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Autor Gloria Patricia Monsalve Arias
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Médico Auditor en Interventoría, Hospital Pablo Tobón Uribe
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Documentos disponibles escritos por este autor (2)
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Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children / Gloria Patricia Monsalve Arias
Título : Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children Tipo de documento : documento electrónico Autores : Gloria Patricia Monsalve Arias, Fecha de publicación : 2017 Títulos uniformes : Journal of The American Society of Nephrology Idioma : Inglés (eng) Palabras clave : Children immunosuppression nephrotic syndrome outcomes podocytopathies steroid resistance Resumen : We investigated the value of genetic, histopathologic, and early treatment response information in prognosing long-term renal outcome in children with primary steroid-resistant nephrotic syndrome. From the PodoNet Registry, we obtained longitudinal clinical information for 1354 patients (disease onset at >3 months and Mención de responsabilidad : Agnes Trautmann, Sven Schnaidt, Beata S Lipska-Ziętkiewicz, Monica Bodria, Fatih Ozaltin, Francesco Emma, Ali Anarat, Anette Melk, Marta Azocar, Jun Oh, Bassam Saeed, Alaleh Gheisari, Salim Caliskan, Jutta Gellermann, Lina Maria Serna Higuita, Augustina Jankauskiene, Dorota Drozdz, Sevgi Mir, Ayse Balat, Maria Szczepanska, Dusan Paripovic, Alexandra Zurowska, Radovan Bogdanovic, Alev Yilmaz, Bruno Ranchin, Esra Baskin, Ozlem Erdogan, Giuseppe Remuzzi, Agnieszka Firszt-Adamczyk, Elzbieta Kuzma-Mroczkowska, Mieczyslaw Litwin, Luisa Murer, Marcin Tkaczyk, Helena Jardim, Anna Wasilewska, Nikoleta Printza, Kibriya Fidan, Eva Simkova, Halina Borzecka, Hagen Staude, Katharina Hees, Franz Schaefer, PodoNet Consortium Referencia : J Am Soc Nephrol. 2017 Oct;28(10):3055-3065. DOI (Digital Object Identifier) : 10.1681/ASN.2016101121 PMID : 28566477 En línea : https://jasn.asnjournals.org/content/28/10/3055.long Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4079 Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children [documento electrónico] / Gloria Patricia Monsalve Arias, . - 2017.
Obra : Journal of The American Society of Nephrology
Idioma : Inglés (eng)
Palabras clave : Children immunosuppression nephrotic syndrome outcomes podocytopathies steroid resistance Resumen : We investigated the value of genetic, histopathologic, and early treatment response information in prognosing long-term renal outcome in children with primary steroid-resistant nephrotic syndrome. From the PodoNet Registry, we obtained longitudinal clinical information for 1354 patients (disease onset at >3 months and Mención de responsabilidad : Agnes Trautmann, Sven Schnaidt, Beata S Lipska-Ziętkiewicz, Monica Bodria, Fatih Ozaltin, Francesco Emma, Ali Anarat, Anette Melk, Marta Azocar, Jun Oh, Bassam Saeed, Alaleh Gheisari, Salim Caliskan, Jutta Gellermann, Lina Maria Serna Higuita, Augustina Jankauskiene, Dorota Drozdz, Sevgi Mir, Ayse Balat, Maria Szczepanska, Dusan Paripovic, Alexandra Zurowska, Radovan Bogdanovic, Alev Yilmaz, Bruno Ranchin, Esra Baskin, Ozlem Erdogan, Giuseppe Remuzzi, Agnieszka Firszt-Adamczyk, Elzbieta Kuzma-Mroczkowska, Mieczyslaw Litwin, Luisa Murer, Marcin Tkaczyk, Helena Jardim, Anna Wasilewska, Nikoleta Printza, Kibriya Fidan, Eva Simkova, Halina Borzecka, Hagen Staude, Katharina Hees, Franz Schaefer, PodoNet Consortium Referencia : J Am Soc Nephrol. 2017 Oct;28(10):3055-3065. DOI (Digital Object Identifier) : 10.1681/ASN.2016101121 PMID : 28566477 En línea : https://jasn.asnjournals.org/content/28/10/3055.long Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4079 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000688 AC-2017-077 Archivo digital Producción Científica Artículos científicos Disponible
Título : Congenital orbital teratoma, case report Otros títulos : Teratoma orbitario congénito, informe de caso Tipo de documento : documento electrónico Autores : Gloria I. Salazar, ; Gloria Patricia Monsalve Arias, Fecha de publicación : 2012 Títulos uniformes : Colombia Médica Idioma : Inglés (eng) Palabras clave : Orbit teratoma eye enucleation Resumen : Orbital teratoma is a rare tumor composed of tissue derived from the three germinal layers, it usually occurs in otherwise healthy newborns as a fluctuating mass in orbit, with extreme proptosis and periorbital deformity. There are few reports in literature about this topic; we present a case report with severe stretching and deformity of periocular tissue, which underwent enucleation and careful removal of the tumor, properly sparing the eyelids and other structures in the anophthalmic cavity to fit an ocular prosthesis. It did well, improving the patient’s cosmetic appearance and preserving his orbitofacial development. Even though in many cases it is not possible to preserve visual function in patients with congenital orbital teratoma, it is equally important to achieve the best possible cosmetic result. Mención de responsabilidad : Cristina González, Carlos A Restrepo, Gloria I Salazar, Patricia Monsalve Referencia : Colomb Med. 2012; 43: 82-5. DOI (Digital Object Identifier) : 10.25100/cm.v43i1.1062 Derechos de uso : CC BY En línea : https://colombiamedica.univalle.edu.co/index.php/comedica/article/view/1062 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3596 Congenital orbital teratoma, case report = Teratoma orbitario congénito, informe de caso [documento electrónico] / Gloria I. Salazar, ; Gloria Patricia Monsalve Arias, . - 2012.
Obra : Colombia Médica
Idioma : Inglés (eng)
Palabras clave : Orbit teratoma eye enucleation Resumen : Orbital teratoma is a rare tumor composed of tissue derived from the three germinal layers, it usually occurs in otherwise healthy newborns as a fluctuating mass in orbit, with extreme proptosis and periorbital deformity. There are few reports in literature about this topic; we present a case report with severe stretching and deformity of periocular tissue, which underwent enucleation and careful removal of the tumor, properly sparing the eyelids and other structures in the anophthalmic cavity to fit an ocular prosthesis. It did well, improving the patient’s cosmetic appearance and preserving his orbitofacial development. Even though in many cases it is not possible to preserve visual function in patients with congenital orbital teratoma, it is equally important to achieve the best possible cosmetic result. Mención de responsabilidad : Cristina González, Carlos A Restrepo, Gloria I Salazar, Patricia Monsalve Referencia : Colomb Med. 2012; 43: 82-5. DOI (Digital Object Identifier) : 10.25100/cm.v43i1.1062 Derechos de uso : CC BY En línea : https://colombiamedica.univalle.edu.co/index.php/comedica/article/view/1062 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3596 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000166 AC-2012-006 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2012-006.pdfAdobe Acrobat PDF