Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gladys, Cossio"'
Autor:
Teresa, Chávez-Peña, Alejandra, Martínez-Camberos, Gladys, Cossio-Gurrola, Eliakym, Arámbula-Meraz, Indira, Herrera-Rodríguez, Enrique, Romo-Martínez, Noemi, García-Magallanes
Publikováno v:
Journal of genetics. 99
A relationship between the polymorphism in promoter region of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::710776f790deed48be7ffc5f3a9548a4
https://pubmed.ncbi.nlm.nih.gov/33622990
https://pubmed.ncbi.nlm.nih.gov/33622990
Autor:
Francisca Jaquez, Flávia Gameleira, Maira Graeff Burin, Joany Ramirez, Ceila Perez de Ferrán, Maria L. Castro Moreira, Ana Carolina Brusius-Facchin, Martha L. Solano Villareal, Simone Silva dos Santos Lopes, Kiyoko Abe Sandes, Hector P. Quintero Montano, Gladys Cossio, Heidy M. Barroso Sandoval, Francyne Kubaski, Kristiane Michelin-Tirelli, Paula F.V. de Medeiros, Sandra Leistner-Segal, Roberto Giugliani, Rodolfo Bareiro, Angelina Xavier Acosta
Publikováno v:
Molecular Genetics and Metabolism. 126:S87-S88
The mucopolysaccharidoses (MPS) include 11 rare disorders caused by deficiency of specific lysosomal enzymes resulting in the accumulation of undegraded glycosaminoglycans (GAGs) and several clinical consequences. The combined incidence for all MPS s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a73a1d8e7d0430cdb4ed595607a9161
https://doi.org/10.1016/j.ymgme.2018.12.216
https://doi.org/10.1016/j.ymgme.2018.12.216
Autor:
Luis Morales, Paul Gallardo, Gladys Cossio, Judith Hal, David Ellis, Alberto Bissot, Mireya de Rivas
Publikováno v:
Pharmacology & Pharmacy. :312-317
In the 1990s, misoprostol (synthetic prostaglandin E1 analogue) was found to be an effective abortive agent when taken orally and became widely used in Latin America as a means to terminate unwanted pregnancies. A variety of congenital anomalies have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::348ededcadacc9e4db9a3bd08b903bfa
https://doi.org/10.4236/pp.2013.43045
https://doi.org/10.4236/pp.2013.43045
Autor:
Darío Acuña-Castroviejo, Belgica Moreno, Iryna Rusanova, Luis C. López, Rosaura G. De Borace, Mariam Chahboune, Gladys Cossio, Tomás A. Diez, Germaine Escames
Publikováno v:
European Journal of Haematology. 85:529-537
Objective: To correlate the clinical and hematological features of β-globin gene haplotypes with the oxidative stress status in pediatric patients with sickle cell disease (SCD). Methods: A total of 95 patients with SCD and 40 healthy children were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69e1bfc274adb037a1d3b93e75ed0ead
https://doi.org/10.1111/j.1600-0609.2010.01528.x
https://doi.org/10.1111/j.1600-0609.2010.01528.x
Autor:
Mauricio Perea, Iryna Rusanova, Belgica Moreno, Germaine Escames, Darío Acuña-Castroviejo, F. Javier Perea, Gladys Cossio, Rosaura G. De Borace
Publikováno v:
American journal of human biology : the official journal of the Human Biology Council. 23(3)
Objective: To analyze the frequency of the haplotypes of β-globin gene cluster in randomly selected patients withsickle cell disease (SCD), attended in the Children's Hospital of Panama. Methods: Five polymorphic sites in the β-globin gene cluster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ef39ee984d59ffc2d00653b7b7e55df
https://pubmed.ncbi.nlm.nih.gov/21387457
https://pubmed.ncbi.nlm.nih.gov/21387457
Autor:
Iryna, Rusanova, Germaine, Escames, Gladys, Cossio, Rosaura G, de Borace, Belgica, Moreno, Mariam, Chahboune, Luís C, López, Tomas, Díez, Dario, Acuña-Castroviejo
Publikováno v:
European journal of haematology. 85(6)
To correlate the clinical and hematological features of β-globin gene haplotypes with the oxidative stress status in pediatric patients with sickle cell disease (SCD).A total of 95 patients with SCD and 40 healthy children were studied. The β-globi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86a26dd3e4619f58b92fe1a18b1b5450
https://pubmed.ncbi.nlm.nih.gov/20846340
https://pubmed.ncbi.nlm.nih.gov/20846340
Autor:
Noemí García-Magallanes, Maribel Aguilar-Medina, Juan José Araúz, Gladys Cossio de Gurrola, Eliakym Arámbula Meraz, Elfilda Durán, Gerardo Vaca Pacheco, Rosalío Ramos-Payán
Publikováno v:
Journal of Medical Case Reports, Vol 2, Iss 1, p 146 (2008)
Journal of Medical Case Reports
Journal of Medical Case Reports
Introduction Glucose-6-phosphate dehydrogenase deficiency is an X-linked recessive disease that causes acute or chronic hemolytic anemia and potentially leads to severe jaundice in response to oxidative agents. This deficiency is the most common huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbba03b659695daa2214006b680060aa
https://doi.org/10.1186/1752-1947-2-146
https://doi.org/10.1186/1752-1947-2-146
Autor:
de Gurrola GC; Servicio de Genética, Hospital del Niño de Panamá, Panamá. gcossio@cableonda.net, Araúz JJ, Durán E, Aguilar-Medina M, Ramos-Payán R, García-Magallanes N, Pacheco GV, Meraz EA
Publikováno v:
Journal of medical case reports [J Med Case Rep] 2008 May 06; Vol. 2, pp. 146. Date of Electronic Publication: 2008 May 06.