GIRELLI, Domenico
GIRELLI, Domenico
DIPARTIMENTO DI MEDICINA
["Hyperferritinemia-cataract syndrome". Description of a new hereditary disease, from anamnesis to molecular diagnosis]
1997-01-01 Girelli, Domenico; P., Piccoli; Corrocher, Roberto
[Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy]
1993-01-01 Pacor, Maria Luisa; Biasi, Domenico; Girelli, Domenico; P., Cortina; Corrocher, Roberto
[Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology]
1991-01-01 L., Vettore; M. C., De Mattels; E., Bonollo; V., De Angelis; F., Sorrentino; T., Trevisan; Guarini, Patrizia; Girelli, Domenico; Olivieri, Oliviero
[Genetic risk factors in ischemic cardiopathy]
2001-01-01 Girelli, Domenico; Martinelli, Nicola
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)]
1991-01-01 Olivieri, Oliviero; Girelli, Domenico; Corrocher, Roberto
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport
1992-01-01 Olivieri, Oliviero; Girelli, Domenico; Vettore, Luciano; Balercia, Giancarlo; Corrocher, Roberto
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.
2002-01-01 Friso, Simonetta; Choi, S. w.; Girelli, Domenico; Mason, J. b.; Dolnikoski, G. b.; Bagley, P. j.; Olivieri, Oliviero; Jacques, P. f.; Rosenberg, I. h.; Corrocher, Roberto; Selhub, A. j.
A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist
2017-01-01 Girelli, Domenico; Piubelli, Chiara; Martinelli, Nicola; Corrocher, Roberto; Olivieri, Oliviero
A Five-Step Vascular Ultrasound Examination in Heart Failure: The First Two Years of the "ABCDE" G-SIUMB Multicenter Study 2018-2022
2020-01-01 Mozzini, Chiara; Soresi, Maurizio; Pesce, Giancarlo; Girelli, Domenico
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract
1995-01-01 Girelli, Domenico; Olivieri, Oliviero; DE FRANCESCHI, Lucia; Corrocher, Roberto; G., Bergamaschi; M., Cazzola
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3
2001-01-01 Girelli, Domenico; Bozzini, C; Roetto, A; Daraio, F; Colombari, R; Corrocher, Roberto; Camaschella, C.
A Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone Levels
2020-01-01 Lira Zidanes, Acaynne; Marchi, Giacomo; Busti, Fabiana; Marchetto, Alessandro; Fermo, Elisa; Giorgetti, Alejandro; Vianello, Alice; Castagna, Annalisa; Olivieri, Oliviero; Bianchi, Paola; Girelli, Domenico
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.
2014-01-01 Shen, Gq; Girelli, Domenico; Li, L; Rao, S; Archacki, S; Olivieri, Oliviero; Martinelli, Nicola; Park, Je; Chen, Q; Topol, Ej; Wang, Qk
A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia
2011-01-01 Iacobucci, I; Sazzini, M; Garagnani, P; Ferrari, A; Boattini, A; Lonetti, A; Papayannidis, C; Mantovani, V; Marasco, E; Ottaviani, E; Soverini, S; Girelli, Domenico; Luiselli, D; Vignetti, M; Baccarani, M; Martinelli, G.
A single dialysis session of hemodiafiltration with sorbent-regenerated endogenous ultrafiltrate reinfusion (HFR) removes hepcidin more efficiently than bicarbonate hemodialysis: a new approach to containing hepcidin burden in dialysis patients?
2018-01-01 Tessitore, Nicola; Poli, Albino; Bedogna, Valeria; Corazza, Luca; Campostrini, Natascia; Atti, Mauro; Sereni, Luisa; Castagna, Annalisa; Girelli, Domenico; Pessolano, Giuseppina; Lupo, Antonio
A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis
2011-01-01 Girelli, Domenico; Trombini, P; Busti, Fabiana; Campostrini, Natascia; Sandri, Marco; Pelucchi, S; Westerman, M; Ganz, T; Nemeth, E; Piperno, A; Camaschella, C.
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism
2002-01-01 Friso, S.; Girelli, D.; Trabetti, E.; Stranieri, C.; Olivieri, O.; Tinazzi, E.; Martinelli, N.; Faccini, G.; Pignatti, P. F.; Corrocher, R.
