Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Yehuda Kollander"'
Autor:
Ran Ankory, Assaf Kadar, Doron Netzer, Haggai Schermann, Yair Gortzak, Shlomo Dadia, Yehuda Kollander, Ortal Segal
Publikováno v:
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Osteoid osteomas are benign bone neoplasms that may cause severe pain and limit function. They are commonly treated by radiofrequency ablation (RFA) through a needle inserted into the nidus of the lesion under CT guidance, which i
Externí odkaz:
https://doaj.org/article/cbedb3ebf5d545b1b20d1798d36daf86
Publikováno v:
Journal of Hip Preservation Surgery
This report presents a case of a 37-year-old female with a history of hip pain. Magnetic resonance arthrography revealed loose bodies within the joint and synovial hypertrophy indicative of synovial chondromatosis (SC). Hip arthroscopy revealed free
Publikováno v:
The Israel Medical Association journal : IMAJ. 21(12)
Autor:
Doron Netzer, Haggai Schermann, Yehuda Kollander, Y Gortzak, Ortal Segal, Ran Ankory, Shlomo Dadia, Assaf Kadar
Publikováno v:
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-6 (2019)
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-6 (2019)
Background Osteoid osteomas are benign bone neoplasms that may cause severe pain and limit function. They are commonly treated by radiofrequency ablation (RFA) through a needle inserted into the nidus of the lesion under CT guidance, which is associa
Publikováno v:
Journal of Hip Preservation Surgery
The most common types of cystic lesions around the hip joint are synovial or ganglion cysts. In rare cases, the cysts can compress adjacent structures and cause symptoms to arise. Obturator neuropathy secondary to a hip ganglion cyst is a rare phenom
Autor:
Duha Bacri, Sergey Postovsky, Myriam Weyl Ben Arush, Eugene Vlodavsky, Yehuda Kollander, Daniela Militianu
Publikováno v:
Journal of Pediatric Hematology/Oncology. 32:e50-e53
We present the first reported case of a child with familial expansile osteolysis syndrome (FEO) who developed osteogenic sarcoma (OS) of the iliac bone. A 17-year-old adolescent presented with pain and a mass on the left pelvis. He was from a family
Autor:
Kathryn S.E. Cheah, Zvi Nevo, Zoharia Evron, Dror Robinson, Haim Werner, Meirav Trebicz-Geffen, Yehuda Kollander, Israel Vlodavsky, Kit Fong Law, Mati Fridkin, Tova Glaser, Neta Ilan, Daniel W. Chan
Publikováno v:
International Journal of Experimental Pathology. 89:321-331
The different clinical entities of osteochondromas, hereditary multiple exostoses (HME) and non-familial solitary exostosis, are known to express localized exostoses in their joint metaphyseal cartilage. In the current study biopsies of osteochondrom
Autor:
Sergey Postovsky, Yehuda Kollander, Merav Barzilai, Boris Futerman, Itzhak Meller, Myriam Weyl Ben Arush
Publikováno v:
Journal of Pediatric Hematology/Oncology. 30:189-195
Despite comprehensive management of pediatric sarcomas, only 60% to 70% of children become long-term survivors. This study was undertaken to evaluate whether regular follow-up improves overall survival of children with recurrent sarcomas. The medical
Autor:
Zoharia Evron, Zvi Nevo, Mati Fridkin, Dror Robinson, Natalia Posternak, Yehuda Kollander, Meirav Trebicz-Geffen, Tova Glaser
Publikováno v:
Experimental and Molecular Pathology. 74:40-48
Hereditary osteochondromas are often caused by mutation in the EXT1 gene. The lesions are typified by formation of a "pseudo" growth plate like lesion growing at 60 degrees to the normal growth direction of the bone. Such lesions can be mimicked surg
Autor:
Meirav Trebicz-Geffen, Dror Robinson, Zoharia Evron, Tova Glaser, Matityahu Fridkin, Yehuda Kollander, Israel Vlodavsky, Neta Ilan, Kit Fong Law, Kathryn S. E. Cheah, Danny Chan, Haim Werner, Zvi Nevo
Publikováno v:
International Journal of Experimental Pathology. 90:191-193