeneratie


descend trees | tree climbing | ascending and descending trees | climb trees

in bomen klimmen


corrosion conditions | degeneration and oxidising varieties | corrosion types | degeneration and oxidising categories

soorten corrosie


A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m

autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type B


A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies

autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type D


Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s

spinocerebellaire ataxie type 28


adoption of a child [ adopted descendant | adopted family ]

adoptie [ adoptiefouders ]


w