Definitions and classification of malformations of cortical development: practical guidelines

M Severino, AF Geraldo, N Utz, D Tortora, I Pogledic… - Brain, 2020 - academic.oup.com
Malformations of cortical development are a group of rare disorders commonly manifesting
with developmental delay, cerebral palsy or seizures. The neurological outcome is …

Cerebral cortex expansion and folding: what have we learned?

V Fernández, C Llinares‐Benadero, V Borrell - The EMBO journal, 2016 - embopress.org
One of the most prominent features of the human brain is the fabulous size of the cerebral
cortex and its intricate folding. Cortical folding takes place during embryonic development …

Nonmicrocephalic infants with congenital Zika syndrome suspected only after neuroimaging evaluation compared with those with microcephaly at birth and postnatally …

M Aragao, AC Holanda… - American Journal …, 2017 - Am Soc Neuroradiology
BACKGROUND AND PURPOSE: Although microcephaly is the most prominent feature of
congenital Zika syndrome, a spectrum with less severe cases is starting to be recognized …

[BOOK][B] Ultrasound of congenital fetal anomalies: differential diagnosis and prognostic indicators

D Paladini, P Volpe - 2018 - taylorfrancis.com
The most frequently asked questions that confront the fetal medicine trainee/expert on a
daily basis are “Is the finding real or merely an artifact?” and “Is the diagnosis correct?” …

Clinical assessment and brain findings in a cohort of mothers, fetuses and infants infected with ZIKA virus

MS Cortes, AM Rivera, M Yepez, CV Guimaraes… - American journal of …, 2018 - Elsevier
Background Congenital Zika virus (ZIKV) infection can be detected in both the presence and
absence of microcephaly and manifests as a number of signs and symptoms that are …

Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathy

N Vegas, M Cavallin, C Maillard, N Boddaert… - Neurology …, 2018 - AAN Enterprises
Objective To provide new insights into the FOXG1-related clinical and imaging phenotypes
and refine the phenotype-genotype correlation in FOXG1 syndrome. Methods We analyzed …

[PDF][PDF] Biallelic mutations in citron kinase link mitotic cytokinesis to human primary microcephaly

H Li, SL Bielas, MS Zaki, S Ismail, D Farfara… - The American Journal of …, 2016 - cell.com
Cell division terminates with cytokinesis and cellular separation. Autosomal-recessive
primary microcephaly (MCPH) is a neurodevelopmental disorder characterized by a …

Development and dysgenesis of the cerebral cortex: malformations of cortical development

C Raybaud, E Widjaja - Neuroimaging Clinics, 2011 - neuroimaging.theclinics.com
The development of the cerebral cortex results from complex and overlapping processes of
cellular proliferation, differentiation, and apoptosis, of migration, and of organization …

[HTML][HTML] Primary autosomal recessive microcephalies and seckel syndrome spectrum disorders–retired chapter, for historical reference only

A Verloes, S Drunat, P Gressens, S Passemard - 2013 - europepmc.org
Primary Autosomal Recessive Microcephalies and Seckel Syndrome Spectrum Disorders –
RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY - Abstract - Europe PMC Sign in …

[HTML][HTML] Morphological and functional aspects of progenitors perturbed in cortical malformations

S Bizzotto, F Francis - Frontiers in cellular neuroscience, 2015 - frontiersin.org
In this review, we discuss molecular and cellular mechanisms important for the function of
neuronal progenitors during development, revealed by their perturbation in different cortical …