Zobrazeno 1 - 10 of 53 pro vyhledávání: '"Juan C. Tardío"'
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Cutaneous leishmaniasis: A pathological study of 360 cases with special emphasis on the contribution of immunohistochemistry and polymerase chain reaction to diagnosis
Autor: Juan C. Tardío, Carmen Chicharro, Rocío S. Cardozo, Pedro P. García‐Montero
Publikováno v: Journal of Cutaneous Pathology. 47:1018-1025
Background Traditional methods for the diagnosis of leishmaniasis yield poor sensitivity, which limits its effectiveness in lesions with a low parasite burden. Methods Retrospective pathologic study of 360 cases of cutaneous leishmaniasis and analysi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf241d030578f7b572877748b69559c6
https://doi.org/10.1111/cup.13785
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Protocolo de estudio y estandarización del informe patológico de los tumores de partes blandas malignos y de comportamiento intermedio de adolescentes y adultos
Autor: Juan José Pozo, Julia Cruz, Juan C. Tardío, Silvia Bagué, David Marcilla, Aurora Astudillo, Isidro Machado
Publikováno v: Revista Española de Patología. 50:100-112
Resumen Los sarcomas de partes blandas son neoplasias poco frecuentes, que incluyen una amplia variedad de tipos histologicos, se presentan en cualquier localizacion y muestran una gran heterogeneidad, con solapamiento, en ocasiones, de la morfologia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1fd9a8961e8f02f81cfa45b97243c038
https://doi.org/10.1016/j.patol.2016.12.003
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Protocolo para el estudio de muestras y estandarización del informe patológico de tumores óseos
Autor: Julia Cruz, Silvia Bagué, David Marcilla, Isidro Machado, Aurora Astudillo, Juan C. Tardío, José Juan Pozo
Publikováno v: Revista Española de Patología. 50:34-44
Primary bone neoplasms represent a rare and heterogeneous group of mesenchymal tumours. The prevalence of benign and malignant tumours varies; the latter (sarcomas) account for less than 0.2% of all malignant tumours. Primary bone neoplasms are usual
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ee3cdf3d0216e9e2e421b70ebfe8e7b
https://doi.org/10.1016/j.patol.2016.08.003
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Clear Cell Atypical Fibroxanthoma: Clinicopathological Study of 6 Cases and Review of the Literature With Special Emphasis on the Differential Diagnosis
Autor: Dolores Arias, José A. Aramburu, Fernando Pinedo, Dolores Suárez-Massa, Radia Khedaoui, Miguel Ángel Martínez-González, Carlos Santonja, Juan C. Tardío
Publikováno v: The American Journal of Dermatopathology. 38:586-592
Atypical fibroxanthoma (AFX) is an uncommon dermal-based neoplasm arising on the sun-damaged skin of elderly people. Clear cell AFX is a rare variant with only 12 cases reported until the present date, all of them as case reports, except for 1 small
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a68ffd97654c392482b8492a3624a54
https://doi.org/10.1097/dad.0000000000000465
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10
Defining Ewing and Ewing-like small round cell tumors (SRCT): The need for molecular techniques in their categorization and differential diagnosis. A study of 200 cases
Autor: Lara Navarro, Piero Picci, Juan C. Tardío, Antonio Llombart-Bosch, S V Petrov, Isidro Machado, Samuel Navarro, Antonio Pellín, Apollon I. Karseladze, Katia Scotlandi, Abbas Agaimy
Publikováno v: Annals of Diagnostic Pathology. 22:25-32
Background Differentiation of Ewing sarcoma family of tumors (ESFT) and Ewing-like tumors remains problematic. Certain ESFT with morphological and immunohistochemical (IHC) profiles lack the EWSR1-ETS transcript. To improve diagnostic accuracy we inv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9712870128aa727657d8309e7d4661a2
https://doi.org/10.1016/j.anndiagpath.2016.03.002
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