Results 31 to 40 of about 244,614 (241)

SPOP and OTUD7A Control EWS–FLI1 Protein Stability to Govern Ewing Sarcoma Growth

Advanced Science, 2021
Chromosomal translocation results in development of an Ewing sarcoma breakpoint region 1‐Friend leukemia integration 1 (EWS–FLI1) fusion oncogene in the majority of Ewing sarcoma.
Siyuan Su, Jianfeng Chen, Yao Jiang, Ying Wang, Tamara Vital, Jiaming Zhang, Christian Laggner, Kong T. Nguyen, Zhichuan Zhu, Alex W. Prevatte, Natalie K. Barker, Laura E. Herring, Ian J. Davis, Pengda Liu   +13 more
doaj   +1 more source

Effect of Educational Guidelines on Mothers' Knowledge, Reported Practices, and Anxiety regarding their Children having Ewing Sarcoma [PDF]

Egyptian Journal of Health Care
Background: Ewing tumors, also called Ewing sarcomas, are a class of malignancies that originate in the surrounding soft tissues or bones and have a few characteristics as common.
Heba Boshra Shehata, Amal Abo El-Azm Abd El - Rahman Younis, Ohoud Youssef EL-Sheikh, Mai Nour Eldien Mohamed Mohamed Awad, Lamiaa Moustafa Elbosaty, Mariana Erian Shehata   +5 more
doaj   +1 more source

Gastric Ewing Sarcoma identified on a Meckel's scan

Radiology Case Reports, 2020
Ewing Sarcoma is a malignant small round blue cell tumor most commonly found in bones and soft tissues of the axial skeleton and extremities. The Ewing family of tumors, including peripheral neuroectodermal tumor, represent the second most common ...
Lavi Nissim, MD, Gerald Mandell, MD
doaj   +1 more source

EWSR1 (Ewing sarcoma region 1) [PDF]

, 1998
Review on EWSR1 (Ewing sarcoma region 1), with data on DNA, on the protein encoded, and where the gene is ...
Mugneret, F, F Mugneret
core   +1 more source

A congenital soft tissue ewing sarcoma in a newborn patient [PDF]

, 2017
PubMedID: 29168368Congenital Ewing sarcoma is extremely rare. Here we present a newborn baby born with a mass on the left shoulder. Immunohistochemical staining showed congenital Ewing sarcoma.
Hacer Yapıcıoğlu, Ferda Özlü, Mehmet Satar, Mustafa Akçalı, Banu Kozanoğlu, Eray Akay, Kıvılcım Erdoğan, Gülfiliz Gönlüşen   +7 more
core   +2 more sources

Congenital extraskeletal Ewing′s sarcoma of chest wall - A rare case report

Indian Journal of Pathology and Microbiology, 2011
Congenital extraskeletal Ewing′s sarcoma or peripheral primitive neuroectodermal tumor is an extremely uncommon and invariably fatal tumor. We report a case of extraskeletal congenital Ewing′s sarcoma in a female fetus delivered at 34 weeks of gestation ...
Bhagyalakshmi Atla, B Satya Vara Prasad, K Satya Sri, Geeta Vandana   +3 more
doaj   +1 more source

Ewing's sarcoma of the calcaneum

Indian Journal of Medical and Paediatric Oncology, 2017
Ewing's sarcoma of the calcaneum is rare. Radiological features of this tumor can be misinterpreted as other benign bone tumors due to its rarity. The overall prognosis of Ewing's sarcoma of calcaneum is inferior compared to other sites of this tumor.
Sherif, P Ajmal, Santa, A
openaire   +2 more sources

Metastatic Ewing's sarcoma to the right ventricle [PDF]

, 2011
Ewing's sarcoma is a round cell neoplasm derived from neural crest cells that is part of the primitive neuroectodermal tumor (PNET) family. It is a rare, aggressive malignancy that affects young people, most commonly in the second decade of life.
Milliken, Jeffrey, Kirsh, M., Saremi, Farhood, Abolhoda, Amir, Sender, Leonard, Datrice, Nicole   +5 more
core  

Bone and Soft Tissue: Ewing sarcoma [PDF]

, 2020
Ewing sarcoma is a bone or soft tissue sarcoma most commonly diagnosed in adolescents and young adults.
Bailey, Kelly M, Ranganathan, Sarangarajan   +1 more
core   +1 more source

Bone and Soft Tissue Neoplasms in Infants Versus Older Children: A Report From the Cancer in Young People in Canada Program

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background and Aims Infant bone and soft tissue neoplasms present distinct clinical challenges and lack large‐scale data to inform treatment decisions. This study aims to characterize bone and soft tissue neoplasms in infants in Canada and to compare their outcomes with those of older pediatric patients.
Samuel Sassine, Hallie Coltin, Maria Kondyli, Monia Marzouki, Nicolas Prud'homme, Nida Usmani, Rebecca J. Deyell, Lesleigh Abbott, Tony H. Truong, Sapna Oberoi, Ketan Kulkarni, Josée Brossard, Lynette Bowes, Paul Gibson, Sarah McKillop, Roona Sinha, Lillian Sung, Catherine Vezina, Laura Wheaton, Alexandra P. Zorzi, Marie‐Claude Pelland‐Marcotte, Thai Hoa Tran   +21 more
wiley   +1 more source