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Topic: Al Ewing

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	Ewing Family of Tumors Treatment - National Cancer Institute
		Llombart-Bosch A, Carda C, Peydro-Olaya A, et al.: Soft tissue Ewing's sarcoma.
		Raney RB, Asmar L, Newton WA Jr, et al.: Ewing's sarcoma of soft tissues in childhood: a report from the Intergroup Rhabdomyosarcoma Study, 1972 to 1991.
		Wunder JS, Paulian G, Huvos AG, et al.: The histological response to chemotherapy as a predictor of the oncological outcome of operative treatment of Ewing sarcoma.
	www.cancer.gov /cancertopics/pdq/treatment/ewings/healthprofessional (1601 words)

	How to Treat the Ewing's Family of Sarcomas in Adult Patients -- Scurr and Judson 11 (1): 65 -- The Oncologist
		Adults with Ewing’s sarcoma/primitive neuroectodermal tumor: adverse effect of older age and primary extraosseous disease on outcome.
		Ewing’s family of tumors in adults: multivariate analysis of survival and long-term results of multimodality therapy in 182 patients.
		Prognostic significance of histopathologic response to chemotherapy in nonmetastatic Ewing’s sarcoma of the extremities.
	theoncologist.alphamedpress.org /cgi/content/full/11/1/65 (5045 words)

	Bonetumor.org - The Web's Most Comprehensive Bone Tumor Resource
		Ewing's sarcoma is a highly malignant tumor that is a type of peripheral primitive neuroectodermal tumor (PNET).
		Ewing's sarcoma is found in the lower extremity more than the upper extremity, but any long tubular bone may be affected.
		Ewing's sarcoma is most common in the first and second decade but may affect persons from age 2 to 80.
	bonetumor.org /tumors/pages/page141.html (599 words)

	eMedicine - Ewing Sarcoma : Article by Ludwig G Strauss
		Ewing sarcoma, a highly malignant primary bone tumor that is derived from red bone marrow, was first described by James Ewing in 1921.
		Ewing sarcoma occurs predominantly in whites and, to a lesser extent, in fls and Asians.
		Ewing sarcoma and peripheral neuroepithelioma belong to the Ewing family of tumors (EFTs) and are considered neural tumors.
	www.emedicine.com /radio/topic275.htm (4024 words)

	GulfBase - General Facts about the Gulf of Mexico
		Salt domes are prevalent in the region, and the upward migration of salt is theorized to be a cause of the complex bottom profiles (Worzel et al., 1968).
		The Gulf bottom of the region is characterized by sediment-covered folds that parallel the shore.
		Antoine, J.W. and Ewing, J.I. Seismic refraction measurements on the margins of the Gulf of Mexico.
	www.gulfbase.org /facts.php (2399 words)

	Diario
		RPJ Bunn conosce Ewing e Oxemberg, mentre questi stanno preparando un demo a cui collaborano Aurelium Spitty al sax e M. tto al didgeridoo.
		Al trio Bunn/ Ewing/ Oxemberg si aggiungono Jesper Olsen alla voce e Bruce 80 al clarinetto.
		Febbraio/Marzo 2003, il trio Ewing, Oxemberg, Bunn inizia a provare nuovo materiale tra cui una colonna sonora.
	www.criopalmos.it /DIARIO.htm (754 words)

	Ewing’s Family of Tumors
		Such an approach will result in local control of tumor with acceptable morbidity in most patients.[7,8,9] Radiation therapy to the primary tumor as well as to the sites of metastatic disease should be considered but may interfere with delivery of chemotherapy if too much bone marrow is included in the field.
		Bernstein ML, Devidas M, Lafreniere D, et al.: Intensive therapy with growth factor support for patients with Ewing tumor metastatic at diagnosis: Pediatric Oncology Group/Children's Cancer Group Phase II Study 9457--a report from the Children's Oncology Group.
		Burdach S, Meyer-Bahlburg A, Laws HJ, et al.: High-dose therapy for patients with primary multifocal and early relapsed Ewing's tumors: results of two consecutive regimens assessing the role of total-body irradiation.
	www.webmd.com /cancer/tc/ewings-family-of-tumors-treatment-health-professional-information-nci-pdq-metastatic-tumors-of-the (1005 words)

