Vertaling van "graefe's disease " (Engels → Frans) :

TERMINOLOGIE

Graefe's disease
progressive external ophthalmoplegia

Graves' disease [ Graves disease | Basedow's disease | Basedow disease | von Basedow disease | Basedow's syndrome | exophthalmic goiter | diffuse toxic goiter | struma exophthalmica | Flajani's disease | Flajani-Basedow syndrome | Parry's disease | Marsh's disease | Begbie's disease ]
maladie de Basedow [ maladie de Graves | goitre exophtalmique | maladie de Parry | maladie de Flajani ]

Paget's disease of the breast | Paget disease of the breast | Paget's disease of the nipple | Paget disease of the nipple | Paget's disease | Paget disease
maladie de Paget du mamelon | maladie de Paget du sein | maladie de Paget mammaire | maladie cutanée de Paget | maladie de Paget

Gilles de la Tourette's syndrome | Gilles de la Tourette's disease | maladie des tics | tic de Guinon | Gilles de la Tourette's disorder | Tourette's disease | Tourette's syndrome | Tourette syndrome | Guinon's disease
syndrome de Gilles de la Tourette | SGT | maladie de Gilles de la Tourette | maladie des tics | syndrome de la Tourette

Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome
syndrome de Sturge-Weber | angiomatose encéphalotrigéminée de Sturge-Weber-Krabbe | angiomatose méningo-oculo-faciale | angiomatose neuro-cutanée | angiomatose neuro-oculo-cutanée | maladie de Sturge-Weber-Krabbe | neuro-ectodermo-dysplasie congénitale | syndrome de Brushfield-Wyatt | syndrome neuro-cutané | syndrome de Parkes-Weber | syndrome de Sturge-Weber-Krabbe | syndrome de Weber-Dimitri

sarcoidosis [ Besnier-Boeck disease | Boeck's disease | Besnier-Boeck sarcoid | sarcoid of Boeck | Schaumann's disease | Schaumann's sarcoid | Schaumann's syndrome ]
sarcoïdose [ maladie de Besnier-Boeck-Schaumann | maladie de Besnier-Böck-Schaumann ]

amyotrophic lateral sclerosis [ ALS | Lou Gehrig's disease | Lou Gehrig disease | Charcot's disease | Charcot disease ]
sclérose latérale amyotrophique [ SLA | maladie de Lou-Gehrig | maladie de Charcot ]

Alzheimer's disease | alzheimer's disease [ AD ]
maladie d'Alzheimer | alzheimer [ MA ]

Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo
ataxie spinocérébelleuse type 38

Care given to improve the quality of life of patients who have a serious or life-threatening disease. The goal of symptom management is to prevent or treat as early as possible the symptoms of a disease, side effects caused by treatment of a disease,
gestion des symptômes

IN-CONTEXT TRANSLATIONS

Graefe zu Baringdorf (Verts/ALE) , draftsman of the opinion of the Committee on Agriculture and Rural Development.– (DE) Madam President, Commissioner Byrne, this being the fifteenth year since cases of the disease first appeared, one might think we had done everything necessary and had got a grip on BSE.
Graefe zu Baringdorf (Verts/ALE), rapporteur pour avis de la commission de l'agriculture et du développement rural. - (DE) Madame la Présidente, Monsieur le Commissaire Byrne, quinze ans après l’apparition des premiers cas d’ESB, l’on pourrait penser que toutes les mesures nécessaires ont été prises et que l’on maîtriserait l’ESB.