يعرض 1 - 10 نتائج من 10 نتيجة بحث عن '"S. R. Talypov"', وقت الاستعلام: 0.37s تنقيح النتائج
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    Academic Journal

    المساهمون: The study was performed without external funding, Исследование проведено без спонсорской поддержки

    المصدر: Russian Journal of Pediatric Hematology and Oncology; Том 9, № 4 (2022); 96-101 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 9, № 4 (2022); 96-101 ; 2413-5496 ; 2311-1267

    وصف الملف: application/pdf

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    Academic Journal

    المصدر: Russian Journal of Pediatric Hematology and Oncology; Том 4, № 3 (2017); 97-101 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 4, № 3 (2017); 97-101 ; 2413-5496 ; 2311-1267 ; 10.17650/2311-1267-2017-4-3

    وصف الملف: application/pdf

    Relation: https://journal.nodgo.org/jour/article/view/324/323; Messinger Y.H., Stewart D.R., Priest J.R. et al. Pleuropulmonary blastoma: a report on 350 central pathology-confirmed pleuropulmonary blastoma cases by the International Pleuropulmonary Blastoma Registry. Cancer 2015;121(2):276–85. doi:10.1002/ cncr.29032.; Dehner L.P., Watterson J., Priest J.R. Pleuropulmonary blastoma. A unique intrathoracic-pulmonary neoplasm of childhood. Perspectives in Pediatric Pathology 1995;18:214–26.; Priest J.R., Watterson J., Strong L. et al. Pleuropulmonary blastoma: a marker for familial disease. J Pediatr 1996;128(2):220–4. PMID: 8636815.; Calabria R., Srikanth M.S., Chamberlin K., Bloch J., Atkinson J.B. Management of pulmonary blastoma in children. Am Surg 1993;59(3):192–6. PMID: 8476159.; Wright J.R. Pleuropulmonary blastoma: A case report documenting transition from type I (cystic) to type III (solid). Cancer 2000;88(12):2853–8. PMID: 10870072.; Priest J.R., Hill D.A., Williams G.M. et al. Type I pleuropulmonary blastoma: a report from the International Pleuropulmonary Blastoma Registry. J Clin Oncol 2006;24(27):4492–8. doi:10.1200/ JCO.2005.05.3595.; Priest J.R., Williams G.M., Hill D.A., Dehner L.P., Jaffé A. Pulmonary cysts in early childhood and the risk of malignancy. Pediatr Pulmonol 2009;44(1):14–30. doi:10.1002/ppul.20917.; Hill D.A., Ivanovich J., Priest J.R. et al. DICER1 mutations in familial pleuropulmonary blastoma. Science 2009;325(5943):965. doi:10.1126/science.1174334.; Feinberg A., Hall N.J., Williams G.M. et al. Can congenital pulmonary airway malformation be distinguished from Type I pleuropulmonary blastoma based on clinical and radiological features? J Pediatr Surg 2016;51(1):33–7. doi:10.1016/j.jpedsurg.2015.10.019.; https://journal.nodgo.org/jour/article/view/324

  6. 6
    Academic Journal

    المصدر: Russian Journal of Pediatric Hematology and Oncology; Том 4, № 1 (2017); 83-88 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 4, № 1 (2017); 83-88 ; 2413-5496 ; 2311-1267 ; 10.17650/2311-1267-2017-4-1

