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Bourneville disease
Bourneville syndrome
Bourneville-Brissaud disease
Bourneville-Pringle syndrome
Bourneville-Pringle's disease
Dermatosclerosis
Diffuse systemic sclerosis
Disseminated multiple sclerosis
Disseminated sclerosis
Epiloia
Extracapillary glomerulonephritis
Familial centrolobar sclerosis
Familial porphyria cutanea tarda
Focal and segmental hyalinosis
Focal glomerulonephritis
Focal sclerosis
Hide-bound disease
Hidebound disease
Insular sclerosis
MS
Merzbacher-Pelizaeus disease
Minimal change lesion
Multiple sclerosis
PCT
PSS
Pelizaeus-Merzbacher disease
Pelizaeus-Merzbacher sclerosis
Porphyria cutanea tarda
Porphyria cutanea tarda type I
Porphyria cutanea tarda type II
Progressive scleroderma
Progressive systemic sclerosis
Proliferative glomerulonephritis NOS
RP multiple sclerosis
RPMS
Relapsing progressive multiple sclerosis
Relapsing remitting form of multiple sclerosis
SD
SPMS
Scleroderma
Sclerosis
Sclerosis corii
Sclerosis cutanea
Secondary progressive multiple sclerosis
Skin-bound disease
Skinbound disease
Sporadic porphyria cutanea tarda
Systemic scleroderma
Systemic sclerosis
TSC
Tuberous sclerosis
Tuberous sclerosis complex

Traduction de «sclerosis cutanea » (Anglais → Français) :

scleroderma [ SD | hide-bound disease | skin-bound disease | hidebound disease | skinbound disease | dermatosclerosis | sclerosis cutanea | sclerosis corii ]

sclérodermie


multiple sclerosis [ MS | disseminated multiple sclerosis | disseminated sclerosis | focal sclerosis | insular sclerosis ]

sclérose en plaques [ SP,SEP | sclérose multiple | sclérose disséminée ]


multiple sclerosis | MS | disseminated sclerosis | focal sclerosis | insular sclerosis

sclérose en plaques | SP | SEP | sclérose multiple | sclérose multiloculaire


secondary progressive multiple sclerosis | SPMS | relapsing progressive multiple sclerosis | RPMS | relapsing/progressive multiple sclerosis | RP multiple sclerosis

sclérose en plaques progressive secondaire | SPPS | SEPPS | sclérose en plaques secondairement progressive | SEP-SP | sclérose en plaques rémittente secondairement progressive | sclérose en plaques secondaire progressive | SEP-SP | sclérose en plaques rémittente progressive


progressive systemic sclerosis | PSS | systemic scleroderma | progressive scleroderma | systemic sclerosis | diffuse systemic sclerosis

sclérodermie généralisée | sclérodermie systémique | sclérose systémique progressive | sclérodermie diffuse progressive | sclérodermie progressive


familial porphyria cutanea tarda | porphyria cutanea tarda | porphyria cutanea tarda type I | porphyria cutanea tarda type II | sporadic porphyria cutanea tarda | PCT [Abbr.]

porphyrie cutanée symptomatique | porphyrie cutanée tardive | porphyrie cutanée tardive de type I | porphyrie cutanée tardive de type II | porphyrie cutanée tardive familiale | porphyrie cutanée tardive sporadique | PCF [Abbr.] | PCS [Abbr.] | PCT [Abbr.]


Pelizaeus-Merzbacher disease [ Merzbacher-Pelizaeus disease | familial centrolobar sclerosis | Pelizaeus-Merzbacher sclerosis ]

maladie de Pelizaeus-Merzbacher


Bourneville disease | Bourneville syndrome | Bourneville-Brissaud disease | Bourneville-Pringle syndrome | Bourneville-Pringle's disease | epiloia | tuberous sclerosis | tuberous sclerosis complex | TSC [Abbr.]

épiloïa | maladie de Bourneville | maladie de Bourneville-Brissaud | phacomatose de Bourneville | sclérose tubéreuse | sclérose tubéreuse de Bourneville | STB [Abbr.]


Modifiers The following fourth-character subdivisions classify morphological changes and are for use with categories N00-N07. Subdivisions .0-.8 should not normally be used unless these have been specifically identified (e.g. by renal biopsy or autopsy). The three-character categories relate to clinical syndromes. Code Title .0 Minor glomerular abnormality Minimal change lesion .1 Focal and segmental glomerular lesions Focal and segmental:hyalinosis | sclerosis | Focal glomerulonephritis .2 Diffuse membranous glomerulonephritis .3 Diffuse mesangial proliferative glomerulonephritis .4 Diffuse endocapillary proliferative glomerulonephritis ...[+++]

Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les catégories N00-N07 pour classer les modifications morphologiques. Les subdivisions .0-.8 ne doivent être normalement utilisées que s'il y a eu identification précise (par biopsie rénale ou autopsie). Les catégories à trois caractères concernent les syndromes cliniques. Code Titre .0 Anomalies glomérulaires mineures Lésions minimes .1 Lésions glomérulaires segmentaires et focales Glomérulonéphrite focale Hyalinose | Sclérose | segmentaire et focale | .2 Glomérulonéphrite membraneuse diffuse .3 Glomérulonéphrite proliférative mésangiale diffuse ...[+++]


relapsing remitting form of multiple sclerosis

sclérose en plaques évoluant par poussées/rémissions




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Date index: 2023-09-20
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