Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Liora Kornreich"'
Autor:
Karny Shouchane-Blum, Iftach Yassur, Amir Sternfeld, Miriam Regev, Orly Gal-Or, Liora Kornreich, Rita Ehrlich, Miriam Ehrenberg
Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 2, Pp 396-401 (2021)
Lymphatic-venous malformations (LVMs) are development defects that result in abnormal connections between the lymphatic and venous systems. The authors describe a 7-weeks-old female infant who presented with a right orbital LVM extending to the ipsil
Externí odkaz:
https://doaj.org/article/ad6a75d1b367452c805b0bef2ecb3d53
Publikováno v:
Acta Paediatrica.
Autor:
Merav Birk-Bachar, Hadar Cohen, Efrat Sofrin-Drucker, Nesia Kropach-Gilad, Naama Orenstein, Gabriel Lidzbarsky, Liora Kornreich, Rotem Tal, Gil Amarilyo, Yoel Levinsky, Meirav Sokolov, Eyal Raveh, Motti Gerlic, Liora Harel
Cryopyrin-associated periodic syndromes (CAPS) also known as NLRP3-associated auto-inflammatory diseases, are a spectrum of rare auto-inflammatory diseases caused by gain-of-function mutations in the NLRP3 gene, resulting in inflammasome hyper-activa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::002ff43c275b94bffaed968a3afa8a1b
https://doi.org/10.1101/2023.05.05.23289337
https://doi.org/10.1101/2023.05.05.23289337
Autor:
Lotem Goldberg, Zvi Laron, Liora Kornreich, Oded Scheuerman, Hadassa Goldberg-Stern, Dror Kraus
Publikováno v:
Hormone Research in Paediatrics. 95:286-290
Objective: The aim of the study was to describe focal epilepsy in patients with Laron syndrome (LS). Methods: Data were retrieved from medical records of a single-center cohort of 75 patients with LS. Results: We describe for the first time 4 patient
Autor:
Iftach Yassur, Rita Ehrlich, Miriam Regev, Karny Shouchane-Blum, Miriam Ehrenberg, Orly Gal-Or, Liora Kornreich, Amir Sternfeld
Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 2, Pp 396-401 (2021)
Case Reports in Ophthalmology
Case Reports in Ophthalmology
Lymphatic-venous malformations (LVMs) are development defects that result in abnormal connections between the lymphatic and venous systems. The authors describe a 7-weeks-old female infant who presented with a right orbital LVM extending to the ipsil
Publikováno v:
International journal of pediatric otorhinolaryngology. 156
A typical presentation of congenital cholesteatoma (CC) is asymmetric conductive hearing loss (CHL). As CHL is usually associated with middle ear effusion, diagnosis of CC is frequently delayed. This study aimed to describe the clinical characteristi
Publikováno v:
Neuropediatrics. 53(1)
Background We aimed to find the clinical significance of brain abnormalities on magnetic resonance imaging (MRI) in epilepsy and the lateralization of these findings with electroencephalogram (EEG). Methods We retrospectively analyzed the results of
Publikováno v:
Ear, nose,throat journal.
Congenital unilateral choanal atresia (CA) is not considered an emergent condition and should not cause respiratory distress in the newborn. Therefore, surgical repair of unilateral CA is usually delayed. This description of a newborn with congenital
Autor:
Eyal Yosefof, Dan Yaniv, Sharon Tzelnick, Meirav Sokolov, David Ulanovski, Eyal Raveh, Liora Kornreich, Ohad Hilly
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 158:111172
Non-echo-planar diffusion weighted magnetic resonance imaging (Non-EPI DWI MRI) is commonly used for follow-up after cholesteatoma surgery. MRI has a critical role in the evaluation of residual disease, where physical examination will commonly demons
Autor:
David Tal, Liora Kornreich, Dean Ad-El, Leon Gillman, Eyal Kalish, Nesia Kropach, Asaf Olshinka, David A. Staffenberg, Dafna Shilo Yaacobi
Publikováno v:
The Journal of craniofacial surgery. 32(1)
The aim of this report is to describe the combination of Crouzon syndrome and acanthosis nigricans with fibrous dysplasia of the maxilla. The diagnosis of fibrous dysplasia was confirmed clinically and pathologically during Le Fort III osteotomy and