Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1985 1
1991 1
1995 1
1996 1
1998 1
1999 1
2001 1
2005 1
2007 1
2012 1
2013 1
2020 1
2022 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

12 results

Results by year

Filters applied: . Clear all
Page 1
Cancer in infants: a review of 82 cases.
Yang CP, Hung IJ, Jaing TH, Shih LY, Chang WH. Yang CP, et al. Pediatr Hematol Oncol. 2005 Sep;22(6):463-81. doi: 10.1080/08880010591002233. Pediatr Hematol Oncol. 2005. PMID: 16169813 Review.
Acute leukemia was diagnosed in 21 infants (25.6%; acute myeloid leukemia in 12, and acute lymphoblastic leukemia in 9), retinoblastoma in 14 (17.1%), neuroblastoma in 12 (14.6%), brain tumor in 9 (11.0%), germ cell tumor in 8 (9.8%), renal cancer in 8 (Wilms tumor
Acute leukemia was diagnosed in 21 infants (25.6%; acute myeloid leukemia in 12, and acute lymphoblastic leukemia in 9), retinoblastoma in 1 …
Hepatic metastasectomy in children.
Su WT, Rutigliano DN, Gholizadeh M, Jarnagin WR, Blumgart LH, La Quaglia MP. Su WT, et al. Cancer. 2007 May 15;109(10):2089-92. doi: 10.1002/cncr.22650. Cancer. 2007. PMID: 17410597 Free article.
RESULTS: Fifteen patients were identified during this period and primary malignancies included neuroblastoma (7), Wilms tumor (3), osteogenic sarcoma (2), malignant gastric epithelial tumor (1), and desmoplastic small round cell tumor (2). ...
RESULTS: Fifteen patients were identified during this period and primary malignancies included neuroblastoma (7), Wilms tumor
Outcome and cost analysis of operative versus nonoperative management of neonatal multicystic dysplastic kidneys.
Pérez LM, Naidu SI, Joseph DB. Pérez LM, et al. J Urol. 1998 Sep;160(3 Pt 2):1207-11; discussion 1216. doi: 10.1097/00005392-199809020-00070. J Urol. 1998. PMID: 9719312 Review.
The most important reason to perform screening renal ultrasound in this condition is to detect earlier stage Wilms tumor (3 to 10-fold the general pediatric population risk of 1/10,000 cases). ...
The most important reason to perform screening renal ultrasound in this condition is to detect earlier stage Wilms tumor (3
Screening for Wilms' tumor in children with high-risk congenital syndromes: considerations for an intervention trial.
DeBaun MR, Brown M, Kessler L. DeBaun MR, et al. Med Pediatr Oncol. 1996 Nov;27(5):415-21. doi: 10.1002/(SICI)1096-911X(199611)27:5<415::AID-MPO5>3.0.CO;2-P. Med Pediatr Oncol. 1996. PMID: 8827068 Review.
This select population of children 1) are relatively easily identified; 2) have a high incidence of Wilms' tumor; 3) if identified before development of Wilms' tumor, may have a decrement in morbidity/mortality; and 4) are amenable to a simple and acceptable …
This select population of children 1) are relatively easily identified; 2) have a high incidence of Wilms' tumor; 3) if …
Body region-specific 3D age-scaling functions for scaling whole-body computed tomography anatomy for pediatric late effects studies.
Gupta AC, Owens CA, Shrestha S, Lee C, Smith SA, Weathers RE, Netherton T, Balter PA, Kry SF, Followill DS, Griffin KT, Long JP, Armstrong GT, Howell RM. Gupta AC, et al. Biomed Phys Eng Express. 2022 Feb 1;8(2):10.1088/2057-1976/ac3f4e. doi: 10.1088/2057-1976/ac3f4e. Biomed Phys Eng Express. 2022. PMID: 34874300 Free PMC article.
For the feasibility study, eight male and female reference size UF/NCI phantoms (5, 10, 15, and 35 years) were downscaled to fourteen different ages which included next nearest available lower discrete ages (1, 5, 10 and 15 years) and the median ages at the time of RT for Wilm
For the feasibility study, eight male and female reference size UF/NCI phantoms (5, 10, 15, and 35 years) were downscaled to fourteen differ …
Imaging Characteristics of Nephrogenic Rests Versus Small Wilms Tumors: A Report From the Children's Oncology Group Study AREN03B2.
Sandberg JK, Chi YY, Smith EA, Servaes S, Hoffer FA, Mullen EA, Perlman EJ, Tornwall B, Ehrlich PF, Geller JI, Grundy PE, Fernandez CV, Dome JS, Khanna G. Sandberg JK, et al. AJR Am J Roentgenol. 2020 May;214(5):987-994. doi: 10.2214/AJR.19.22301. Epub 2020 Mar 11. AJR Am J Roentgenol. 2020. PMID: 32160052 Free PMC article.
Perilobar rests (17/20) were more likely to be homogeneous than intralobar rests (3/11) or Wilms tumor (3/26) (p < 0.001). ROC analysis showed that the optimal size cutoff for distinguishing between nephrogenic rests and Wilms tumors was 1.75 cm. ...

