Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ricardo Hojas"'
Autor:
Jorge Larrondo, Javiera Donoso, Gonzalo Correa, Jaime Álvarez, Ricardo Valjalo, Carmen Vergara, Álvaro Ríos, Ricardo Hojas, Christine Rojas, José Tomás Gonzalez, Camila Peña, Hernán López-Vidal, Carolina Contreras, Pablo Soto
Publikováno v:
Revista médica de Chile v.147 n.10 2019
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: Immunoglobulin light chain (AL) amyloidosis is a rare and underdiagnosed entity. Aim: To characterize patients with AL amyloidosis in Chilean public health centers. Material and Methods: We conducted a retrospective, multicenter study. Pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23af00684e192f6ee88bc1042b70526d
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019001001239
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872019001001239
Autor:
Marta Mateo, Celina Benavente, Ana Villegas, Guillermo Martin, Paloma Ropero, Fernando A. González, Ricardo Hojas, Marta Polo, María Salvador
Publikováno v:
Hemoglobin. 29:113-117
We describe, in a Spanish family with moderate microcytosis and hypochromia, a novel nondeletional α-thalassemia (thal) mutation localized on the α2-globin gene. DNA sequencing revealed a point mutation at codon 125 (CTG→CGG) in the heterozygous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c09dcaa4da9796422723767e2e3f22f2
https://doi.org/10.1081/hem-200058578
https://doi.org/10.1081/hem-200058578
Publikováno v:
Hemoglobin. 27:185-190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2defff27403ab2d3889defd95cdf1683
https://doi.org/10.1081/hem-120023383
https://doi.org/10.1081/hem-120023383
Autor:
C. José, Ricardo Hojas, C. Garcia, F. Valverde, Ana Villegas, A. Nogales, L. Villar, Fernando A. González, Paloma Ropero
Publikováno v:
Annals of Hematology. 82:181-183
We describe a new structural hemoglobin variant of Gγ with two amino acid replacements in cis found in the umbilical cord blood of a neonate in Madrid, Spain. The substitutions were identified on exon 2 of the Gγ globin gene, at codon 50 (TCT→TGT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::566a62089a50d04dce1f972bf54d29b6
https://doi.org/10.1007/s00277-002-0598-5
https://doi.org/10.1007/s00277-002-0598-5
Autor:
Guillermo, Martin, Ana, Villegas, Fernando Ataulfo, González, Paloma, Ropero, Ricardo, Hojas, Marta, Polo, Marta, Mateo, Maria, Salvador, Celina, Benavente
Publikováno v:
Hemoglobin. 29(2)
We describe, in a Spanish family with moderate microcytosis and hypochromia, a novel nondeletional alpha-thalassemia (thal) mutation localized on the alpha2-globin gene. DNA sequencing revealed a point mutation at codon 125 (CTG --CGG) in the heteroz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a436b9377727bd624a8e41be8342bf82
https://pubmed.ncbi.nlm.nih.gov/15921163
https://pubmed.ncbi.nlm.nih.gov/15921163
Publikováno v:
Hemoglobin. 27(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9f99d4c3c2ec0ab98664ebaa693aa02
https://pubmed.ncbi.nlm.nih.gov/12908804
https://pubmed.ncbi.nlm.nih.gov/12908804