Atypical teratoid/rhabdoid tumors—current concepts, advances in biology, and potential future therapies
MC Frühwald, JA Biegel, F Bourdeaut… - Neuro …, 2016 - academic.oup.com
Atypical teratoid/rhabdoid tumor (AT/RT) is the most common malignant CNS tumor of
children below 6 months of age. The majority of AT/RTs demonstrate genomic alterations in …
children below 6 months of age. The majority of AT/RTs demonstrate genomic alterations in …
Atypical teratoid/rhabdoid tumors: challenges and search for solutions
A Biswas, L Kashyap, A Kakkar, C Sarkar… - Cancer management …, 2016 - Taylor & Francis
Atypical teratoid/rhabdoid tumor (AT/RT) is a highly malignant embryonal central nervous
system tumor commonly affecting children< 3 years of age. It roughly constitutes 1%–2% of …
system tumor commonly affecting children< 3 years of age. It roughly constitutes 1%–2% of …
Inhibition of DNA damage repair by the CDK4/6 inhibitor palbociclib delays irradiated intracranial atypical teratoid rhabdoid tumor and glioblastoma xenograft …
R Hashizume, A Zhang, S Mueller, MD Prados… - Neuro …, 2016 - academic.oup.com
Background Radiation therapy is the most commonly used postsurgical treatment for primary
malignant brain tumors. Consequently, investigating the efficacy of chemotherapeutics …
malignant brain tumors. Consequently, investigating the efficacy of chemotherapeutics …
Outcomes and acute toxicities of proton therapy for pediatric atypical teratoid/rhabdoid tumor of the central nervous system
SL McGovern, MF Okcu, MF Munsell… - International Journal of …, 2014 - Elsevier
Purpose Atypical teratoid/rhabdoid tumor (AT/RT) of the central nervous system is a rare
cancer primarily affecting children younger than 5 years old. Because patients are young …
cancer primarily affecting children younger than 5 years old. Because patients are young …
Multimodal therapy in children and adolescents with newly diagnosed atypical teratoid rhabdoid tumor: individual pooled data analysis and review of the literature
D Schrey, F Carceller Lechón, G Malietzis… - Journal of neuro …, 2016 - Springer
Atypical teratoid rhabdoid tumour (ATRT) is a malignant tumour of the central nervous
system with a dismal prognosis. There is no consensus on optimal treatment and different …
system with a dismal prognosis. There is no consensus on optimal treatment and different …
Proton therapy for pediatric malignancies: Fact, figures and costs. A joint consensus statement from the pediatric subcommittee of PTCOG, PROS and EPTN
Radiotherapy plays an important role in the management of childhood cancer, with the
primary aim of achieving the highest likelihood of cure with the lowest risk of radiation …
primary aim of achieving the highest likelihood of cure with the lowest risk of radiation …
Proton therapy for paediatric CNS tumours—improving treatment-related outcomes
V Gondi, TI Yock, MP Mehta - Nature Reviews Neurology, 2016 - nature.com
Radiotherapy is an integral and highly effective aspect of the management of many
paediatric CNS tumours, including embryonal tumours, astrocytic tumours and ependymal …
paediatric CNS tumours, including embryonal tumours, astrocytic tumours and ependymal …
Atypical teratoid/rhabdoid tumor in adults: a systematic review of the literature with meta-analysis and additional reports of 4 cases
G Broggi, F Gianno, DT Shemy, M Massimino… - Journal of neuro …, 2022 - Springer
Introduction Atypical teratoid/rhabdoid tumor (AT/RT) is a highly aggressive embryonal CNS
neoplasm, characterized by inactivation of SMARCB1 (INI1) or rarely of SMARCA4 (BRG1) …
neoplasm, characterized by inactivation of SMARCB1 (INI1) or rarely of SMARCA4 (BRG1) …
Paediatric brain tumours: a review of radiotherapy, state of the art and challenges for the future regarding protontherapy and carbontherapy
Background and purpose Brain tumours are the most frequent solid tumours in children and
the most frequent radiotherapy indications in paediatrics, with frequent late effects: cognitive …
the most frequent radiotherapy indications in paediatrics, with frequent late effects: cognitive …
[HTML][HTML] Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22
SA Koza, AC Tabet, MC Bonaglia, S Andres… - European journal of …, 2023 - Elsevier
This paper focuses on genetic counselling in Phelan-McDermid syndrome (PMS), a rare
neurodevelopmental disorder caused by a deletion 22q13. 3 or a pathogenic variant in …
neurodevelopmental disorder caused by a deletion 22q13. 3 or a pathogenic variant in …