	Ewing's Sarcoma of the Axial System in Patients Older Than 15 Years: Dismal Prognosis Despite Intensive Multiagent ...
		Ewing sarcoma of the rib: results of an intergroup study with analysis of outcome by timing of resection.
		Ewing's sarcoma: a retrospective study of histological and immunohistochemical factors and their relation to prognosis.
		Ewing's sarcoma of the pelvis: long-term survival and functional outcome.
	jjco.oxfordjournals.org /cgi/content/full/34/11/667 (2908 words)

	Bone Cancer Resources and Information \| OncoLink Ewing's Sarcoma (Site not responding. Last check: 2007-11-07)
		Wunder JS, Paulian G, Huvos AG, et al.: The histological response to chemotherapy as a predictor of the oncological outcome of operative treatment of Ewing sarcoma.
		Ewing's tumors of bone and soft tissues belong to the group of neoplasms commonly referred to as small round blue cell tumors of childhood.
		Shamberger RC, LaQuaglia MP, Gebhardt MC, et al.: Ewing sarcoma/primitive neuroectodermal tumor of the chest wall: impact of initial versus delayed resection on tumor margins, survival, and use of radiation therapy.
	www.oncolink.com /types/article.cfm?c=1&s=2&ss=16&id=9160 (5650 words)

	Ewing's sarcoma/primitive neuroectodermal tumor (PNET)
		However, the morphological and biological characteristics of Ewing's tumors developing in soft tissues appear to be indistinguishable from those of tumors developing at bone sites.[2,3] PNETs have been referred to by different terms depending on their location and extent of neural differentiation: peripheral neuroepithelioma, Askin tumor, adult neuroblastoma, peripheral neuroblastoma, and primitive neuroectodermal tumors.
		Ewing's sarcomas/primitive neuroectodermal tumors (PNETs) are malignant tumors histologically characterized by uniform, densely packed, small round cells with round nucleoli-free nuclei and indistinct cytoplasm.
		Intensification of the chemotherapy regimen of alternating courses of vincristine/doxorubicin/cyclophosphamide and ifosfamide/etoposide.
	www.uoc.muni.cz /vyuka-onkologie/guidelines/17sarkom/EWINGSA.htm (3491 words)

	Population-based genetic alterations in Ewing's tumors from Japanese and European Caucasian patients -- Ozaki et al. 13 ...
		Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombination.
		Ewing’s sarcoma: evaluation of chemotherapy in 17 cases.
		EWS–FLI-1 and EWS–ERG chimeric mRNAs in Ewing’s sarcoma and primitive neuroectodermal tumor.
	annonc.oxfordjournals.org /cgi/content/full/13/10/1656 (4161 words)

	Ewing's Sarcoma Family of Tumors: Current Management -- Bernstein et al. 11 (5): 503 -- The Oncologist
		by James Ewing in 1921 [12], is composed of a monotonous population
		of Ewing’s sarcoma in vitro and in vivo [142–148].
		Ewing’s sarcoma family of tumor arising in the adrenal gland--possible diagnostic pitfall in pediatric pathology: histologic, immunohistochemical, ultrastructural, and molecular study.
	theoncologist.alphamedpress.org /cgi/content/full/11/5/503 (6684 words)

