Results 171 to 180 of about 18,178 (201)
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Seminars in pediatric surgery, 1997
Effective diagnosis, staging, and multimodality therapies dramatically decreased the morbidity and mortality of children with Wilms Tumor. Increasing awareness of the disease, biology, genetics, and epidemiology improved assessment of clinical syndromes and led to more risk-based treatment.
G M, Haase, M L, Ritchey
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Effective diagnosis, staging, and multimodality therapies dramatically decreased the morbidity and mortality of children with Wilms Tumor. Increasing awareness of the disease, biology, genetics, and epidemiology improved assessment of clinical syndromes and led to more risk-based treatment.
G M, Haase, M L, Ritchey
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Journal of Cancer Research and Clinical Oncology, 1989
The cases of extrarenal nephroblastoma published in the world literature have been tabulated and reviewed, and are discussed from a historical point of view.
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The cases of extrarenal nephroblastoma published in the world literature have been tabulated and reviewed, and are discussed from a historical point of view.
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Journal of the American Animal Hospital Association, 1997
An eight-month-old, female, mixed-breed dog was presented with bilateral hind-limb paralysis that reportedly developed over a two-to-three week period and was not associated with trauma. Plain radiographs of the spinal column were unremarkable, and a myelogram outlined an intramedullary mass of the spinal cord at the first lumbar (L1) vertebra.
N P, Macri, W, Van Alstine, R A, Coolman
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An eight-month-old, female, mixed-breed dog was presented with bilateral hind-limb paralysis that reportedly developed over a two-to-three week period and was not associated with trauma. Plain radiographs of the spinal column were unremarkable, and a myelogram outlined an intramedullary mass of the spinal cord at the first lumbar (L1) vertebra.
N P, Macri, W, Van Alstine, R A, Coolman
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Current Opinion in Urology, 2001
Wilms' tumor (nephroblastoma) is a subject which continues to challenge clinicians in their attempts to achieve the best survival of their patients, while minimizing morbidity. Overall survival of over 85% of all children can now be achieved using combination therapy with chemotherapy, surgery, and in some cases radiotherapy.
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Wilms' tumor (nephroblastoma) is a subject which continues to challenge clinicians in their attempts to achieve the best survival of their patients, while minimizing morbidity. Overall survival of over 85% of all children can now be achieved using combination therapy with chemotherapy, surgery, and in some cases radiotherapy.
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Journal of Urology, 1984
Nephroblastoma, or Wilms tumor, is the most common renal neoplasm in children and accounts for approximately a fifth of all malignant growths in this age group. However, the incidence of Wilms tumor in adults is much less common, with less than 200 cases having been reported in the literature.
D R, Roth +3 more
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Nephroblastoma, or Wilms tumor, is the most common renal neoplasm in children and accounts for approximately a fifth of all malignant growths in this age group. However, the incidence of Wilms tumor in adults is much less common, with less than 200 cases having been reported in the literature.
D R, Roth +3 more
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Extrarenal Adult Nephroblastoma
Clinical Nuclear Medicine, 2003Ga-67 scintigraphy, abdominal computed tomography (CT), and pelvic magnetic resonance imaging (MRI) were performed in a patient with extrarenal adult nephroblastoma. CT showed a large intra-abdominal cystic tumor displacing the liver and the right kidney. MRI revealed a pelvic tumor with cystic changes.
Naoto, Watanabe +5 more
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European Journal of Pediatrics, 1979
A benign cystic nephroblastoma in a 6-month-old boy is presented. Erroneous interpretation as malignant nephroblastoma led to unnecessarily aggressive therapy. There is no evidence of recurrence or metastatic disease 12 years after the initial resection.
W, Havers, C, Stambolis
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A benign cystic nephroblastoma in a 6-month-old boy is presented. Erroneous interpretation as malignant nephroblastoma led to unnecessarily aggressive therapy. There is no evidence of recurrence or metastatic disease 12 years after the initial resection.
W, Havers, C, Stambolis
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Scottish Medical Journal, 1971
The results of treatment of 45 patients with nephroblastoma in the period 1953–1968 are presented. The overall three year survival rate is 27% while for those given radiotherapy and repeated courses of Actinomycin D following operation the three year survival rate is 40%. The results reported from other centres are discussed.
G F, Milligan, D G, Young
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The results of treatment of 45 patients with nephroblastoma in the period 1953–1968 are presented. The overall three year survival rate is 27% while for those given radiotherapy and repeated courses of Actinomycin D following operation the three year survival rate is 40%. The results reported from other centres are discussed.
G F, Milligan, D G, Young
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Fetal Rhabdomyomatous Nephroblastoma
Journal of Urology, 1983A case of fetal rhabdomyomatous nephroblastoma is reported. The neoplasm distended the renal pelvis, resembling a sarcoma botryoides. The patient died postoperatively of pneumonia and an autopsy showed no residual neoplasm.
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