Results 11 to 20 of about 15,468,962 (298)
Editorial: Volume 19 Issue 2, October 2011
Editorial: Volume 19 Issue 2, October ...
Cathy Stone, Annie Andrews
doaj +1 more source
LIPIcs, Volume 143, WABI'19, Complete Volume [PDF]
LIPIcs, Volume 143, WABI'19, Complete ...
Huber, Katharina T., Gusfield, Dan
core +1 more source
LIPIcs, Volume 142, COSIT'19, Complete Volume [PDF]
LIPIcs, Volume 142, COSIT'19, Complete ...
Stewart, Kathleen +4 more
core +1 more source
LIPIcs, Volume 19, TYPES'11, Complete Volume
LIPIcs, Volume 19, TYPES'11, Complete ...
Danielsson, Nils Anders +1 more
core +1 more source
LIPIcs, Volume 132, ICALP'19, Complete Volume [PDF]
LIPIcs, Volume 132, ICALP'19, Complete ...
Leonardi, Stefano +3 more
core +1 more source
Ewing Sarcoma in Infants and Children Under 2 Years of Age: A French Retrospective Study
ABSTRACT Ewing sarcoma, the second most common primary bone cancer in children, requires intensive treatment that may lead to significant long‐term sequelae, particularly in infants. We retrospectively analyzed data from 1621 French patients treated between 1988 and 2015 within the EW88/93/97 or EE99 trials, focusing on 17 infants diagnosed before 24 ...
Elodie Verdier +18 more
wiley +1 more source
OASIcs, Volume 19, VLUDS'10, Complete Volume
OASIcs, Volume 19, VLUDS'10, Complete ...
Middel, Ariane +2 more
core +1 more source
Global Efforts to Reduce Paediatric Cancer Care Disparities in Radiotherapy: A Decade Change
ABSTRACT Background We present an update on the status, needs and challenges faced by paediatric imaging and radiotherapy (RT) programmes globally after a previous survey conducted by the International Atomic Energy Agency (IAEA) 10 years prior. Methods We developed and distributed a 121‐question survey to radiation oncologists, medical physicists and ...
Raymond B. Mailhot Vega +10 more
wiley +1 more source
ABSTRACT Background Shwachman–Diamond syndrome (SDS) is a rare autosomal recessive ribosomopathy characterized by bone marrow failure and multisystem involvement, with emerging evidence of associated neurocognitive impairment. Methods We conducted a retrospective study of 240 individuals with biallelic Shwachman–Bodian–Diamond syndrome (SBDS) mutations
Jane Koo +11 more
wiley +1 more source
ABSTRACT Purpose Next‐generation sequencing (NGS) has emerged as a promising approach to improve diagnostic accuracy, but its feasibility in low‐ and middle‐income countries remains unknown. This study characterized the diagnostic landscape and assessed organizational readiness for NGS implementation at two childhood cancer treatment centers in Accra ...
Melissa Carvalho +6 more
wiley +1 more source

