Results 61 to 70 of about 4,566 (168)
Language Disorder and Polymicrogyria
Pediatric Neurology Briefs, 2008 The co-occurrence of developmental language disorder and reading impairment in members of three families with perisylvian polymicrogyria is reported from the State University of Campinas, and University of Sao Paulo, Brazil.
J Gordon Millichap
doaj +1 more source
Epilepsia Open, Volume 11, Issue 2, Page 592-604, April 2026.Abstract Objective To investigate a recently developed MRI technique for mapping the Mean Diffusivity of Tissue (MDT), which improves diffusion MRI imaging of the cerebral cortex by reducing partial volume effects from cerebrospinal fluid (CSF). As cortical lesions are common in patients with focal epilepsy, we explored the clinical value of MDT ...
Irena Grubor +5 more
wiley +1 more source
Developmental Language Disorder and Polymicrogyria
Pediatric Neurology Briefs, 2002 Neuroimaging studies were conducted in 15 children (11 boys), ages 4 to 14 years, with primary complaint of language delay, in a study at the Department of Neurology, University of Campinas, Brazil.
J Gordon Millichap
doaj +1 more source
International Journal of Developmental Neuroscience, Volume 86, Issue 2, April 2026.Children with congenital Zika syndrome followed at a neurorehabilitation centre demonstrated severe neurological impairment characterized by microcephaly, cortical malformations, intracranial calcifications and multifocal epileptiform activity. Integrated clinical, neuroimaging and video‐electroencephalographic (EEG) findings highlight the extensive ...
Adilina Soares Romeiro Rodrigues +5 more
wiley +1 more source
Анналы клинической и экспериментальной неврологии, 2017 Clinical and morphological correlations in the group of corticaldysplasias accompanied by the development of an epilepticsyndrome were performed based on 50 autopsies.
O. A. Milovanova +6 more
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Clinical Genetics, Volume 109, Issue 4, Page 788-795, April 2026.We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil +9 more
wiley +1 more source
Polymicrogyria in Fetal Alcohol Syndrome
Neuropediatrics, 2009 AbstractBACKGROUND: Intrauterine exposure to alcohol may result in a distinct pattern of craniofacial abnormalities and central nervous system dysfunction, designated fetal alcohol syndrome (FAS). The spectrum of malformations of the brain associated with maternal alcohol abuse during pregnancy is much broader than the relatively uniform clinical ...
Reinhardt, Konstanze +4 more
openaire +3 more sources
Developmental Medicine &Child Neurology, Volume 68, Issue 4, Page 477-488, April 2026.Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.70070 Abstract Aim To identify the outcomes and standardized tools used to measure changes following telehealth‐delivered physical therapy interventions in children and young people with cerebral palsy, within the framework of the International Classification of Functioning ...
Isabella S. Christovão +6 more
wiley +1 more source
The α-Tubulin gene TUBA1A in Brain Development: A Key Ingredient in the Neuronal Isotype Blend
Journal of Developmental Biology, 2017 Microtubules are dynamic cytoskeletal polymers that mediate numerous, essential functions such as axon and dendrite growth and neuron migration throughout brain development.
Jayne Aiken +3 more
doaj +1 more source