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Above mentioned
Aran-Duchenne disease
Autonomic neuropathy
Charcot-Marie-Tooth disease
Choroideremia
Cruveilhier disease
DRPLA
Dentato-rubro-pallidolusian atrophy
Dentatorubral pallidolusyian atrophy
Dentatorubral-pallidoluysian atrophy
Dentatorubropallidoluysian atrophy
Diabetic acidosis
Diabetic amyotrophy
Diabetic cataract
Diabetic coma with or without ketoacidosis
Diabetic gangrene
Duchenne disease
Duchenne dystrophy
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne-Griesinger disease
Erb atrophy
Erb dystrophy
Hyperglycaemic coma NOS
Hyperosmolar coma
Hypoglycaemic coma
Infantile spinal muscular atrophy
Kennedy disease
Kennedy's disease
Ketoacidosis
Leber's disease
Leber's hereditary optic atrophy
Leber's optic atrophy
Leber's optic neuropathy
Mentioned above
Mentioned hereinbefore
Mononeuropathy
PMA
Peripheral angiopathy+
Peroneal muscular atrophy
Polyneuropathy
Progressive chorioretinal degeneration
Progressive choroidal atrophy
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive neuromuscular atrophy
Progressive spinal muscular atrophy
Progressive tapetochoroidal atrophy
Progressive tapetochoroidal dystrophy
Retinopathy
SBMA
SMA
SMA I
SPMA
Severe infantile spinal muscular atrophy
Spinal and bulbar muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Spinobulbar muscular atrophy
Tapetochoroidal dystrophy
Ulcer
Werdnig-Hoffman disease
Without mention of coma
X-linked spinal and bulbar muscular atrophy
Zimmerlin atrophy

Vertaling van "mention atrophied " (Engels → Frans) :

TERMINOLOGIE
dentatorubral pallidolusyian atrophy | DRPLA | dentato-rubro-pallidolusian atrophy | dentatorubropallidoluysian atrophy | dentatorubral-pallidoluysian atrophy

atrophie dentaturo-rubro-pallido-luysienne | atrophie dentato-rubro-pallydoluysienne | dégénérescence dentato-rubro-pallidoluysienne | atrophie dentato-rubro-pallidoluysienne | DRPLA | syndrome Haw river


spinal and bulbar muscular atrophy | SBMA | Kennedy disease | X-linked spinal and bulbar muscular atrophy | spinobulbar muscular atrophy | Kennedy's disease

maladie de Kennedy | atrophie musculaire spinale et bulbaire | atrophie spinale bulbo-musculaire | amyotrophie spinobulbaire | SBMA


Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne


infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

amyotrophie spinale infantile sévère | amyotrophie spinale progressive de type I | atrophie spinale progressive infantile | maladie de Werdnig-Hoffmann | syndrome de Werdnig-Hoffmann


above mentioned | mentioned above | mentioned hereinbefore

mentionné ci-dessus | précité | susmentionné


Duchenne muscular dystrophy [ Duchenne type muscular dystrophy | Duchenne dystrophy | Duchenne disease | Erb dystrophy | Duchenne-Griesinger disease | Zimmerlin atrophy | Erb atrophy ]

maladie de Duchenne de Boulogne


Charcot-Marie-Tooth disease | peroneal muscular atrophy | progressive neuromuscular atrophy

maladie de Charcot-Marie | syndrome de Charcot-Marie | atrophie de Charcot-Marie | atrophie péronière | amyotrophie de Charcot-Marie-Tooth


choroideremia [ tapetochoroidal dystrophy | progressive tapetochoroidal dystrophy | progressive choroidal atrophy | progressive tapetochoroidal atrophy | progressive chorioretinal degeneration ]

choroïdérémie [ dégénérescence chorio-rétinienne progressive ]


