Kolexia
Garel Catherine
Radio-diagnostic
Hôpital Armand Trousseau
Paris, France
174 Activités
0 Followers

Scientifique
Digital
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Expertise
Sujets de recherche
{{person.topmesh1.name}} Malformations du système nerveux Maladies foetales Agénésie du corps calleux Kystes Malformations multiples Dysraphie spinale Encéphalopathies Myéloméningocèle Malformations

Industries

Canon Medical Systems France
1 collaboration(s)
Dernière en 2022
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Dernières activités

Subdural hemorrhages and severe retinal hemorrhages in a short fall with a rotational component.
Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus   17 janvier 2024
Prenatal diagnosis of pontocerebellar hypoplasia with postnatal follow-up.
Prenatal diagnosis   02 janvier 2024
Loss of function variants in ZEB1 cause dominant agenesis of the corpus callosum with incomplete penetrance
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Prenatal exome sequencing in corpus callosum anomalies: lessons from a cohort of 209 fetuses
Abstracts from the 56th European Society of Human Genetics (ESHG) Conference   01 janvier 2024
Reversed cortico-medullary differentiation in the fetal and neonatal kidneys: an indicator of poor prognosis?
Pediatric radiology   27 décembre 2023
Further characterisation of -related disorders in females due to inherited or de novo variants.
Journal of medical genetics   25 octobre 2023
Loss-of-function variants in cause dominant anomalies of the corpus callosum with favourable cognitive prognosis.
Journal of medical genetics   19 octobre 2023
Prenatal imaging of the normal and abnormal spinal cord: recommendations from the Fetal Task Force of the European Society of Paediatric Radiology (ESPR) and the European Society of Neuroradiology (ESNR) Pediatric Neuroradiology Committee.
Pediatric radiology   07 octobre 2023
Spectrum of brain malformations in fetuses with mild tubulinopathy.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology   05 juin 2023
First reports of fetal SMARCC1 related hydrocephalus.
European journal of medical genetics   05 juin 2023