Childhood abdominal cystic lymphangioma

O Konen, V Rathaus, E Dlugy, E Freud, A Kessler… - Pediatric …, 2002 - Springer
Background: Abdominal lymphangioma is a rare benign congenital malformation of the
mesenteric and/or retroperitoneal lymphatics. Clinical presentation is variable and may be …

Differential diagnosis of intracranial cystic lesions at head US: correlation with CT and MR imaging

…, A Daneman, SI Blaser, C Ortiz-Neira, O Konen… - Radiographics, 2006 - pubs.rsna.org
The differential diagnosis of intracranial cystic lesions at head ultrasonography (US) includes
a broad spectrum of conditions: (a) normal variants, (b) developmental cystic lesions, (c) …

Is congenital lobar emphysema a surgical disease?

M Mei-Zahav, O Konen, D Manson… - Journal of pediatric surgery, 2006 - Elsevier
BACKGROUND: The management of congenital lobar emphysema has traditionally been
surgical. Because of increased use of imaging, this lesion is frequently found in asymptomatic …

Long COVID-19 liver manifestation in children

S Cooper, A Tobar, O Konen, N Orenstein… - Journal of pediatric …, 2022 - journals.lww.com
Objectives: Severe acute respiratory syndrome coronavirus 2, the novel coronavirus responsible
for coronavirus disease (COVID-19), has been a major cause of morbidity and mortality …

[PDF][PDF] eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation

…, J Altmüller, P Frommolt, K Hofmann, O Konen… - Molecular cell, 2012 - cell.com
Together with GTP and initiator methionyl-tRNA, translation initiation factor eIF2 forms a
ternary complex that binds the 40S ribosome and then scans an mRNA to select the AUG start …

Neonatal encephalopathy: a prospective comparison of head US and MRI

…, A Daneman, CJ Kellenberger, A Aziz, O Konen… - Pediatric …, 2010 - Springer
Background Head US, the cornerstone neuroimaging modality in neonates, is believed to be
less sensitive than MRI for detecting hypoxic ischemic injury (HII). Most reports comparing …

[PDF][PDF] Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome

…, S Abdelhak, M Pasmanik-Chor, O Konen… - The American Journal of …, 2012 - cell.com
Ubiquitination plays a crucial role in neurodevelopment as exemplified by Angelman syndrome,
which is caused by genetic alterations of the ubiquitin ligase-encoding UBE3A gene. …

[PDF][PDF] Infantile cerebral and cerebellar atrophy is associated with a mutation in the MED17 subunit of the transcription preinitiation mediator complex

…, A Naamati, A Shaag, S Zenvirt, O Konen… - The American Journal of …, 2010 - cell.com
Primary microcephaly of postnatal onset is a feature of many neurological disorders, mostly
associated with mental retardation, seizures, and spasticity, and it typically carries a grave …

Congenital pulmonary venolobar syndrome: spectrum of helical CT findings with emphasis on computerized reformatting

E Konen, L Raviv-Zilka, RA Cohen, M Epelman… - Radiographics, 2003 - pubs.rsna.org
The term congenital pulmonary venolobar syndrome refers to a wide spectrum of pulmonary
developmental anomalies that may appear singly or in combination. The main components …

Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability

…, EMJ Boon, L Basel-Salmon, O Konen… - The Journal of …, 2020 - Am Soc Clin Investig
Epigenetic integrity is critical for many eukaryotic cellular processes. An important question
is how different epigenetic regulators control development and influence disease. Lysine …