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 …

Neurological phenotypes for Down syndrome across the life span

IT Lott - Progress in brain research, 2012 - Elsevier
This chapter reviews the neurological phenotype of Down syndrome (DS) in early
development, childhood, and aging. Neuroanatomic abnormalities in DS are manifested as …

Curcumin and its nano-formulation: the kinetics of tissue distribution and blood–brain barrier penetration

YM Tsai, CF Chien, LC Lin, TH Tsai - International journal of pharmaceutics, 2011 - Elsevier
Curcumin has considerable neuro-protective and anti-cancer properties but is rapidly
eliminated from the body. By optimizing the HPLC method for analysis of curcumin, this …

The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes

J Wegiel, I Kuchna, K Nowicki, H Imaki, J Wegiel… - Acta …, 2010 - Springer
Autism is characterized by a broad spectrum of clinical manifestations including qualitative
impairments in social interactions and communication, and repetitive and stereotyped …

Von Economo neurons in autism: a stereologic study of the frontoinsular cortex in children

M Santos, N Uppal, C Butti, B Wicinski, J Schmeidler… - Brain research, 2011 - Elsevier
The presence of von Economo neurons (VENs) in the frontoinsular cortex (FI) has been
linked to a possible role in the integration of bodily feelings, emotional regulation, and goal …

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy

A Falace, F Filipello, V La Padula, N Vanni… - The American Journal of …, 2010 - cell.com
Idiopathic epilepsies (IEs) are a group of disorders characterized by recurrent seizures in the
absence of detectable brain lesions or metabolic abnormalities. IEs include common …

Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A

E Reinstein, S Frentz, T Morgan… - European Journal of …, 2013 - nature.com
Mutations conferring loss of function at the FLNA (encoding filamin A) locus lead to X-linked
periventricular nodular heterotopia (XL-PH), with seizures constituting the most common …

Epigenetic mechanisms underlying human epileptic disorders and the process of epileptogenesis

IA Qureshi, MF Mehler - Neurobiology of disease, 2010 - Elsevier
The rapidly emerging science of epigenetics and epigenomic medicine promises to reveal
novel insights into the susceptibility to and the onset and progression of epileptic disorders …

A circuitry and biochemical basis for tuberous sclerosis symptoms: from epilepsy to neurocognitive deficits

DM Feliciano, TV Lin, NW Hartman, CM Bartley… - International Journal of …, 2013 - Elsevier
Tuberous sclerosis complex (TSC) is an autosomal dominant monogenetic disorder that is
characterized by the formation of benign tumors in several organs as well as brain …

[图书][B] Epilepsy: the intersection of neurosciences, biology, mathematics, engineering, and physics

I Osorio, HP Zaveri, MG Frei, S Arthurs - 2016 - books.google.com
Integrating the studies of epilepsy, neurosciences, computational neurosciences,
mathematics, physics, engineering, and medicine, this volume provides the first means to a …