F. González

发表

Deletion of BCR region 3' in chronic myelogenous leukemia.

E. Anguita, A. Villegas, A. Mora, 2001, Cancer genetics and cytogenetics.

Presence of acute and chronic renal failure in patients with paroxysmal nocturnal hemoglobinuria: results of a retrospective analysis from the Spanish PNH Registry

S. Brunet, A. Gaya, B. Arrizabalaga, 2017, Annals of Hematology.

[HFE gene mutations, hepatic iron content, and histological severity in hepatitis C virus-induced chronic hepatitis].

C. Taxonera, M. Díaz‐Rubio, J. Ladero, 2003, Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva.

Characterization of a New α-Thalassemia-1 Mutation in a Spanish Family

D. Espinós, A. Villegas, F. González, 1989 .

Occurrence of BCR-ABL rearrangement in a Philadelphia chromosome-negative patient with 5q and 13q deletions and myeloproliferative syndrome.

E. Anguita, M. Ferrò, A. Villegas, 1998, Cancer genetics and cytogenetics.

Nondeletional α‐thalassemia in a Spanish population

A. Villegas, F. González, J. Sanchez, 1997 .

Erythropoietin plus granulocyte colony-stimulating factor in the treatment of myelodysplastic syndromes. Identification of a subgroup of responders. The Spanish Erythropathology Group.

J. Juncà, L. Font, L. Laurenti, 1999, Haematologica.

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

M. Mateo, P. Ropero, O. Briceño, 2007, Annals of Hematology.

Novel nonsense mutation in the α1-globin gene [HBA1:C.49A>T] is responsible for non-deletion α-thalassemia.

P. Ropero, A. Villegas, F. González, 2019, Clinical biochemistry.

Association of t(9;11)-MLL AF9 and trisomy 8 in an AML-M5 preceded by pancytopenia.

E. Anguita, M. Ferrò, E. del Potro, 2000, Cancer genetics and cytogenetics.

Cleavage of the ALL1 gene in acute lymphoid leukemia before treatment disappears in relapse.

E. Anguita, G. Saglio, A. Villegas, 1999, Haematologica.

Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in a cohort of 1,000 neonates in Madrid (Spain)

M. Mateo, P. Ropero, O. Briceño, 2006, Annals of Hematology.

THE THALASSEMIA SYNDROMES: MOLECULAR CHARACTERIZATION IN THE SPANISH POPULATION

E. Anguita, D. Espinós, P. Ropero, 2001, Hemoglobin.

Acute promyelocytic leukemia relapse in the central nervous system during hematologic and molecular remission

F. Lo Coco, E. Anguita, A. Villegas, 1999, American journal of hematology.

Abnormally low HbA1c secondary to hemoglobin J-Baltimore [beta 16(A13) Gly-->Asp]. Family study.

M. Gargallo, A. Villegas, F. González, 2010, Endocrinologia y nutricion : organo de la Sociedad Espanola de Endocrinologia y Nutricion.

Development and validation of a multivariable prediction rule for detecting a severe acquired ADAMTS13 activity deficiency in patients with thrombotic microangiopathies

P. Ropero, A. Villegas, M. Fuentes, 2017, Clinical chemistry and laboratory medicine.

Hb Nunobiki (α 2 141(HC3) Arg→Cys; HBA2:c.424C>T) in Spain: Mutation de novo or Acquired?

P. Ropero, A. Villegas, F. González, 2013 .

Association in Cis of the Mutations +20 (C>T) in the 5′ Untranslated Region and IVS-II-745 (C>G) on the β-Globin Gene

Á. Cervera, C. Beléndez, P. Ropero, 2013, Hemoglobin.

Hemoglobina Stanleyville II [ α78(EF7)Asn → Lys]. Primer caso descrito en España

P. Ropero, A. Villegas, F. González, 2008 .

First Spanish Case Of Thalassemia Major Due to a Compound Heterozygosity for the IVS-II-848 (C→A) And Codon 39 (C→T) Mutations Of The β-Globin Gene

P. Ropero, O. Briceño, A. Villegas, 2006, Hemoglobin.

Late relapse in BCR/ABL-positive patients after non-intensive chemotherapy

E. Anguita, A. Villegas, F. González, 1998, Leukemia.

The utility of multiparametric seven‐color flow cytometry in the detection of double hit lymphoma in ascitic fluid samples

P. Llamas, F. Cava, R. Cordoba, 2016, Cytometry. Part B, Clinical cytometry.

Haemoglobinopathies that occur with decreased HbA2 levels: a gene mutation set involving the δ gene at a Spanish centre

P. Ropero, A. Villegas, F. González, 2016, Journal of Clinical Pathology.

Capillary electrophoresis and mutational images of hemoglobin sendagi [Β42 (CD1) PHE → VAL; HBB: C.127T→G].

