Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Luz Karime, Yunis"'
Autor:
Cynthia Rucinski, Luz Karime Yunis, Fernando Rosas, David Santacruz, Juan Manuel Camargo, Juan José Yunis
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Background Clinical and molecular diagnosis of inherited cardiac conditions is key to find at‐risk subjects and avoid preventable deaths. This study aimed to identify genetic variants in a sample of Colombian patients diagnosed with inheri
Externí odkaz:
https://doaj.org/article/27b0de40df78427b8d01eb4298568606
Autor:
Cindy Martinez, Luz Karime Yunis, Edgar Cabrera, Johnny García, Gloria Uribe, Edna Quintero, Juan Jose Yunis, Adriana Linares Ballesteros, Isabel Cristina Sarmiento
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 1, Pp 1-3 (2022)
Cyclin dependent kinase inhibitor (CDKN) 2A/B deletion is correlated with poor risk factors, such as high blood cell count, higher rate of induction therapy failure, and earlier relapses in pediatric patients with acute lymphoblastic leukemia (ALL).
Externí odkaz:
https://doaj.org/article/a2216a2ee71e420c806703427e1286ac
Autor:
Adriana Linares Ballesteros, Luz Karime Yunis, Johnny García, Nelson Aponte, Jessica Flechas, Cindy Martinez, Gloria Uribe, Edna Quintero, Angela Díaz, Carlos Pardo, Isabel Cristina Sarmiento, Agustin Contreras, Juan Jose Yunis
Publikováno v:
Cancer Reports, Vol 5, Iss 5, Pp n/a-n/a (2022)
Abstract Background Philadelphia‐like (Ph‐like) acute lymphoblastic leukemia (ALL) is a subtype of pediatric leukemia with high risk factors and poor outcome. There are few reports of its prevalence in Latin America. Aim This study evaluated the
Externí odkaz:
https://doaj.org/article/653f5d1563f249b8bfb7cef7c6a4294d
Autor:
Diana Carolina Grajales-Ospina, Luz Karime Yunis-Hazbun, Andrés Mauricio Camacho-Montaño, Alejandro Antonio Bautista-Charry, Reinaldo Niño-Alba, Juan José Yunis
Publikováno v:
Revista de la Facultad de Medicina, Vol 71, Iss 2 (2022)
Introduction: Noninvasive prenatal testing (NIPT) is a screening test for fetal aneuploidy with higher specificity and sensibility rates compared to traditional biochemical prenatal screening. Objective: To evaluate concordance between NIPT and pren
Externí odkaz:
https://doaj.org/article/2bc887c1d6d34f40b0797c4c83126e68
Publikováno v:
Genetics and Molecular Biology, Vol 41, Iss 4, Pp 750-757 (2018)
Abstract Hemophilia A (HA) is an X-linked recessive disorder and the second most common coagulation disorder with an incidence of 1 in 5,000 live born males. Worldwide, there are 178,500 affected individuals, 60% with the severe form of the disease.
Externí odkaz:
https://doaj.org/article/e90cc0e35e4d4ea69b50d964d00f655a
Autor:
Luz Karime Yunis Hazbun, Yolima Andrea Parrado Jara, Teresa Adriana Linares Ballesteros, Gisela Barros, Gloria Uribe Botero, Edna Margarita Quintero Canasto, Lina Eugenia Jaramillo Barberi, Jaime José Pérez, Leila Martínez, Juan José Yunis Londoño
Publikováno v:
Revista Colombiana de Hematología y Oncología. 8:187-188
Objetivo: caracterizar las alteraciones genómicas (cromosómicas y moleculares) identificadas en pacientes pediátricos con diagnóstico de leucemia mieloide aguda y sus patrones de coocurrencia, con miras a identificar factores pronósticos y event
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49ffee3cd066d26dfb798ed3bc8fcd73
https://doi.org/10.51643/22562915.478
https://doi.org/10.51643/22562915.478
Autor:
Adriana Teresa Linares Ballesteros, Johnny Francisco García Medina, Luz Karime Yunis Hazbun, Gloria Inés Uribe Botero, Juan José Yunis Londoño, Edna Margarita Quintero Canasto, Nelson Hernando Aponte Barrios, Cindy Nathalie Martínez Gutiérrez, Jessica Flechas Afanador, Ángela María Díaz
Publikováno v:
Revista Colombiana de Hematología y Oncología. 8:191-192
Introducción: la leucemia linfoblástica aguda de precursores B (LLA-B) es la neoplasia más frecuente en la infancia. Las alteraciones genéticas más comunes en niños son t(12;21), t(4;11) y Philadelphia-like (Ph-like). El estudio de estas altera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8f2f67aa8f827fae3487083ef8c1707
https://doi.org/10.51643/22562915.481
https://doi.org/10.51643/22562915.481
Autor:
Johnny García, Adriana Linares Ballesteros, Gloria Inés Uribe, Isabel Sarmiento, Angela Díaz, Carlos Pardo, Juan J. Yunis, Nelson Aponte, Jessica Flechas, Luz Karime Yunis, Cindy Martinez, Edna Quintero, Agustin Contreras
Publikováno v:
Cancer reports (Hoboken, N.J.). 5(5)
BACKGROUND Philadelphia-like (Ph-like) acute lymphoblastic leukemia (ALL) is a subtype of pediatric leukemia with high risk factors and poor outcome. There are few reports of its prevalence in Latin America. AIM This study evaluated the frequency and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3fda2995a1131f0940f797d3209e644
https://pubmed.ncbi.nlm.nih.gov/34787376
https://pubmed.ncbi.nlm.nih.gov/34787376
Autor:
Milena, Villamil-Osorio, Luz Karime, Yunis, Ligia, Quintero, Sonia, Restrepo-Gualteros, Juan José, Yunis, Lina, Jaramillo, Bertha Inés, Agudelo, Yaqueline, Ladino
Publikováno v:
Andes pediatrica : revista Chilena de pediatria. 92(6)
In newborns with respiratory failure and interstitial lung disease, it should be approached as chILD (Childhood Interstitial Lung Disease) syndrome to rule out alterations in surfactant metabolism and brain-lung-thyroid syndrome caused by pathogenic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cba35642ad8fd48c9c43abda23065dc2
https://pubmed.ncbi.nlm.nih.gov/35506806
https://pubmed.ncbi.nlm.nih.gov/35506806
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 5, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 5, Pp n/a-n/a (2020)
Background Hemophilia B (HB) is a coagulation disorder with an X‐linked recessive inheritance pattern, caused by plasma FIX deficiency. In Colombia, HB is considered a rare and high‐cost disease, with 362 males reported in 2017. Methods Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12e908b08f47acea8ef2c5c8fa0fd25f
http://europepmc.org/articles/PMC7216803
http://europepmc.org/articles/PMC7216803