Results 121 to 130 of about 35,241 (222)

Prevalence and Patterns of Permanent Tooth Agenesis in Patients With Crouzon or Apert Syndrome: A Systematic Review and Meta‐Analysis

Orthodontics &Craniofacial Research, Volume 29, Issue 1, Page 1-11, February 2026.
ABSTRACT Crouzon and Apert syndromes are rare syndromic craniosynostoses frequently associated with craniofacial and dental anomalies, including tooth agenesis. Although individual studies have reported tooth agenesis prevalence data in specific populations, no attempts have been made to systematically synthesise these data.
M. Cecilia Becerril Santos, Edwin M. Ongkosuwito, Alexandra K. Papadopoulou, Gregory S. Antonarakis   +3 more
wiley   +1 more source

Síndrome de Apert, una aproximación para un diagnóstico clínico. Reporte de caso

Salud Uninorte, 2010
Introducción: El síndrome de Apert, o acrocefalosindactilia tipo I, es un síndrome caracterizado por craneosinostosis, acompañada de sindactilia simétrica en las cuatro extremidades, alteraciones maxilofaciales, cutáneas y retardo mental variable.
Diana Ramírez, Wilmar Saldarriaga, Harry Pachajoa, Carolina Isaza   +3 more
doaj  

FGFR2 Positive [PDF]

, 2020
openaire   +1 more source

FGFR2 Gene [PDF]

, 2020
openaire   +1 more source

LBA12 Efficacy of RLY-4008, a highly selective FGFR2 inhibitor in patients (pts) with an FGFR2-fusion or rearrangement (f/r), FGFR inhibitor (FGFRi)-naïve cholangiocarcinoma (CCA): ReFocus trial

Annals of Oncology, 2022
A. Hollebecque, M. Borad, L. Goyal, A. Schram, J.O. Park, P. Cassier, S. Kamath, D. Meng, E. Dotan, R. Kim, V. Sahai, D. Oh, Chiung-Ying Liao, M. Millward, D. R. Perez, C. Ferté, R. Blakesley, B. Wolf, V. Subbiah, R. Kelley   +19 more
semanticscholar   +1 more source

FGFR2 Gene Translocation [PDF]

, 2020
openaire   +1 more source

Publisher Correction: Truncated FGFR2 is a clinically actionable oncogene in multiple cancers

Nature, 2022
D. Zingg, J. Bhin, Julia Yemelyanenko, S. Kas, F. Rolfs, C. Lutz, Jessica K. Lee, S. Klarenbeek, I. Silverman, S. Annunziato, Chang S. Chan, S. Piersma, Timo Eijkman, Madelon Badoux, E. Gogola, Bjørn Siteur, Justin Sprengers, Bim de Klein, Richard de Goeij-de Haas, G. Riedlinger, Hua Ke, R. Madison, Anne Paulien Drenth, Eline van der Burg, Eva Schut, L. Henneman, M. V. van Miltenburg, Natalie Proost, H. Zhen, E. Wientjens, Roebi de Bruijn, J. D. de Ruiter, U. Boon, Renske de Korte-Grimmerink, Bas van Gerwen, L. Féliz, G. Abou-Alfa, J. S. Ross, M. van de Ven, S. Rottenberg, E. Cuppen, A. V. Chessex, Siraj M. Ali, T. Burn, C. Jiménez, S. Ganesan, L. Wessels, J. Jonkers   +47 more
semanticscholar   +1 more source

FGFR2 NP_000132.3:p.S252W [PDF]

, 2020
openaire   +1 more source

The Prognostic Significance and Co-Expression of Fibroblast Growth Factor Receptor 2 and c-Met in Endometrial Cancer

International Journal of Women's Health
Huiqiao Gao, Qi Lu, Jianxin Zhang Department of Obstetrics and Gynecology, Beijing Chao-Yang Hospital Affiliated to Capital Medical University, Beijing, 100020, People’s Republic of ChinaCorrespondence: Jianxin Zhang, Email Jianxin20241031@126 ...
Gao H, Lu Q, Zhang J
doaj  

Calcified chondroid mesenchymal neoplasms with FN1-receptor tyrosine kinase gene fusions including FGFR2, FGFR1, MERTK, NTRK1, and TEK: a molecular and clinicopathologic analysis

Modern Pathology, 2021
Yajuan J. Liu, Wenjing Wang, Jeffrey Yeh, Yuehua Wu, J. Mantilla, C. Fletcher, R. Ricciotti, E. Chen   +7 more
semanticscholar   +1 more source