Leber's hereditary optic atrophy [ Leber's optic atrophy | Leber's disease | Leber's optic neuropathy ]

maladie de Leber [ atrophie optique de Leber | atrophie optique héréditaire et familiale ]


Modifiers The following fourth-character subdivisions are for use with categories E10-E14: Code Title .0 With coma Diabetic:coma with or without ketoacidosis | hyperosmolar coma | hypoglycaemic coma | Hyperglycaemic coma NOS .1 With ketoacidosis Diabetic:acidosis | ketoacidosis | without mention of coma | .2+ With renal complications Diabetic nephropathy (N08.3*) Intracapillary glomerulonephrosis (N08.3*) Kimmelstiel-Wilson syndrome (N08.3*) .3+ With ophthalmic complications Diabetic:cataract (H28.0*) | retinopathy (H36.0*) | .4+ With neurological complications Diabetic:amyotrophy (G73.0*) | autonomic neuropathy (G99.0*) | mononeuropathy ...[+++]

Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les rubriques E10-E14: Code Titre .0 Avec coma Coma:diabétique, avec ou sans acidocétose:hyperglycémique | hyperosmolaire | hyperglycémique SAI | .1 Avec acidocétose Acidocétose | Acidose | diabétique, sans mention de coma | .2+ Avec complications rénales Glomérulonéphrite intracapillaire (N08.3*) Néphropathie diabétique (N08.3*) Syndrome de Kimmelstiel-Wilson (N08.3*) .3+ Avec complications oculaires Cataracte (H28.0*) | Rétinopathie (H36.0*) | diabétique | .4+ Avec complications neurologiques Amyotrophie ...[+++]
IN-CONTEXT TRANSLATIONS
Biochemist Árpád Pousztai, after putting rats on a 10-day diet of genetically modified potatoes, discovered immune system defects, abnormal stimulations of the pancreas, the intestine, the prostate — my colleague will be happy to hear that one — and testicles— and maybe that will worry him even further — not to mention atrophied liver and brain development.

Le biochimiste Árpád Pousztai, après les avoir soumis pendant 10 jours à un régime de pommes de terre transgéniques, a découvert chez des rats des dérèglements du système immunitaire, des stimulations anormales du pancréas, de l'intestin, de la prostate — mon collègue va être content de savoir cela — et des testicules — cela le rendra peut-être inquiet aussi —, des atrophies du foie et du développement du cerveau.




Anderen hebben gezocht naar : aran-duchenne disease     charcot-marie-tooth disease     cruveilhier disease     diabetic acidosis     diabetic amyotrophy     diabetic cataract     diabetic gangrene     duchenne disease     duchenne dystrophy     duchenne muscular dystrophy     duchenne type muscular dystrophy     duchenne-griesinger disease     erb atrophy     erb dystrophy     hyperglycaemic coma nos     kennedy disease     kennedy's disease     leber's disease     leber's hereditary optic atrophy     leber's optic atrophy     leber's optic neuropathy     werdnig-hoffman disease     zimmerlin atrophy     above mentioned     autonomic neuropathy     choroideremia     dentatorubral pallidolusyian atrophy     hyperosmolar coma     hypoglycaemic coma     infantile spinal muscular atrophy     ketoacidosis     mentioned above     mentioned hereinbefore     mononeuropathy     peripheral angiopathy+     peroneal muscular atrophy     progressive chorioretinal degeneration     progressive choroidal atrophy     progressive muscular atrophy     progressive muscular atrophy of infancy     progressive neuromuscular atrophy     progressive spinal muscular atrophy     progressive tapetochoroidal atrophy     progressive tapetochoroidal dystrophy     retinopathy     severe infantile spinal muscular atrophy     spinal and bulbar muscular atrophy     spinal muscular atrophy     spinal muscular atrophy type     spinal progressive muscular atrophy     spinobulbar muscular atrophy     tapetochoroidal dystrophy     without mention of coma     mention atrophied     


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Date index: 2025-03-08
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