Results 31 to 40 of about 11,690 (228)
Genealogy+CritiqueIf heterotopia is used in various practical ways, we suggest that it can lead to a better understanding of Foucault's archeology. We will argue that heterotopia can be understood as a transcendental.
Kyrian Benkatbach
doaj +2 more sources
Griot : Revista de Filosofia, 2022 Na pós-colônia, a ingovernabilidade depende daqueles que aparecem onde não deviam aparecer, e falam sem autorização para falar. Depende, a rigor, da existência de heterotopias. A questão da espectralidade é, enquanto questão filosófica, a de nossa relação com esses espaços onde os mortos podem estar em aliança com os vivos.
openaire +3 more sources
EscritaCom: Heterotopias / Writewith: Heterotopias
Revista Polis e Psique, 2016 ResumoEste artigo focaliza uma reflexão sobre a escritaCom a partir do conceito de heterotopia. O conceito de heterotopia permitiria uma zona de aproximação e de criação de um espaço outro, na medida em que se considerar que um exercício de escrita se faz em um espaço.
Bernardes, Anita Guazzelli +1 more
openaire +2 more sources
Recessive ARFGEF2 mutation causes progressive microcephaly, epilepsy, and a distinct MRI pattern
Journal of Biochemical and Clinical Genetics, 2018 Background: Periventricular nodular heterotopia, a common form of neuronal heterotopia, is heterogeneous in etiology. Recessive mutations in ARFGEF2 causing microcephaly and periventricular heterotopia have rarely been reported.
Maram Alojair +5 more
doaj +1 more source
Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier +2 more
wiley +1 more source
Secretopathies emerge as a new class of neurocristopathies
Developmental Dynamics, EarlyView.Abstract Neural crest cells are a transient embryonic population of cells that give rise to a wide range of structures, including craniofacial cartilage and bone, peripheral neurons and glia, as well as components of the cardiac outflow tract, among others.
Amanda Teixeira +3 more
wiley +1 more source
Glial heterotopia of the lip: A rare presentation
Indian Journal of Plastic Surgery, 2016 Glial heterotopia represents collections of normal glial tissue in an abnormal location distant to the central nervous system or spinal canal with no intracranial connectivity.
Mehmet Dadaci +3 more
doaj +1 more source
Localizing value of cutaneous ictal phenomena: A systematic review
Epileptic Disorders, EarlyView.Abstract Objective Clinical observation of autonomic signs during seizures can aid in localizing the epileptogenic zone (EZ). We performed a systematic review and meta‐analysis to evaluate the localizing value of ictal cutaneous phenomena—piloerection, sweating, pallor, and flushing—in focal epilepsy and their relevance to presurgical evaluation ...
R. Rocamora +7 more
wiley +1 more source
Band Heterotopia and Lennox-Gastaut Syndrome: A Case Report
, 2018 Heterotopia, referred to as a limited or common neuronal migration disorder, may manifest clinically with mild mental retardation, epileptic seizures, psychiatric symptoms, or systemic disorders.
Mehmet Fatih GÖL, Füsun Ferda ERDOĞAN
core +1 more source
Interpeduncular heterotopia in Joubert syndrome: a previously undescribed MR finding [PDF]
, 2011 The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most often autosomal-recessive disorder with a characteristic malformation of the midhindbrain.
Pietz, J +13 more
core +1 more source