R. Díez, P. Ropero, C. Rodríguez-Vigil, 2019, Clinical biochemistry.

Delta0-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A2 levels

P. Ropero, A. Villegas, F. González, 2015 .

The First Case of Hb E-Saskatoon Associated with Hb Lepore-Baltimore Found in Spain

P. Ropero, A. Villegas, F. González, 2005, Hemoglobin.

The first report of a Philadelphia chromosome and BCR/ABL rearrangement positive myeloproliferative disorder in a child with thrombocythemia

E. Anguita, M. Ferrò, A. Villegas, 1998, Leukemia.

Two new mutations in cis on Gγ chain of fetal hemoglobin: Hb F-Madrid [Gγ50(D1)Ser→Cys] and [Gγ75(E19)Ile→Thr]

F. González, Á. Nogales, L. Villar, 2003, Annals of Hematology.

Hb Santander [β34(B16)Val→Asp (GTC→GAC)]: A New Unstable Variant Found as a De Novo Mutation in a Spanish Patient

E. Rodrigo, M. Mateo, P. Ropero, 2003, Hemoglobin.

A NOVEL SPLICE ACCEPTOR SITE MUTATION OF THE α2-GLOBIN GENE CAUSING α-THALASSEMIA

N. Noguera, A. Villegas, F. González, 2001 .

The importance of molecular screening of 11q23 abnormalities in childhood acute lymphoblastic leukemia: has the t(11;19)(q23;p13) a higher frequency than that revealed by conventional cytogenetic techniques?

E. Anguita, A. Villegas, F. González, 1998, Medical and pediatric oncology.

Study of the BCR/ABL rearrangement in patients with two Philadelphia chromosomes.

M. Ferrò, M. Resino, A. Villegas, 1993, Cancer genetics and cytogenetics.

Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]

A. Villegas, S. Rochas, F. González, 2022, Hemoglobin.

Thrombosis and severe asthenia as priority manifestations in paroxysmal nocturnal haemoglobinuria

A. Villegas, F. González, E. Fontanes, 2012, Annals of Hematology.

Hb Palencia: a novel δβδ-type two-way fusion variant with β-globin-like expression levels

J. Alonso, P. Ropero, A. Villegas, 2018, Journal of Clinical Pathology.

Characterization of deletional and non-deletional alpha globin variants in a large cohort from Spain between 2009 and 2014

P. Ropero, A. Villegas, F. González, 2019, Annals of Hematology.

Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies.

Á. Cervera, J. Anguita, P. Ropero, 2015, Clinical biochemistry.

Heterozygosity for deletion of hypersensitive site 3 in the human locus control region has an unexpected minor effect on red cell phenotype

P. Ropero, A. Villegas, F. González, 2014, Journal of Human Genetics.

16189 Mitochondrial variant and iron overload

P. Ropero, A. Villegas, F. González, 2007, Annals of Hematology.

Emerging hematological targets and therapy for cardiovascular disease: From bench to bedside

S. Redondo, A. Villegas, F. González, 2008, Biologics : targets & therapy.

Another Hb with inclusion bodies β-thalassemia, owing to Hb Durham-N.C. [β114(G16) Leu > Pro]. First case described in Hispanic populations

M. Morado, R. Cordoba, P. Ropero, 2012, Annals of Hematology.

Etiopathological mechanisms and clinical characteristics of hyperhemolysis syndrome in Spanish patients with thalassemia

G. Gervasini, J. Vagace, M. D. de la Maya, 2016, Annals of Hematology.

[Study of deferoxamine in subcutaneous profusion treatment of iron overload in myelodysplastic syndromes].

Á. Remacha, B. Arrizabalaga, A. Villegas, 2005, Medicina clinica.

Red blood cell phenotypes in alpha-thalassemias in the Spanish population.