    وصف الملف: application/pdf

    Relation: https://journal.nodgo.org/jour/article/view/287/287; Cheung N.K., Dyer M.A. Neuroblastoma: developmental biology, cancer genomics and immunotherapy. Nat Rev Cancer 2013;13(6):397–411.; Berthold F., Simon T. Clinical presentation. In: Neuroblastoma. Cheung N.-K., Cohn S., eds. Springer-Verlag, Berlin, Heidelberg, 2005. Pp. 63–86.; Brodeur G.M., Pritchard J., Berthold F. et al. Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment. J Clin Oncol 1993;11(8):1466–77.; Nour-Eldin N.E., Abdelmonem O., Tawfik A.M. et al. Pediatric primary and metastatic neuroblastoma: MRI findings: pictorial review. Magn Reson Imaging 2012;30(7):893–906.; Качанов Д.Ю., Шаманская Т.В., Муфтахова Г.М., Варфоломеева С.Р. Нейробластома 4S стадии. Вопросы гематологии/онкологии и иммунопатологии в педиатрии 2014;13(2):9–19. [Kachanov D.Yu., Shamanskaya T.V., Muftakhova G.M., Varfolomeeva S.R. Stage 4S neuroblastoma. Voprosy gematologii/onkologii i immunopatologii v pediatrii = Pediatric Hematology/ Oncology and Immunopathology 2014;13(2):9–19. (In Russ.)].; Pagès P.M., Dufour C., Fasola S. et al. Bilateral adrenal neuroblastoma. Pediatr Blood Cancer 2009;52(2):196–202.; Katzenstein H.M., Bowman L.C., Brodeur G.M. et al. Prognostic significance of age, MYCN oncogene amplification, tumor cell ploidy, and histology in 110 infants with stage D(S) neuroblastoma: the pediatric oncology group experience--a pediatric oncology group study. J Clin Oncol 1998;16(6):2007–17.; Schleiermacher G., Michon J., Ribeiro A., et al. Segmental chromosomal alterations lead to a higher risk of relapse in infants with MYCN-non-amplified localised unresectable/ disseminated neuroblastoma (a SIOPEN collaborative study). Br J Cancer 2011;105(12):1940–8.; Massaron S., Seregni E., Luksch R. et al. Neuron-specific enolase evaluation in patients with neuroblastoma. Tumour Biol 1998;19(4):261–8.; Balassy C., Navarro O.M., Daneman A. Adrenal masses in children. Radiol Clin North Am 2011;49(4):711–27.; Brisse H.J., McCarville M.B., Granata S. et al.; International Neuroblastoma Risk Group Project. Guidelines for imaging and staging of neuroblastic tumors: consensus report from the International Neuroblastoma Risk Group Project. Radiology 2011;261(1):243–57.; Rufini V., Shulkin B. The evolution in the use of MIBG in more than 25 years of experimental and clinical applications. Q J Nucl Med Mol Imaging 2008;52(4):341–50.; Mueller W.P., Coppenrath E., Pfluger T. Nuclear medicine and multimodality imaging of pediatric neuroblastoma. Pediatr Radiol 2013;43(4):418–27.; Guglielmi M., De Bernardi B., Rizzo A. et al. Resection of primary tumor at diagnosis in stage IV-S neuroblastoma: does it affect the clinical course? J Clin Oncol 1996;14(5):1537–44.; NB2004 protocol. Berthold F (principal investigator). http://www.kinderkrebsinfo.de/dlja_specialistov/protokoly_gpoh/pohkinderkrebsinfotherapiestudien/nb2004/index_rus.html [cited 2016 March 15].; Holsten T., Schuster T., Grabhorn E. et al. Liver transplantation as a potentially lifesaving measure in neuroblastoma stage 4S. Pediatr Hematol Oncol 2017:1–7. [Epub ahead of print].; van Noesel M.M., Hählen K., Hakvoort-Cammel F.G., Egeler R.M. Neuroblastoma 4S: a heterogeneous disease with variable risk factors and treatment strategies. Cancer 1997;80(5):834–43.; https://journal.nodgo.org/jour/article/view/287

  7. 7
    Academic Journal

    المصدر: Russian Journal of Pediatric Hematology and Oncology; Том 3, № 2 (2016); 87-88 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 3, № 2 (2016); 87-88 ; 2413-5496 ; 2311-1267 ; 10.17650/2311-1267-2016-3-2