Perilobar rests (17/20) were more likely to be homogeneous than intralobar rests (3/11) or Wilms tumor (3/26) (p < 0

Birth defects in three common pediatric malignancies; Wilms' tumor, neuroblastoma and Ewing's sarcoma.
Nakissa N, Constine LS, Rubin P, Strohl R. Nakissa N, et al. Oncology. 1985;42(6):358-63. doi: 10.1159/000226064. Oncology. 1985. PMID: 2999670
All patients were evaluated for the presence of congenital abnormalities. Ten of 34 (29%) patients with Wilms' tumor, 3 of 32 (9%) patients with neuroblastoma, and 0 of 18 patients with Ewing's sarcoma were so effected. ...
All patients were evaluated for the presence of congenital abnormalities. Ten of 34 (29%) patients with Wilms' tumor, 3
Melanoma as a subsequent neoplasm in adult survivors of childhood cancer: a report from the childhood cancer survivor study.
Pappo AS, Armstrong GT, Liu W, Srivastava DK, McDonald A, Leisenring WM, Hammond S, Stovall M, Neglia JP, Robison LL. Pappo AS, et al. Pediatr Blood Cancer. 2013 Mar;60(3):461-6. doi: 10.1002/pbc.24266. Epub 2012 Aug 8. Pediatr Blood Cancer. 2013. PMID: 22887858 Free PMC article.
Initial cancer diagnoses included soft tissue and bone sarcoma (n = 15), leukemia (13), lymphoma (14), central nervous system malignancy (5), Wilms tumor (3), and neuroblastoma (1). The cumulative incidence of first subsequent melanoma at 35 years from initia …
Initial cancer diagnoses included soft tissue and bone sarcoma (n = 15), leukemia (13), lymphoma (14), central nervous system malignancy (5) …
Pediatric core needle biopsy: strengths and limitations in evaluation of masses.
Willman JH, White K, Coffin CM. Willman JH, et al. Pediatr Dev Pathol. 2001 Jan-Feb;4(1):46-52. doi: 10.1007/s100240010122. Pediatr Dev Pathol. 2001. PMID: 11200490
Tumor diagnoses were as follows: primitive neuroectodermal tumor (PNET)/Ewing sarcoma (12), malignant lymphoma/Hodgkin's disease (8), rhabdomyosarcoma (4), germ cell tumor (3), Wilms' tumor (3), neuroblastoma (1), sarcoma, not otherwise specified (4), and oth …
Tumor diagnoses were as follows: primitive neuroectodermal tumor (PNET)/Ewing sarcoma (12), malignant lymphoma/Hodgkin's disease (8), rhabdo …
Recovery of natural killer cells after chemotherapy for childhood acute lymphoblastic leukemia and solid tumors.
Alanko S, Salmi TT, Pelliniemi TT. Alanko S, et al. Med Pediatr Oncol. 1995 Jun;24(6):373-8. doi: 10.1002/mpo.2950240607. Med Pediatr Oncol. 1995. PMID: 7715543
In the two standard risk ALL patients tested, the activity was still low at 5 months after therapy. In contrast, the function was normal at 1 month (Wilms' tumor), 3 months (Mb Hodgkin's) and 6 months (Burkitt lymphoma). ...
In the two standard risk ALL patients tested, the activity was still low at 5 months after therapy. In contrast, the function was normal at …
12 results