	Sarcoma Ewing's Family of Tumors Including Primitive Neuroectodermal Tumor (PNET)
		Llombart-Bosch A, Carda C, Peydro-Olaya A, et al.: Soft tissue Ewing's sarcoma: Characterization in established cultures and xenografts with evidence of a neuroectodermic phenotype.
		Raney RB, Asmar L, Newton WA, et al.: Ewing's sarcoma of soft tissues in childhood: a report from the Intergroup Rhabdomyosarcoma Study.
		Rodriguez-Galindo C, Poquette CA, Marina NM, et al.: Hematologic abnormalities and acute myeloid leukemia in children and adolescents administered intensified chemotherapy for the Ewing sarcoma family of tumors.
	www.medhelp.org /lib/cancernet/107968.htm (4594 words)

	Ewing's sarcoma/primitive neuroectodermal tumor (PNET)
		Picci P, Rougraff BT, Bacci G, et al.: Prognostic significance of histopathologic response to chemotherapy in nonmetastatic Ewing's sarcoma of the extremities.
		The successful treatment of patients with Ewing's sarcoma/PNETs requires the use of multidrug chemotherapy, in addition to radiation therapy or surgical therapy to the primary tumor.[1-4] The standard treatment includes vincristine, doxorubicin, and cyclophosphamide (VAdriaC) alternating with ifosfamide and etoposide and appropriate supportive care for the myelotoxicity caused by this regimen.
		The combination of ifosfamide and etoposide has shown activity in Ewing's sarcoma/PNET, and a large randomized clinical trial demonstrated that outcome was improved when the ifosfamide and etoposide combination was given in alternating courses with vincristine, doxorubicin (or actinomycin-D), and cyclophosphamide.[7] Local control can be achieved by surgery and/or radiation or both.
	cancerweb.ncl.ac.uk /cancernet/100021.html (3327 words)

	Ewing's family of tumors: Treatment - Health Professional Information [NCI PDQ] - Providence Health System
		Cytogenetic studies of the EFTs have identified a consistent alteration of the EWS locus on chromosome 22 band q12 that may involve other chromosomes, including 11 or 21.[7,8] Characteristically, the amino terminus of the EWS gene is juxtaposed with the carboxy terminus of another gene.
		Such an approach will result in local control of tumor with acceptable morbidity in most patients.[6,7,8] Radiation therapy to the primary tumor as well as to the sites of metastatic disease should be considered but may interfere with delivery of chemotherapy if too much bone marrow is included in the field.
		Burdach S, Meyer-Bahlburg A, Laws HJ, et al.: High-dose therapy for patients with primary multifocal and early relapsed Ewing's tumors: results of two consecutive regimens assessing the role of total-body irradiation.
	www.providence.org /healthlibrary/contentViewer.aspx?hwid=ncicdr0000062841&serviceArea=generic (5982 words)

	b5media - Al Ewing
		Al Ewing writes comics and the occasional novel, but is most notable for a criminal incident in June 1986, when he broke into the palace with a sponge and a rusty spanner.
		The Queen, on meeting with the intruder, exclaimed “I know you and you cannot sing” whereupon Ewing murmured that her Majesty “should hear [him] play piano”.
		As a bizarre form of community service he was sentenced to write the retro games blog Re:Retro.
	www.b5media.com /al-ewing (101 words)

	Search. : Monterey County Weekly Newspaper
		The man with the plan is Al Ewing, school bus driver by day and DJ (Artisphere Entertainment) of all trades by night.
		Ewing promises to pay top dollar for weekend venues as an incentive of sorts.
		Granted, some of it may not be all that new, but judging from the overall turnout at the club, DeMaria and Ewing are obviously trying to keep their customers satisfied.
	www.montereycountyweekly.com /articles/4197 (686 words)

	gift Al_Ewing - gift-report.com (Site not responding. Last check: 2007-11-07)
		Al Ewing is a writer for British comic 2000 AD, creator of The Ultimate Future Shock and periodic contributor to the comic's Terror Tales and Future Shorts series, variations on their classic Future Shocks format.
		Al is also responsible for the diary of Ralph Dibny.
		Al's debut novel will be published in 2007 by Abaddon Books.
	www.gift-report.com /Al_Ewing (329 words)

