Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Eraso-Garnica, Ruth"'
Autor:
Quiñones-Rios, Lorena, Estévez Capacho, Mayra Alexandra, Niño Serna, Laura Fernanda, Hernández Zapata, Lady Johana, Eraso Garnica, Ruth María, Vélez Echeverri, Catalina, Baquero Rodríguez, Richard
Publikováno v:
In Revista Colombiana de Reumatologia October-December 2024 31(4):463-472
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Medina, Ana María, Calle, Mateo, Eraso-Garnica, Ruth, Peinado-Acevedo, Juan Sebastián, Vanegas-García, Adriana Lucía, Jaramillo-Arroyave, Daniel, Muñoz-Vahos, Carlos Horacio, Hernández-Zapata, Lady Johanna
Publikováno v:
Iatreia, Vol 35, Iss 2, Pp 108-116 (2022)
Objective: To describe the main demographic and clinical characteristics of patients who were diagnosed with childhood polyarteritis nodosa (PAN). Methods: A descriptive study was conducted using retrospective data. Results: The clinical registries
Externí odkaz:
https://doaj.org/article/7c3ee6b6cf434350bddac4130bc51f65
Publikováno v:
Iatreia, Vol 26, Iss 2, Pp 207-214 (2013)
Granulomatosis with polyangiitis as a cause of kidney-lung syndrome is uncommon in children. We report the case of a 13 year old patient with alveolar hemorrhage, rapidly progressive glomerulonephritis, episcleritis and anti PR3. We refer to features
Externí odkaz:
https://doaj.org/article/c294dd79eb4d492ea8c79660ef26cbd4
Autor:
Ramírez Campo, Lyna, Londoño Salinas, Ana María, Gómez Gómez, Lina Vanessa, Ruíz Suárez, Ana Cristina, Eraso Garnica, Ruth María
Publikováno v:
Revista Colombiana de Reumatología, Volume: 26, Issue: 4, Pages: 280-284, Published: 01 NOV 2020
Cutaneous mucinosis is a group of conditions characterized by the abnormal deposition of mucin in the skin. They can be primary, which in turn can be inflammatory-degenerative, and hamartomatous-neoplastic; or secondary. Papulonodular mucinosis is pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______618::488c0325c767d92bff141ebba14744d2
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-81232019000400280&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-81232019000400280&lng=en&tlng=en
Autor:
Medina, Ana María, Calle, Mateo, Eraso-Garnica, Ruth, Peinado-Acevedo, Juan Sebastián, Vanegas-García, Adriana Lucía, Jaramillo-Arroyav, Daniel, Muñoz-Vahos, Carlos Horacio, Hernández-Zapata, Lady Johanna
Publikováno v:
Iatreia; abr-jun2022, Vol. 35 Issue 2, p108-116, 9p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Hernández Zapata Lady, Velásquez Méndez Monica, Eraso Garnica Ruth, Álvarez-Olmos Martha I, Guarnizo Zucardi Pilar, Olmos Carlos, Rivera Carolina, Bautista Alaín, Franco Jose
Publikováno v:
Frontiers in Immunology. 6
Publikováno v:
Iatreia, Volume: 26, Issue: 2, Pages: 207-214, Published: APR 2013
La granulomatosis con poliangitis como causa del síndrome pulmón-riñón es infrecuente en niños. Presentamos el caso de un paciente de 13 años con hemorragia alveolar, glomerulonefritis rápidamente progresiva, escleritis y anticuerpos anti-PR3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______618::b5646b58e31b67bcf62949b43e6189c8
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-07932013000200009&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121-07932013000200009&lng=en&tlng=en
Publikováno v:
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
Universidad de Antioquia
instacron:Universidad de Antioquia
Granulomatosis with polyangiitis as a cause of kidney-lung syndrome is uncommon in children. We report the case of a 13 year old patient with alveolar hemorrhage, rapidly progressive glomerulonephritis, episcleritis and anti PR3. We refer to features
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::db4e462fb9e9d9bba8bb6399e62d917f