Results 81 to 90 of about 1,664 (151)

Nasal glial heterotopia – Clinical manifestation in 2.5 month-old boy

open access: yes, 2019
Nasal glial heterotopia is a rare congenital defect that is formed during embryonic development. This lesion is a part of a larger group of diseases, congenital midline nasal tumors, that occur with a frequency of one per 20,000-40,000 live births ...
Szydłowski, Jarosław   +5 more
core  

Unique presentation of oral glial choristoma in a middle aged lady post teeth extraction with osteomyelitis; A case report

open access: yesIndian Journal of Pathology and Microbiology
Glial choristoma (GC) is a rare developmental malformation commonly occur in nasal cavity and infrequently present at other sites like palate, tongue, pharynx, lips, and submandibular region.
Rakesh K. Gupta   +2 more
doaj   +1 more source

Glial Heterotopia of the Middle Ear: First Case in Indian Literature. [PDF]

open access: yesIndian J Otolaryngol Head Neck Surg, 2023
Ankita S   +5 more
europepmc   +1 more source

ePosters Virtual

open access: yes
European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Periventricular Heterotopia: Shuttling of Proteins through Vesicles and Actin in Cortical Development and Disease

open access: yesScientifica, 2012
During cortical development, proliferating neural progenitors exhibit polarized apical and basolateral membranes that are maintained by tightly controlled and membrane-specific vesicular trafficking pathways.
Volney L. Sheen
doaj   +1 more source

Endoscopic Repair of Nasopharyngeal Glial Heterotopia in a Neonate with Persistent Craniopharyngeal Canal: A Case Report. [PDF]

open access: yesIndian J Otolaryngol Head Neck Surg, 2023
Raman EV   +4 more
europepmc   +1 more source

A Rare Case of Nasal Glial Heterotopia Presenting as Sphenochoanal Polyp*

open access: yes, 2015
Objective: This paper reports a rare case of nasal glial heterotopia presenting as sphenochoanal polyp. So far, literature has revealed only few cases.
Pavol Surda, Jonathan Hobson
core  

Neuronal migration defects in the Dreher (Lmx1a) mutant mouse: role of disorders of the glial limiting membrane [PDF]

open access: yes, 2001
Dreher (dr(J)) is an autosomal recessive mutation in the newly identified LIM homeobox gene, Lmx1a. The homozygous mutant phenotype includes misplaced neurons (heterotopia) in the cerebral cortex, cerebellum and hippocampus, which mimic the mild end of ...
Harding, B, Costa, C, Copp, A
core  

A report on gray matter heterotopias and neuropsychiatric manifestation: A bleary phenomenon

open access: yesArchives of Mental Health
Malformations of the cortical system are associated with many neuropsychiatric manifestations. Gray matter heterotopia is a neuronal migration disorder characterized by the presence of normal gray matter neurons and glial cells, which are abnormally ...
Vishnupriya Veeraraghavan
doaj   +1 more source

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