Orit A Glenn
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Explore the profile of Orit A Glenn including associated specialties, affiliations and a list of published articles.
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67
Citations
1319
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Recent Articles
1.
Russ J, Agarwal S, Venkatesan C, Scelsa B, Vollmer B, Tarui T, et al.
Brain
. 2025 Mar;
PMID: 40048696
Malformations of cortical development (MCDs) are a heterogeneous family of congenital brain malformations that originate from disturbed development of the cerebral cortex. MCDs can arise from primary genetic disorders that...
2.
Kulesz P, Juranek J, Fletcher J, Houtrow A, Bilaniuk L, Pruthi S, et al.
Neuropsychology
. 2025 Feb;
39(2):162-171.
PMID: 39946636
Objective: Many individuals with spina bifida myelomeningocele perform poorly on memory tasks, with hippocampal damage a possible mechanism. This study analyzed quantitative hippocampal, amygdala, and ventricular volumes to determine if...
3.
Gano D, Glenn O, Rand L, Heraty K, Devine P, Norton M, et al.
Prenat Diagn
. 2024 Dec;
PMID: 39739357
No abstract available.
4.
Shear M, Penon-Portmann M, Shieh J, Glenn O, Thiet M, Chetty S, et al.
Neurol Genet
. 2024 Oct;
10(6):e200171.
PMID: 39444647
Background: Congenital myotonic dystrophy type 1 (DM1) is a rare congenital neuromuscular disorder associated with high morbidity and potential early mortality requiring lifelong symptomatic management. Prenatal presentations of DM1 have...
5.
George E, Vassar R, Yu Y, Norton M, Gano D, Glenn O
AJNR Am J Neuroradiol
. 2024 Oct;
PMID: 39366764
Background And Purpose: Schizencephaly is a rare brain anomaly which is increasingly detected in utero. There are limited data on the etiology and outcomes in fetal schizencephaly to guide workup...
6.
George E, Jaimes C, Xu D, Kasprian G, Glenn O
Magn Reson Imaging Clin N Am
. 2024 Jun;
32(3):443-457.
PMID: 38944433
This article provides the readers with practical guidance on how to perform fetal MR imaging, including technical considerations such as scanner field strength and use of appropriate radiofrequency receive coils,...
7.
Gano D, Pardo A, Glenn O, Sherr E
Semin Fetal Neonatal Med
. 2024 Apr;
29(1):101524.
PMID: 38609800
Fetal neurology encompasses the full spectrum of neonatal and child neurology presentations, with complex additional layers of diagnostic and prognostic challenges unique to the specific prenatal consultation. Diverse genetic and...
8.
Leng K, Cadwell C, Devine W, Tihan T, Qi Z, Singhal N, et al.
Neurol Genet
. 2024 Apr;
10(2):e200142.
PMID: 38586598
Objectives: Mosaic gain of chromosome 1q (chr1q) has been associated with malformation of cortical development (MCD) and epilepsy. Hyaline protoplasmic astrocytopathy (HPA) is a rare neuropathologic finding seen in cases...
9.
George E, Russ J, Validrighi A, Early H, Mamlouk M, Glenn O, et al.
AJNR Am J Neuroradiol
. 2024 Jan;
45(2):229-235.
PMID: 38176731
Background And Purpose: Myelin oligodendrocyte glycoprotein-antibody associated disease (MOGAD) is an increasingly recognized cause of demyelinating disease in children. The purpose of this study is to characterize the CNS imaging...
10.
George E, Vassar R, Mogga A, Li Y, Norton M, Gano D, et al.
Pediatr Neurol
. 2023 Aug;
147:63-67.
PMID: 37562171
Background: COL4A1/A2 variants affecting the alpha 1 and 2 chains of type IV collagen are increasingly recognized as a cause of fetal and neonatal intracranial hemorrhage, porencephaly, and schizencephaly. Fetal...