Carol Prieto-Morin

Carol Prieto-Morin

UNVERIFIED PROFILE

Are you Carol Prieto-Morin?   Register this Author

Register author
Carol Prieto-Morin

Carol Prieto-Morin

Publications by authors named "Carol Prieto-Morin"

Are you Carol Prieto-Morin?   Register this Author

7Publications

253Reads

31Profile Views

Further refinement of COL4A1 and COL4A2 related cortical malformations.

Eur J Med Genet 2018 Dec 11;61(12):765-772. Epub 2018 Oct 11.

Paris Descartes - Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR 1163, Imagine Institute, Paris, France; Pediatric Neurology, APHP- Necker Enfants Malades Hospital, Paris, France; National Rare Disease Center- Centre de Référence "Déficiences Intellectuelles de Causes Rares", AP-HP, Necker Enfants Malades, 75015, Paris, France. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S17697212173084
Publisher Site
http://dx.doi.org/10.1016/j.ejmg.2018.10.004DOI Listing
December 2018

TREX1 Mutation in Leukodystrophy with Calcifications and Persistent Gadolinium-Enhancement.

Eur Neurol 2017 24;77(3-4):113-114. Epub 2016 Dec 24.

Department of Neurology, Montpellier Universitary Hospital, Montpellier, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000455095DOI Listing
December 2016

CSF1R-related leukoencephalopathy mimicking primary progressive multiple sclerosis.

J Neurol 2016 Sep 17;263(9):1864-5. Epub 2016 Jun 17.

Departement de Neurologie, Hopital Gui de Chauliac, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00415-016-8197-xDOI Listing
September 2016

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.

Brain 2015 Aug 10;138(Pt 8):2347-58. Epub 2015 Jun 10.

1 INSERM UMR 1161, Génétique et Physiopathologie des Maladies Cérébro-vasculaires, Paris, France 2 Université Paris Diderot, Sorbonne Paris Cité, UMR-S1161, Paris, France 5 AP-HP, Groupe Hospitalier Saint-Louis Lariboisière-Fernand-Widal, Service de Génétique Moléculaire Neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), Paris, France

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awv155DOI Listing
August 2015