Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anabel Arends"'
Publikováno v:
Revista Digital de Postgrado, Vol 12, Iss 2 (2023)
El folato es un miembro del grupo de la vitamina B y está relacionado con enfermedades crónicas como anemia megaloblástica, enfermedad cardiovascular, cáncer, disfunción cognitiva y riesgo de defectos del tubo neural. La proteína 5,10- metilent
Externí odkaz:
https://doaj.org/article/2e4ec5653f574a02974fab24d1f009f3
Autor:
Anabel Arends, Miguel Marrero, Airene Dictamen, Raul Ferreira, Yelitza Zambrano, Anna Chiarello, Maritza Alvarez, Francys Escobar
Publikováno v:
Forensic Science International: Genetics Supplement Series. 1:303-305
Fifteen autosomal markers (CSF1PO, TH01, TPOX, F13A01, FESFPS, VWA, D16S539, D7S820, D13S317, D5S818, D3S1358, D8S1179, LPL, F13B and D1S80) were evaluated in the Central Region of Venezuela (States of Aragua, Carabobo and Cojedes) in order to test t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fd946e75afffb30d37eda98196fed25
https://doi.org/10.1016/j.fsigss.2007.10.072
https://doi.org/10.1016/j.fsigss.2007.10.072
Autor:
Nathalie Gérard, Anabel Arends, Odalis García, Omar Castillo, Gilberto Gómez, Martha Bravo-Urquiola, Tsouria Berbar, Gloria García, Marycarmen Chacín, Dalia Velasquez, Rajagopal Krishnamoorthy, Silvia Montilla
Publikováno v:
Hemoglobin. 36(3)
In order to establish the spectrum of β-thalassemia (β-thal) mutations in the Venezuelan population for the first time, 127 unrelated subjects either with a suspicion of β-thal trait or with a clinically recognized β-thal syndrome of different de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0447ff0d465818453f54b6def5f6937f
https://pubmed.ncbi.nlm.nih.gov/22563936
https://pubmed.ncbi.nlm.nih.gov/22563936
Autor:
Anabel Arends Dr, Omar Castillo, Maritza Alvarez, Tibisay Arends De O, Marycarmen Chacín, José M Guevara, Martha Bravo-Urquiola
Publikováno v:
Annals of human biology. 35(2)
Several previous studies reported that the Venezuelan Warao Indians presented unusual genetic characteristics.The present study checked previous reports of a high frequency of hereditary persistence of fetal hemoglobin (HPFH) and examined other hemat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99e21c8865614ed5fc8cfbad269c98e5
https://pubmed.ncbi.nlm.nih.gov/18428016
https://pubmed.ncbi.nlm.nih.gov/18428016
Autor:
Martha, Bravo-Urquiola, Anabel, Arends, Silvia, Montilla, José María, Guevara-I, Gloria, García, Maritza, Alvarez, Omar, Castillo
Publikováno v:
Investigacion clinica. 47(2)
The propositus is a two year old child with a severe hemolytic anemia and increased level of Hb F. The Hbs A, A2 and F were eluted and quantitated by cation exchange high-performance liquid chromatography (HPLC-CE). DNA was isolated from peripheral b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5c114b8f21e7c4656ff51a521156097
https://pubmed.ncbi.nlm.nih.gov/16886779
https://pubmed.ncbi.nlm.nih.gov/16886779
Autor:
Martha, Bravo-Urquiola, Anabel, Arends, Silvia, Montilla, Dalia, Velásquez, Gloria, Garcìa, Maritza, Alvarez, José, Guevara, Omar, Castillo
Publikováno v:
Investigacion clinica. 45(4)
The hemoglobinopathies are a very heterogeneous group of congenital hemolytic anemias, which includes hemoglobin (Hb) variants, thalassemia and hereditary persistence of fetal hemoglobin (HPFH). The aim of this study was to determine the frequency of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d2b2e1750a9c7e363d5c7cdc276471fb
https://pubmed.ncbi.nlm.nih.gov/15602897
https://pubmed.ncbi.nlm.nih.gov/15602897
Autor:
martha Bravo Urquiola, L Dalia Velásquez De, Natalie Gerard, Gloria García Lic, Rajagapol Krishnamoorthy, Silvia Montilla, Anabel Arends, Maritza Alvarez
Publikováno v:
Blood. 104:3728-3728
Hereditary Persistence of Fetal Hemoglobin (HPFH) is a clinically benign condition characterized by continuous synthesis of fetal hemoglobin (Hb F) in adult life without major related hematological changes. The nondeletional HPFH is characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe0b07a41918140094032e9181779fb2
https://doi.org/10.1182/blood.v104.11.3728.3728
https://doi.org/10.1182/blood.v104.11.3728.3728
Autor:
Anabel Arends-Merino, J. Wasserman, Claudio Ogier, Richardo Giscombe, Anne-Marie Sjörgen, Peter Reizenstein
Publikováno v:
Cancer Immunology Immunotherapy. 14
Lymphocyte response to mitogens and to lymphocyte suppressor and monocyte helper activity was studied in 18 patients with acute myeloid leukemia in complete remission, and in 17 healthy controls. Ten patients were maintained with chemotherapy alone (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4c8763492a30d5aa9c7d8bd9bbc4968
https://doi.org/10.1007/bf00199429
https://doi.org/10.1007/bf00199429