B. Arrizabalaga, A. Villegas, F. González, 1998, Haematologica.

α‐thalassemia‐1 (— −‐CAL mutation) in a Spanish family

P. Ropero, A. Villegas, F. González, 1994, American journal of hematology.

Molecular characterization of a new family with α‐Thalassemia‐1 (——MA mutation)

D. Espinós, P. Ropero, A. Villegas, 1995, American journal of hematology.

Congenital dyserythropoietic anemia type III with unbalanced globin chain synthesis

P. Ropero, V. Furió, A. Villegas, 1994, European journal of haematology.

Bcl‐2 gene rearrangement: Diagnostic implications in a case of a large cell diffuse lymphoma appearing in leukemic phase

E. Anguita, A. Villegas, A. Villegas, 1995, American journal of hematology.

Usefulness of the rearrangement of the bcr/abl gene in extramedullary (lymph nodes) blast crisis diagnosed in chronic myeloid leukaemia

A. Villegas, F. González, P. Cabello, 1993, British journal of haematology.

Rearrangement of the BCR/ABL and TCR‐β genes in lymph node blast crisis diagnosed of chronic myeloid leukemia

A. Villegas, F. González, 1994, American journal of hematology.

Lymphoid blastic transformation in chronic myeloid leukemia

A. Villegas, F. González, B. Armada, 1994, American journal of hematology.

Erythrocytosis in a Child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] Associated with a Spanish (δβ)0-Thalassemia

C. Serí, C. Beléndez, P. Ropero, 2013, Hemoglobin.

Homozygous Constant Spring: the first case described in the west.

E. Anguita, N. Noguera, P. Ropero, 2000, Haematologica.

TEL/AML1 transcript and p16 gene deletion in a patient with childhood acute lymphoblastic leukaemia.

E. Anguita, A. Villegas, F. González, 1997, British Journal of Haematology.

Hb Extremadura [β64(E8)Gly→Ser;β133(H11)Val→Leu]: A New Molecular Analysis

P. Ropero, A. Villegas, F. González, 2011, Hemoglobin.

Hb AGENOGI [β90(F6)Glu→Lys] IN AN ARGENTINEAN GIRL

N. Noguera, A. Villegas, F. González, 2002, Hemoglobin.

[Association between hemoglobin Groene Hart and hemoglobin J-Paris-I: first case in Spain].

P. Ropero, A. Villegas, F. González, 2015, Medicina clínica (Ed. impresa).

Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia

J. Sevilla, P. Ropero, A. Villegas, 2014, International journal of hematology.

Characterization of a new hemoglobin variant: Hb Badalona (β31[B13]Leu→Val)

P. Ropero, A. Villegas, F. González, 2002, Annals of Hematology.

Identification of the Hb Lepore phenotype by HPLC.

E. Anguita, A. Villegas, P. Ropero, 1999, Haematologica.

Study of Three Families with Hb Agrinio [α29(B10)Leu→Pro, CTG>CCG (α2)] in the Spanish Population: Three Homozygous Cases

M. Baiget, I. Badell, P. Ropero, 2012, Hemoglobin.

[Prenatal diagnosis of hemoglobinopathies and thalassemias].

P. Ropero, Aurora Hernández, A. Villegas, 2009, Medicina clinica.

Detection of bcr/abl mRNA in a case of chronic myelogenous leukemia in long-term remission: CML or sensitivity of detection?

E. Anguita, E. del Potro, A. Villegas, 1998, Haematologica.

[The usefulness of the bcr/abl rearrangement in the diagnosis and evolution of chronic myeloid leukemia].

M. Ferrò, E. del Potro, A. Villegas, 1993, Medicina clínica (Ed. impresa).

Identification of a Novel Mutation in the β-Globin Gene 3′ Untranslated Region (HBB: c.*+118A > G) in Spain

P. Ropero, A. Villegas, F. González, 2015, Hemoglobin.

Molecular heterogeneity of β‐thalassaemia in a Spanish population from the area centre of Spain

P. Ropero, A. Villegas, F. González, 1996, European Journal of Haematology.

High incidence of the CD8/9 (+G) b0-thalassemia mutation in Spain

E. Anguita, P. Ropero, A. Villegas, 2005 .

Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene

P. Ropero, A. Villegas, F. González, 2020, Hemoglobin.

Frameshift CD 11 (-T) beta-thalassemia mutation.

A. Villegas, F. González, J. Sanchez, 1997, American journal of hematology.