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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1954 1
1956 1
1959 1
1961 1
1962 2
1964 1
1965 4
1966 15
1967 17
1968 29
1969 47
1970 47
1971 52
1972 55
1973 52
1974 52
1975 74
1976 73
1977 64
1978 62
1979 66
1980 66
1981 63
1982 59
1983 49
1984 75
1985 76
1986 71
1987 72
1988 71
1989 99
1990 76
1991 67
1992 87
1993 85
1994 86
1995 87
1996 83
1997 82
1998 92
1999 80
2000 108
2001 95
2002 98
2003 109
2004 98
2005 94
2006 101
2007 108
2008 123
2009 125
2010 133
2011 132
2012 145
2013 143
2014 136
2015 132
2016 126
2017 124
2018 116
2019 76
2020 2
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4,322 results
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Page 1
Rhabdomyosarcoma.
Dasgupta R, et al. Semin Pediatr Surg 2016 - Review. PMID 27955730
A malignant tumor of striated muscle origin, rhabdomyosarcoma (RMS) is a childhood tumor that has benefited from nearly 30 years of multimodality therapy, culminating in a >70% overall 5-year survival. ...
A malignant tumor of striated muscle origin, rhabdomyosarcoma (RMS) is a childhood tumor that has benefited from nearly 30 years of m …
Consensus and controversies regarding the treatment of rhabdomyosarcoma.
Borinstein SC, et al. Pediatr Blood Cancer 2018 - Review. PMID 28905489
Optimal treatment of rhabdomyosarcoma (RMS) requires multidisciplinary approach, incorporating chemotherapy with local control. ...
Optimal treatment of rhabdomyosarcoma (RMS) requires multidisciplinary approach, incorporating chemotherapy with local control. ...
Rhabdomyosarcoma: an overview and nursing considerations.
Kerin Ú, et al. Br J Nurs 2018 - Review. PMID 29561665
This article aims to provide nurses with a clinical overview of rhabdomyosarcoma, a rare type of soft tissue sarcoma. The causes, clinical features, pathophysiology, diagnostic process, prognosis and treatment will be explored. Some of the main nursing considerations for rhabdomyosarcoma patients will be discussed in light of current treatment recommendations....
This article aims to provide nurses with a clinical overview of rhabdomyosarcoma, a rare type of soft tissue sarcoma. The causes, cli …
Worse Outcomes for Head and Neck Rhabdomyosarcoma Secondary to Reduced-Dose Cyclophosphamide.
Casey DL, et al. Int J Radiat Oncol Biol Phys 2019. PMID 30508617 Free PMC article.
PURPOSE: Recent trends, including the use of proton therapy and administration of reduced doses of cyclophosphamide, have been adapted in head and neck (HN) rhabdomyosarcoma (RMS) to reduce late morbidity. ...Longer follow-up is needed to further assess disease outcomes with proton therapy....
PURPOSE: Recent trends, including the use of proton therapy and administration of reduced doses of cyclophosphamide, have been adapte …
Treatment Approach and Outcomes in Infants With Localized Rhabdomyosarcoma: A Report From the Soft Tissue Sarcoma Committee of the Children's Oncology Group.
Bradley JA, et al. Int J Radiat Oncol Biol Phys 2019. PMID 30138647 Free PMC article.
PURPOSE: For infants with localized rhabdomyosarcoma who were enrolled on Children's Oncology Group ARST0331 and ARST0531, local therapy guidelines were provided, but adherence was not mandated because of toxicity concerns. ...Forty-three percent of patients received individualized local therapy (outside protocol guidelines), typically omission or delay of radiation therapy. ...
PURPOSE: For infants with localized rhabdomyosarcoma who were enrolled on Children's Oncology Group ARST0331 and ARST0531, local t
Testicular transposition in children undergoing brachytherapy for bladder and/or prostate rhabdomyosarcoma.
de Lambert G, et al. J Pediatr Surg 2018. PMID 29753523
We describe a new technique of testicular transposition (TT) in patients treated with pulse-dose-rate (PDR) brachytherapy as part of the multimodal conservative treatment of bladder neck and/or prostate rhabdomyosarcoma (BP RMS). ...
We describe a new technique of testicular transposition (TT) in patients treated with pulse-dose-rate (PDR) brachytherapy as part of the mul …
[Rhabdomyosarcoma].
Hosoi H, et al. Gan To Kagaku Ryoho 2007. PMID 17301524 Japanese.
Rhabdomyosarcoma (RMS) is the most common type of soft-tissue sarcoma in childhood. In Europe and the United States, survival rates of RMS patients, especially those with local or regional RMS, have dramatically improved from around 25% in 1970 to over 70% in 2001 as a result of the introduction of multimodality therapy and cooperative group trials. ...We have recently established the Japan Rhabdomyosarcoma Study Group (JRSG) and continued several studies in each risk group to improve the outcome and to establish a standard therapy in Japan....
Rhabdomyosarcoma (RMS) is the most common type of soft-tissue sarcoma in childhood. In Europe and the United States, survival rates o
Rhabdomyosarcoma.
Stuart A and Radhakrishnan J. Indian J Pediatr 2004 - Review. PMID 15107514
Rhabdomyosarcoma, the most common soft tissue sarcoma of children, carried a 10-15% survival rate in the late 1960s. Since then, better understanding of biology and pathology of the tumor and the judicious use of chemotherapy and radiation has improved the prognosis drastically. ...In this article the authors review current information regarding pathology, diagnosis and treatment of rhabdomyosarcoma....
Rhabdomyosarcoma, the most common soft tissue sarcoma of children, carried a 10-15% survival rate in the late 1960s. Since then, bett
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