    وصف الملف: application/pdf

    Relation: https://journal.nodgo.org/jour/article/view/220/216; Collins M.H., Chatten J. Lipoblastoma/ lipoblastomatosis: a clinicopathologic study of 25 tumors. Am J Surg Pathol 1997;21(10):1131–7.; Yada K., Ishibashi H., Mori H., Shimada M. Intrascrotal lipoblastoma: report of a case and the review of literature. Surg Case Rep 2016;2(1):34.; Posey Y., Valdivia E., Persons D.L. et al. Lipoblastoma presenting as a mesenteric mass in an infant. J Pediatr Hematol Oncol 1998;20(6):580–2.; Dilley A.V., Patel D.L., Hicks M.J., Brandt M.L. Lipoblastoma: pathophysiology and surgical management. J Pediatr Surg 2001;36(1):229–31.; Dal Cin P., Sciot R., De Wever I. et al. New discriminative chromosomal marker in adipose tissue tumors. The chromosome 8q11-q13 region in lipoblastoma. Cancer Genet Cytogenet 1994;78(2):232–5.; Robb A., Rogers T., Nicholls G. A tale of 3 testes? A rare presentation of lipoblastoma with a novel karyotype. J Pediatr Surg 2010;45(1):E29–31.; Kok K.Y., Telisinghe P.U. Lipoblastoma: clinical features, treatment, and outcome. World J Surg 2010;34(7):1517–22.; https://journal.nodgo.org/jour/article/view/220

  8. 8
    Academic Journal

    المصدر: Russian Journal of Pediatric Hematology and Oncology; Том 3, № 2 (2016); 79-86 ; Российский журнал детской гематологии и онкологии (РЖДГиО); Том 3, № 2 (2016); 79-86 ; 2413-5496 ; 2311-1267 ; 10.17650/2311-1267-2016-3-2

    وصف الملف: application/pdf

    Relation: https://journal.nodgo.org/jour/article/view/219/215; Simon T., Häberle B., Hero B. et al. Role of surgery in the treatment of patients with stage 4 neuroblastoma age 18 months or older at diagnosis. J Clin Oncol 2013;31(6):752–8.; Buse S., Gilfrich C., Wagener N. et al. Thoracoabdominal approach to large retroperitoneal tumours. BJU Int 2006;98(5):969–72.; Surgue M. Abdominal compartment syndrome. Curr Opin Crit Care 2005;11:333–8.; Hebra A., Powell D.D., Smith C.D. et al. Balloon tracheoplasty in children: results of a 15-year experience. J Pediatr Surg 1991;26:957–61.; Maeda K., Yasuhuku M., Yamamoto T. A new approach to the treatment of congenital tracheal stenosis: balloon tracheoplasty and expandable metallic stenting. J Pediatr Surg 2001;36:1646–9.; Lusk R. Computer-assisted functional endoscopic sinus surgery in children. Otolaryngol Clin North Am 2005;38(3):505–13.; Wise S.K., Del Gaudio J.M. Computer-aided surgery of the paranasal sinuses and skull base. Expert Rev Med Devices 2005;2(4):395–408.; Tschopp K.P., Thomaser E.G. Outcome of functional endonasal sinus surgery with and without CT-navigation. Rhinology 2008;46:116–20.; Liu X.L., Wu C.W., Zhao Y.S. et al. Exclusive real-time monitoring during recurrent laryngeal nerve dissection in conventional monitored thyroidectomy. Kaohsiung J Med Sci 2016;32(3):135–41.; Minahan R.E., Mandir A.S. Neurophysiologic intraoperative monitoring of trigeminal and facial nerves. J Clin Neurophysiol 2011;28(6):551–65.; Ishimaru M., Ono S., Suzuki S. et al. Risk Factors for Free Flap Failure in 2,846 Patients With Head and Neck Cancer: A National Database Study in Japan. J Oral Maxillofac Surg 2016. pii: S0278-2391(16)00024-0. [Epub ahead of print].; Jacob L.M., Dong W., Chang D.W. Outcomes of reconstructive surgery in pediatric oncology patients: Review of 10-year experience. Ann Surg Oncol 2010;17:2563–9.; Rodriguez-Merchan E.C. The haemophilic pseudotumour. Haemophilia 2002;8(1):12–6.; https://journal.nodgo.org/jour/article/view/219

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