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1987 1
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2008 1
2012 1
2013 1
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2019 1
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Page 1
Phenotype evolution and health issues of adults with Beckwith-Wiedemann syndrome.
Gazzin A, Carli D, Sirchia F, Molinatto C, Cardaropoli S, Palumbo G, Zampino G, Ferrero GB, Mussa A. Gazzin A, et al. Am J Med Genet A. 2019 Sep;179(9):1691-1702. doi: 10.1002/ajmg.a.61301. Epub 2019 Jul 24. Am J Med Genet A. 2019. PMID: 31339634
Final tall stature was present in 44%. Four patients developed Wilms' Tumor (2, 3, 5, and 10 years, respectively); one hepatoblastoma (22 years); one acute lymphoblastic leukemia (21 years); one adrenal adenoma and testicular Sertoli cell tumor (22 and 24 yea …
Final tall stature was present in 44%. Four patients developed Wilms' Tumor (2, 3, 5, and 10 years, respectively); one …
Long-term physiologic and oncologic outcomes of inferior vena cava thrombosis in pediatric malignant abdominal tumors.
Loh A, Bishop M, Krasin M, Davidoff AM, Langham MR Jr. Loh A, et al. J Pediatr Surg. 2015 Apr;50(4):550-5. doi: 10.1016/j.jpedsurg.2014.11.044. Epub 2014 Dec 2. J Pediatr Surg. 2015. PMID: 25840061
RESULTS: We identified 15 patients (median age, 4.7 years): 12 with Wilms tumor, 2 with hepatoblastoma, and 1 with adrenocortical carcinoma. ...Evidence on which to base strong treatment recommendations is lacking. Few long-term physiologic complications were …
RESULTS: We identified 15 patients (median age, 4.7 years): 12 with Wilms tumor, 2 with hepatoblastoma, and 1 with adre …
Immunohistochemical analysis of gamma catenin in Wilms' tumors.
Basta-Jovanovic G, Gvozdenovic E, Dimitrijevic I, Brasanac D, Jovanovic M, Kalezic N, Baralic I, Radojevic-Skodric S, Arsic D. Basta-Jovanovic G, et al. Fetal Pediatr Pathol. 2008;27(2):63-70. doi: 10.1080/15513810802028704. Fetal Pediatr Pathol. 2008. PMID: 18568994
The aim of our study was to investigate the expression of gamma-catenin in normal kidney and in Wilms' tumor by immunohistochemistry and to correlate the results with tumor stage, histological type, and prognostic group. We investigated 28 cases of Wilms' tumor, …
The aim of our study was to investigate the expression of gamma-catenin in normal kidney and in Wilms' tumor by immunohistochemistry and to …
Second malignancies after autologous hematopoietic cell transplantation in children.
Danner-Koptik KE, Majhail NS, Brazauskas R, Wang Z, Buchbinder D, Cahn JY, Dilley KJ, Frangoul HA, Gross TG, Hale GA, Hayashi RJ, Hijiya N, Kamble RT, Lazarus HM, Marks DI, Reddy V, Savani BN, Warwick AB, Wingard JR, Wood WA, Sorror ML, Jacobsohn DA. Danner-Koptik KE, et al. Bone Marrow Transplant. 2013 Mar;48(3):363-8. doi: 10.1038/bmt.2012.166. Epub 2012 Sep 10. Bone Marrow Transplant. 2013. PMID: 22964594 Free PMC article.
Primary diagnoses included neuroblastoma (39%), lymphoma (26%), sarcoma (18%), central nervous system tumors (14%) and Wilms tumor (2%). Median follow-up was 8 years (range, <1-21 years). ...When compared with age- and gender-matched general population, au …
Primary diagnoses included neuroblastoma (39%), lymphoma (26%), sarcoma (18%), central nervous system tumors (14%) and Wilms tumor
WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin.
Palmer RE, Kotsianti A, Cadman B, Boyd T, Gerald W, Haber DA. Palmer RE, et al. Curr Biol. 2001 Nov 13;11(22):1805-9. doi: 10.1016/s0960-9822(01)00560-7. Curr Biol. 2001. PMID: 11719225 Free article.
In humans with Denys-Drash Syndrome, a heterozygous germline mutation in WT1 is associated with specific defects in glomeruli and an increased risk for developing Wilms Tumor [2,3]. WT1 target genes implicated in cell cycle regulation and cellular proliferati …
In humans with Denys-Drash Syndrome, a heterozygous germline mutation in WT1 is associated with specific defects in glomeruli and an increas …
Mediastinal mass following chemotherapeutic treatment of Hodgkin's disease: recurrent tumor or thymic hyperplasia?
Ford EG, Lockhart SK, Sullivan MP, Andrassy RJ. Ford EG, et al. J Pediatr Surg. 1987 Dec;22(12):1155-9. doi: 10.1016/s0022-3468(87)80727-3. J Pediatr Surg. 1987. PMID: 3440903
Our experience from 1979 to 1986 includes 14 children aged 1 to 17 years (mean 7.4 years) who were identified with new or recurrent mediastinal masses during or after chemotherapeutic treatment for malignant disease (lymphoma 9, Wilms tumor 2, leukemia 1, ost …
Our experience from 1979 to 1986 includes 14 children aged 1 to 17 years (mean 7.4 years) who were identified with new or recurrent mediasti …