Results 201 to 210 of about 29,311 (229)
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International Journal of Radiation Oncology*Biology*Physics, 1980
Abstract Twenty children with bilateral Wilms' tumor presented to the Children's Hospital Medical Center and Children's Cancer Research Foundation, Sidney Farber Cancer Institute, and Joint Center for Radiation Therapy (CHM-CCCRF, SFCI, JCRT) from January 1, 1956 to December 31, 1976. Of these 20, 16 had simultaneous and 4 had metachronous disease on
A W, Malcolm +3 more
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Abstract Twenty children with bilateral Wilms' tumor presented to the Children's Hospital Medical Center and Children's Cancer Research Foundation, Sidney Farber Cancer Institute, and Joint Center for Radiation Therapy (CHM-CCCRF, SFCI, JCRT) from January 1, 1956 to December 31, 1976. Of these 20, 16 had simultaneous and 4 had metachronous disease on
A W, Malcolm +3 more
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2010
Wilms' tumor or nephroblastoma is the most frequent renal tumor in children and is associated with different congenital anomalies and syndromes. A significant number of studies in genetics and molecular biology have improved our understanding of this malignancy discovering as well how different genes play a critical role in the organogenesis process ...
Carlos H, Martínez +2 more
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Wilms' tumor or nephroblastoma is the most frequent renal tumor in children and is associated with different congenital anomalies and syndromes. A significant number of studies in genetics and molecular biology have improved our understanding of this malignancy discovering as well how different genes play a critical role in the organogenesis process ...
Carlos H, Martínez +2 more
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Radiology, 1968
The angiographic patterns of renal carcinoma were extensively studied and described by Boijsen and Folin (1) in 1961. Numerous additional reports have accumulated in the literature in the differential considerations of benign and malignant tumors, but nowhere have we been able to find a report on the angiographic patterns of Wilms's tumor.
J, Farah, J E, Lofstrom
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The angiographic patterns of renal carcinoma were extensively studied and described by Boijsen and Folin (1) in 1961. Numerous additional reports have accumulated in the literature in the differential considerations of benign and malignant tumors, but nowhere have we been able to find a report on the angiographic patterns of Wilms's tumor.
J, Farah, J E, Lofstrom
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Journal of Urology, 1979
A review of the literature reveals that Wilms tumor is rare in adolescence. At the time of diagnosis 78 per cent of children are less than 5 years old. Of 17 cases of Wilms tumor seen at the Ontario Cancer Foundation Clinic in Kingston from 1973 to 1975, 3 children were between 16 and 17 years old.
K, Shah, S, Wasan, S, Lott
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A review of the literature reveals that Wilms tumor is rare in adolescence. At the time of diagnosis 78 per cent of children are less than 5 years old. Of 17 cases of Wilms tumor seen at the Ontario Cancer Foundation Clinic in Kingston from 1973 to 1975, 3 children were between 16 and 17 years old.
K, Shah, S, Wasan, S, Lott
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Archives of Pediatrics & Adolescent Medicine, 1979
Extrarenal Wilms' tumor is a rare entity usually seen as a mass in the retroperitoneal area. It may surround and distort otherwise normal kidneys and ureters. Like many other abdominal masses, its true nature remains uncertain until microscopic examination has been performed after surgery.
R G, McCauley +3 more
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Extrarenal Wilms' tumor is a rare entity usually seen as a mass in the retroperitoneal area. It may surround and distort otherwise normal kidneys and ureters. Like many other abdominal masses, its true nature remains uncertain until microscopic examination has been performed after surgery.
R G, McCauley +3 more
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Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 1993
Multiple 'WT' genes exist. The WT1 gene at chromosomal band 11p13 has been cloned and is known to be important in the etiology of at least some tumors by virtue of the identification of both germline and somatic mutations in WT patients. Genes at 11p15 and 16q are also involved, either as initiating or tumor progression events.
V, Huff, G F, Saunders
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Multiple 'WT' genes exist. The WT1 gene at chromosomal band 11p13 has been cloned and is known to be important in the etiology of at least some tumors by virtue of the identification of both germline and somatic mutations in WT patients. Genes at 11p15 and 16q are also involved, either as initiating or tumor progression events.
V, Huff, G F, Saunders
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Journal of Surgical Oncology, 1988
AbstractTwo well‐documented cases of Wilms' tumor in adult patients are reported. Surgery remains the treatment of choice in stage I cases with favorable cell differentiation. Adjuvant therapy with chemotherapy or radiation may be necessary in patients beyond stage I or when the cell differentiation is more anaplastic.
S Y, Chang, C P, Ma, W H, Lee
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AbstractTwo well‐documented cases of Wilms' tumor in adult patients are reported. Surgery remains the treatment of choice in stage I cases with favorable cell differentiation. Adjuvant therapy with chemotherapy or radiation may be necessary in patients beyond stage I or when the cell differentiation is more anaplastic.
S Y, Chang, C P, Ma, W H, Lee
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Journal of Pediatric Surgery, 2003
The earliest specialists in the field of pediatric surgical oncology were the surgeons of 19th century Europe, particularly Billroth, Kocher, and Wilms. However, the first successful nephrectomy for a Wilms' tumor in a child was performed by a less famous name, Thomas Richard Jessop (1837-1903) at the Leeds General Infirmary on June 7, 1877.
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The earliest specialists in the field of pediatric surgical oncology were the surgeons of 19th century Europe, particularly Billroth, Kocher, and Wilms. However, the first successful nephrectomy for a Wilms' tumor in a child was performed by a less famous name, Thomas Richard Jessop (1837-1903) at the Leeds General Infirmary on June 7, 1877.
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Human Genetics, 1981
The analyses of published data for Wilms' tumor show the following results: 1) The mode of inheritance of familial cases, which constitute less than 1% of all Wilms' tumors, is autosomal dominant with variable penetrance and expressivity. The familial pattern reveals no evidence that this tumor is associated with a vertically transmitting tumor ...
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The analyses of published data for Wilms' tumor show the following results: 1) The mode of inheritance of familial cases, which constitute less than 1% of all Wilms' tumors, is autosomal dominant with variable penetrance and expressivity. The familial pattern reveals no evidence that this tumor is associated with a vertically transmitting tumor ...
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