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AACPDM
American Academy for Cerebral Palsy
Athlete with cerebral palsy
CP athlete
Cerebral lymphoma
Cerebral palsy athlete
Cerebral porosis
Cerebral proton MR spectroscopy
Cerebral proton MRS
Cerebral proton magnetic resonance spectroscopy
Cerebral-palsied athlete
Congenital cerebral porosis
General cerebral syndrome
General posttraumatic cerebral syndrome
Perencephalia
Perencephaly
Porencephaly
Primitive cerebral lymphoma

Vertaling van "cerebral porosis " (Engels → Frans) :

cerebral porosis

état de fromage de Gruyère | porose cérébrale


porencephaly [ perencephalia | perencephaly | cerebral porosis ]

porencéphalie


Congenital cerebral porosis

porencéphalie congénitale


in vivo cerebral proton magnetic resonance spectroscopy | cerebral proton magnetic resonance spectroscopy | cerebral proton MR spectroscopy | cerebral proton MRS

spectroscopie de résonance magnétique cérébrale du proton in vivo | spectroscopie de résonance magnétique cérébrale du proton | SRM cérébrale du proton | SRM cérébrale | spectroscopie cérébrale du proton | spectroscopie de résonance magnétique protonique du cerveau | SRM protonique du cerveau


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 ]


American Academy for Cerebral Palsy and Developmental Medicine [ AACPDM | American Academy for Cerebral Palsy ]

American Academy for Cerebral Palsy and Developmental Medicine [ AACPDM | American Academy for Cerebral Palsy ]


cerebral lymphoma | primitive cerebral lymphoma

lymphome cérébral | lymphome primitif cérébral


general cerebral syndrome | general posttraumatic cerebral syndrome

syndrome cérébral général | syndrome cérébral général posttraumatique


A rare non-syndromic cerebellar malformation with characteristics of loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (normal cerebral hemispheres, fourth ventricle, pons, medulla and m

hypoplasie isolée unilatérale des hémisphères cérébelleux


Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,

ataxie spinocérébelleuse type 31




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'cerebral porosis' ->

Date index: 2021-11-11
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