Incidence of the HFE gene mutations in a cohort of non-Spanish origin neonates in Madrid

被引:2
|
作者
Ropero, Paloma [1 ]
Llorente, Leopoldo [1 ]
Gonzalez, Fernando A. [1 ]
Briceno, Olga [1 ]
Mateo, Marta [1 ]
Polo, Marta [1 ]
Villegas, Ana [1 ]
机构
[1] Hosp Clin San Carlos, Serv Hematol & Hemoterapia, E-28040 Madrid, Spain
关键词
D O I
10.1007/s00277-007-0264-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:459 / 462
页数:4
相关论文
共 50 条
  • [31] 284 Comparison of Molecular Mutations of G6Pd Gene Between Icteric and Non Icteric Neonates
    Zahed Y Pasha
    Ahmadpour M Kacho
    Akha H Van Niaky
    R Farhadi
    Pediatric Research, 2010, 68 (Suppl 1) : 146 - 146
  • [32] Cohort and age of onset analysis of female breast cancer in non-Spanish surnamed Whites and three Asian ethnic groups in Los Angeles County, from 1975 to 1999.
    Corey, BA
    Setyawan, J
    Yu, YF
    Weitzel, JN
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 368 - 368
  • [33] Novel And Recurrent Mutations In NLRP3 Gene Encoding Cryopyrin in Patients With Cryopyrinopathies: Experience from a Spanish Cohort
    Pascal, Mariona
    Ignacio Arostegui, Juan
    Modesto, Consuelo
    Arguelles, Federico
    Cinta Cid, Maria
    Antonia Gonzalez-Ensenat, Maria
    Ramos, Eduardo
    Garcia-Consuegra, Julia
    Bou, Rosa
    Molero, Xavier
    Calvo, Inmaculado
    Luz Gamir, Maria
    Anton, Jordi
    Arnal, Cristina
    Vargas, Carmen
    Cabades, Francisco
    Sol Camacho, Mari
    Plaza, Susana
    Rius, Josefina
    Yaguee, Jordi
    Juan, Manel
    CLINICAL IMMUNOLOGY, 2009, 131 : S147 - S148
  • [34] LGMD2H patients of non Hutterite origin with mutations in TRIM32 gene
    Saccone, V.
    Scutifero, M.
    Palladino, A.
    Di Gregorio, M. G.
    Ventriglia, V. M.
    Piluso, G.
    Canki-Klain, N.
    Nigro, V.
    Politano, L.
    NEUROMUSCULAR DISORDERS, 2008, 18 (9-10) : 817 - 817
  • [35] Correlation between HFE gene mutations and ALT levels may increase cardiovascular disease risk in patients with non-alcoholic steatohepatitis NASH
    Kruger, C.
    Kotze, M.
    SAMJ SOUTH AFRICAN MEDICAL JOURNAL, 2012, 102 (08): : 705 - +
  • [36] Genetic analysis of the C1INH gene in the Spanish HAE population reveals a high incidence of mutations in exon 3
    Roche, O
    Blanch, A
    Fontán, G
    López-Trascasa, M
    MOLECULAR IMMUNOLOGY, 2003, 40 (2-4) : 222 - 222
  • [37] Mutations in the Connexin-26 gene in Spanish and Cuban families with autosomal recessive non-syndrome hearing loss
    Uriarte, A
    Villamar, M
    del Castillo, I
    Romero, L
    Moreno, F
    EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 169 - 169
  • [38] Absence of Microcephalin Gene Mutations in a Large Cohort of Non-Consanguineous Patients With Autosomal Recessive Primary Microcephaly
    Scala, Iris
    Titomanlio, Luigi
    Del Giudice, Ennio
    Passemard, Sandrine
    Figliuolo, Chiara
    Annunziata, Patrizia
    Granese, Barbara
    Scarpato, Elena
    Verloes, Alain
    Andria, Generoso
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (11) : 2882 - 2885
  • [39] Novel mutations in the bone morphogenetic protein 6 gene in patients with iron overload and non-homozygous genotype for the HFE p.Cys282Tyr mutation
    Alvarenga, Aline Morgan
    da Silva, Nathalia Kozikas
    Silva Fonseca, Paula Fernanda
    Oliveira, Theo G. M.
    da Silva Monteiro, Jacilene Barbosa
    Cancado, Rodolfo Delfini
    Naoum, Flavio Augusto
    Dinardo, Carla Luana
    Brissot, Pierre
    Lima Santos, Paulo Caleb Junior
    BLOOD CELLS MOLECULES AND DISEASES, 2020, 84
  • [40] Clinicopathological Features of Breast Cancer in 149 Patients with Non-BRCA Gene Mutations: A Single Institutional Cohort Study
    Yu, Qing
    Heller, Melissa
    Mehr, Chelsea
    LABORATORY INVESTIGATION, 2025, 105 (03)