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Alcoholic cerebellar ataxia
Angioid streaks
Athlete with cerebral palsy
Axon reaction
Axonal degeneration
Axonal reaction
CP athlete
Cerebral degeneration
Cerebral degeneration in Hunter disease
Cerebral palsy athlete
Cerebral-palsied athlete
Cyst
Degeneration
Dementia in cerebral lipidosis
Drusen
Dysfunction of autonomic nervous system due to alcohol
Encephalopathy
Epilepsy
Hepatolenticular degeneration
Hole
Hypercalcaemia
Intoxications
Mucoid degeneration
Multiple sclerosis
Myxoid degeneration
Myxomatous degeneration
Neurosyphilis
Niacin deficiency
Nissl degeneration
Of macula
Pellagra
Polyarteritis nodosa
Puckering
Retrograde degeneration
Systemic lupus erythematosus
Vitamin B12 deficiency

Translation of "cerebral degeneration " (English → French) :

Cerebral degeneration

maladie dégénérative du cerveau


Cerebral degeneration in Hunter disease

dégénérescence cérébrale dans la maladie de Hunter


Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol

Ataxie cérébelleuse | Dégénérescence cérébelleuse | Dégénérescence cérébrale | Dysautonomie | Encéphalopathie | alcoolique


mucoid degeneration | myxoid degeneration | myxomatous degeneration

dégénérescence mucoïde | dégénérescence myxomateuse


axon reaction [ axonal reaction | axonal degeneration | Nissl degeneration | retrograde degeneration ]

dégénérescence axonale


myxomatous degeneration [ mucoid degeneration | myxoid degeneration ]

dégénérescence myxomateuse


Dementia in:cerebral lipidosis (E75.-+) | epilepsy (G40.-+) | hepatolenticular degeneration (E83.0+) | hypercalcaemia (E83.5+) | hypothyroidism, acquired (E01.-+, E03.-+) | intoxications (T36-T65+) | multiple sclerosis (G35+) | neurosyphilis (A52.1+) | niacin deficiency [pellagra] (E52+) | polyarteritis nodosa (M30.0+) | systemic lupus erythematosus (M32.-+) | trypanosomiasis (B56.-+, B57.-+) | vitamin B12 deficiency (E53.8+)

Démence au cours de:carence en:acide nicotinique [pellagre] (E52+) | vitamine B12 (E53.8+) | dégénérescence hépatolenticulaire (E83.0+) | épilepsie (G40.-+) | hypercalcémie (E83.5+) | hypothyroïdie acquise (E01.-+, E03.-+) | intoxications (T36-T65+) | lipidose cérébrale (E75.-+) | lupus érythémateux disséminé (M32.-+) | neurosyphilis (A52.1+) | périartérite noueuse (M30.0+) | sclérose en plaques (G35+) | trypanosomiase (B56.-+, B57.-+)


athlete with cerebral palsy [ cerebral-palsied athlete | cerebral palsy athlete | CP athlete ]

athlète atteint de paralysie cérébrale [ athlète atteinte de paralysie cérébrale | athlète infirme moteur cérébral | athlète IMC ]


Angioid streaks | Cyst | Drusen (degenerative) | Hole | Puckering | of macula | Kuhnt-Junius degeneration Senile macular degeneration (atrophic)(exudative) Toxic maculopathy

Dégénérescence (de):Junius-Kuhnt | maculaire sénile (atrophique) (exsudative) | Druses (dégénératives) | Kyste | Plis | Stries angioïdes | Trou | de la macula | Maculopathie toxique


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

ataxie spinocérébelleuse type 28




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'cerebral degeneration' ->

Date index: 2020-12-12
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