	DNA Microarrays Reveal Relationship of Ewing Family Tumors to Both Endothelial and Fetal Neural Crest-Derived Cells and ...
		Mager AM, Grapin-Botton A, Ladjali K, et al The avian fli gene is specifically expressed during embryogenesis in a subset of neural crest cells giving rise to mesenchyme.
		Moritake H, Sugimoto T, Kuroda H, et al Newly established Askin tumor cell line and overexpression of focal adhesion kinase in Ewing sarcoma family of tumors cell lines.
		White JA, Ramshaw H, Taimi M, et al Identification of the human cytochrome P450, P450RAI-2, which is predominantly expressed in the adult cerebellum and is responsible for all-trans-retinoic acid metabolism.
	cancerres.aacrjournals.org /cgi/content/full/64/22/8213 (4812 words)

	Ewing’s Family of Tumors (Site not responding. Last check: 2007-11-07)
		Cytogenetic studies of the EFTs have identified a consistent alteration of the EWS locus on chromosome 22 band q12 that may involve other chromosomes, including 11 or 21.[7] [8] Characteristically, the amino terminus of the EWS gene is juxtaposed with the carboxy terminus of another gene.
		Such an approach will result in local control of tumor with acceptable morbidity in most patients.[7] [8] [9] Radiation therapy to the primary tumor as well as to the sites of metastatic disease should be considered but may interfere with delivery of chemotherapy if too much bone marrow is included in the field.
		Bernstein ML, Devidas M, Lafreniere D, et al.: Intensive therapy with growth factor support for patients with Ewing tumor metastatic at diagnosis: Pediatric Oncology Group/Children's Cancer Group Phase II Study 9457--a report from the Children's Oncology Group.
	www.cancersource.com /Oncology/NCI/48,CDR0000062841 (5887 words)

	Romantica - Pages
		Cel mai discutat subiect al anilor 80, de la Londra la Johannesbrug, din Philadelphia la Hong Kong, n-a fost razboiul din Irak sau criza ostaticilor din Iran, ci impuscarea lui J.R. Ewing, pe 21 martie 1990.
		Cele trei sunt ingerii pazitori ai lui JR Ewing, cele trei secretare.
		S-a inventat berea JR Ewing, al carei slogan era: "daca intrebi cat costa inseamna ca nu ti-o poti permite".
	www.romantica.ro (818 words)

	LinkedIn: Al Ewing
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	www.linkedin.com /pub/2/491/A80 (61 words)

	Ewing's Family of Tumors Treatment - National Cancer Institute
		Metastases: Although the prognosis is thought to be poor, it has been observed that with intensive therapy, survival in patients with ETB who have only pulmonary metastases is higher than for patients with bone or bone marrow metastases.[9,22]
		Routine histopathology: Traditionally, a major distinction has been made between classical Ewingâs sarcoma, which shows minimal evidence of differentiation, and PNET, which shows evidence of neural differentiation; however, the degree of neural differentiation does not influence outcome.[23,24]
		Response to preoperative therapy: Multiple studies have shown that patients with minimal or no residual tumor after presurgical chemotherapy have a significantly better event-free survival compared with patients with larger amounts of viable tumor.[9,12,14,30,31] Massive tumor necrosis after induction chemotherapy is a very favorable sign.[9,10,30,32]
	cancer.gov /cancertopics/pdq/treatment/ewings/healthprofessional (1697 words)

	Ewing’s Family of Tumors
		LOCALIZED: For Ewing’s tumor of bone, the tumor is defined as localized when, by clinical and imaging techniques, it has not spread beyond the primary site or regional lymph nodes.
		Extraosseous Ewing’s has been grouped using the rhabdomyosarcoma staging system [1] shown below:
		Lymph node and, in particular, central nervous system metastases are less common.[2] According to staging systems in common use, this is stage 4 or group IV.
	www.webmd.com /cancer/tc/ewings-family-of-tumors-treatment-health-professional-information-nci-pdq-stage-information (444 words)

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