Results 81 to 90 of about 2,873 (179)
Hemimegalencephaly: Prenatal Diagnosis and Outcome
Fetal Diagnosis and Therapy, 2011 Hemimegalencephaly (HME) is a developmental abnormality of the central nervous system (CNS) which may present as either a syndromic or isolated case. Here, we present two cases of early prenatal diagnosis of HME. Prenatal CNS ultrasound and MRI in the first case revealed ventricular asymmetry, midline shift with displacement of the occipital lobe ...
Álvarez, R.M. +6 more
openaire +3 more sources
Pathological differential diagnosis of focal cortical dysplasia type Ⅱ and its mimic lesions
Chinese Journal of Contemporary Neurology and Neurosurgery, 2020 Malformation of cortical development (MCD) accounts for the majority of drug⁃resistant epilepsy, focal cortica ldysplasia type Ⅱ (FCDⅡ) is the most common and most characteristic. It is of great significance to correct diagnosis for FCDⅡ.
Hai-nan LI, Zhi LI
doaj
Neurobiology of Disease, 2014 Spontaneous pacemaker γ-aminobutyric acid (GABA) receptor-mediated synaptic activity (PGA) occurs in a subset of tissue samples from pediatric epilepsy surgery patients.
Carlos Cepeda +6 more
doaj +1 more source
Cell Reports, 2014 De novo copy-number variants (CNVs) can cause neuropsychiatric disease, but the degree to which they occur somatically, and during development, is unknown.
Xuyu Cai +6 more
doaj +1 more source
The ASD Living Biology: from cell proliferation to clinical phenotype. [PDF]
, 2019 Autism spectrum disorder (ASD) has captured the attention of scientists, clinicians and the lay public because of its uncertain origins and striking and unexplained clinical heterogeneity.
Courchesne, Eric +5 more
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Three-dimensional neurorehabilitation: a different perspective [PDF]
, 2015 The authors have narrated their perspective on rehabilitation of neurological disabilities based upon their experiences in three different regions of the globe, hence the word three dimensional .
Mitchell Jenkins, Randolph +1 more
core +1 more source
Klippel-Trenaunay-Weber syndrome with hemimegalencephaly. Report of a case
The Turkish Journal of Pediatrics, 1996 A case of Klippel-Trenaunay-Weber Syndrome (KTWS) in a 2.5-year-old girl with congenital hemihypertrophy, nevus flammeus and liver hemangioma is presented. In addition, this report describes the rare association of hemimegalencephaly with KTWS.
F Alpay +3 more
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Hemimegalencephaly: Seizure outcome in an infant after hemispherectomy [PDF]
, 2018 Isolated hemimegalencephaly (iHME) is a rare form of congenital malformation of cortical development characterized by enlargement of all or part of one cerebral hemisphere.
Abbas, Qalab +2 more
core +1 more source
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis [PDF]
, 2016 BACKGROUND: In frontotemporal dementia (FTD) there is a critical lack in the understanding of biological and molecular mechanisms involved in disease pathogenesis.
Botía, JA +10 more
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A Very Rare Case of Colpocephaly Associated With Trisomy 18
Gynecology Obstetrics & Reproductive Medicine, 2012 We presented a very rare case of colphocephaly which is a term used to describe a congenital abnormal enlargement of the occipital horns of the lateral ventricules associated with normal frontal horns.
Seyfettin Uludağ +3 more
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