Ferechte Encha-Razavi
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Explore the profile of Ferechte Encha-Razavi including associated specialties, affiliations and a list of published articles.
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67
Citations
2084
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Recent Articles
1.
Tessier A, Roux N, Boutaud L, Lunel E, Hakkakian L, Parisot M, et al.
Acta Neuropathol Commun
. 2023 Feb;
11(1):29.
PMID: 36803301
Congenital hydrocephalus is a common condition caused by the accumulation of cerebrospinal fluid in the ventricular system. Four major genes are currently known to be causally involved in hydrocephalus, either...
2.
Lubinsky M, Encha-Razavi F
Birth Defects Res
. 2022 Oct;
114(20):1343-1353.
PMID: 36200678
Background: Septo-optic dysplasia (SOD), once a variable triad of septum pellucidum defects (SPDs), optic nerve hypoplasia (ONH), and hypopituitarism, has had multiple findings added, with uncertain causes, definitions, and limits....
3.
Weber M, Jaber D, Encha-Razavi F, Julien E, Grevoul-Fesquet J, Steffann J, et al.
Am J Med Genet A
. 2022 Jun;
188(8):2331-2338.
PMID: 35686685
The recent finding that some patients with fetal akinesia deformation sequence (FADS) carry variants in the TUBB2B gene has prompted us to add to the existing literature a first description...
4.
Gubana F, Christov C, Coste T, Tournier-Lasserve E, Benachi A, Fallet-Bianco C, et al.
Pediatr Dev Pathol
. 2022 Apr;
25(4):435-446.
PMID: 35382634
Background: Increasing number of mutations responsible for vascular lesions, leading to ischemic or hemorrhagic stroke in young adults, has been identified in the recent years. It has been demonstrated in...
5.
Chartier S, Boutaud L, Le Guillou E, Alby C, Billon C, Millischer A, et al.
Birth Defects Res
. 2021 Sep;
113(18):1324-1332.
PMID: 34491000
Background: Neuronal ceroid lipofuscinoses (NCLs) form a clinically and genetically heterogeneous group of inherited neurodegenerative disorders that share common neuropathological features. Although they are the first cause of neurodegenerative disorders...
6.
Tessier A, Boutaud L, Bruel A, Thauvin-Robinet C, Roth P, Malan V, et al.
Clin Genet
. 2020 Sep;
98(6):620-621.
PMID: 32926417
We report two fetal cases carrying a de novo MID1 mutation and presenting with severe hydrothorax, suggesting the expansion of the phenotype of Opitz GBBB syndrome.
7.
Ben Miled S, Loeuillet L, Duong van Huyen J, Bessieres B, Sekour A, Leroy B, et al.
Am J Obstet Gynecol
. 2020 Apr;
223(2):256.e1-256.e9.
PMID: 32283072
Background: Despite undisputable benefits, midtrimester prenatal surgery is not a cure for myelomeningocele (MMC): residual intracranial and motor deficits leading to lifelong handicap question the timing of prenatal surgery. Indeed,...
8.
Sellier Y, Marliot F, Bessieres B, Stirnemann J, Encha-Razavi F, Guilleminot T, et al.
Microorganisms
. 2020 Jan;
8(2).
PMID: 31991822
Background: The understanding of the pathogenesis of cytomegalovirus (CMV)-induced fetal brain lesions is limited. We aimed to quantify adaptive and innate immune cells and CMV-infected cells in fetal brains with...
9.
Hureaux M, Ben Miled S, Chatron N, Coussement A, Bessieres B, Egloff M, et al.
Prenat Diagn
. 2019 Jul;
39(11):1026-1034.
PMID: 31299102
Objective: Neural tube defects (NTDs) are one of the most common congenital anomalies caused by a complex interaction of many genetic and environmental factors. In about 10% of cases, NTDs...
10.
Gardner J, Cushion T, Niotakis G, Olson H, Grant P, Scott R, et al.
Brain Sci
. 2018 Aug;
8(8).
PMID: 30087272
The gene encodes tubulin alpha-1A, a protein that is highly expressed in the fetal brain. Alpha- and beta-tubulin subunits form dimers, which then co-assemble into microtubule polymers: dynamic, scaffold-like structures...