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism
2002-01-01 Friso, Simonetta; Girelli, Domenico; Trabetti, Elisabetta; Stranieri, C; Olivieri, Oliviero; Tinazzi, Elisa; Martinelli, Nicola; Faccini, G; Pignatti, Pierfranco; Corrocher, Roberto
Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis
2019-01-01 Marchi, Giacomo; Busti, Fabiana; LIRA ZIDANES, Acaynne; Castagna, Annalisa; Girelli, Domenico
Acquired iron overload associated with antitransferrin monoclonal immunoglobulin: a case report.
2008-01-01 Gian Luca, Forni; Girelli, Domenico; Martina, Lamagna; Marco, Mori; Eugenio, Marinaro; Campostrini, Natascia; Paola, Carrara; Massimo, Maffei
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
["Hyperferritinemia-cataract syndrome". Description of a new hereditary disease, from anamnesis to molecular diagnosis] | 1-gen-1997 | Girelli, Domenico; P., Piccoli; Corrocher, Roberto | |
[Effectiveness of loratadine vs. placebo in the treatment of urticaria-angioedema syndrome in patients with food allergy] | 1-gen-1993 | Pacor, Maria Luisa; Biasi, Domenico; Girelli, Domenico; P., Cortina; Corrocher, Roberto | |
[Endogenous erythrocyte proteolysis: a new approach to the study of membrane physiopathology] | 1-gen-1991 | L., Vettore; M. C., De Mattels; E., Bonollo; V., De Angelis; F., Sorrentino; T., Trevisan; Guarini, Patrizia; Girelli, Domenico; Olivieri, Oliviero | |
[Genetic risk factors in ischemic cardiopathy] | 1-gen-2001 | Girelli, Domenico; Martinelli, Nicola | |
[Ion transport in erythrocytes: a universal physiological model. Reflections on the pathogenesis of hypertension (editorial)] | 1-gen-1991 | Olivieri, Oliviero; Girelli, Domenico; Corrocher, Roberto | |
A case of congenital dyserythopoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation transport | 1-gen-1992 | Olivieri, Oliviero; Girelli, Domenico; Vettore, Luciano; Balercia, Giancarlo; Corrocher, Roberto | |
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. | 1-gen-2002 | Friso, Simonetta; Choi, S. w.; Girelli, Domenico; Mason, J. b.; Dolnikoski, G. b.; Bagley, P. j.; Olivieri, Oliviero; Jacques, P. f.; Rosenberg, I. h.; Corrocher, Roberto; Selhub, A. j. | |
A decade of progress on the genetic basis of coronary artery disease. Practical insights for the internist | 1-gen-2017 | Girelli, Domenico; Piubelli, Chiara; Martinelli, Nicola; Corrocher, Roberto; Olivieri, Oliviero | |
A Five-Step Vascular Ultrasound Examination in Heart Failure: The First Two Years of the "ABCDE" G-SIUMB Multicenter Study 2018-2022 | 1-gen-2020 | Mozzini, Chiara; Soresi, Maurizio; Pesce, Giancarlo; Girelli, Domenico | |
A linkage between hereditary hyperferritinaemia not related to iron overload and autosomal dominant congenital cataract | 1-gen-1995 | Girelli, Domenico; Olivieri, Oliviero; DE FRANCESCHI, Lucia; Corrocher, Roberto; G., Bergamaschi; M., Cazzola | |
A new mutation in transferrin receptor 2 gene in hemochromatosis type 3 | 1-gen-2001 | Girelli, Domenico; Bozzini, C; Roetto, A; Daraio, F; Colombari, R; Corrocher, Roberto; Camaschella, C. | |
A Novel ALAS2 Missense Mutation in Two Brothers With Iron Overload and Associated Alterations in Serum Hepcidin/Erythroferrone Levels | 1-gen-2020 | Lira Zidanes, Acaynne; Marchi, Giacomo; Busti, Fabiana; Marchetto, Alessandro; Fermo, Elisa; Giorgetti, Alejandro; Vianello, Alice; Castagna, Annalisa; Olivieri, Oliviero; Bianchi, Paola; Girelli, Domenico | |
A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene. | 1-gen-2014 | Shen, Gq; Girelli, Domenico; Li, L; Rao, S; Archacki, S; Olivieri, Oliviero; Martinelli, Nicola; Park, Je; Chen, Q; Topol, Ej; Wang, Qk | |
A polymorphism in the chromosome 9p21 ANRIL locus is associated to Philadelphia positive acute lymphoblastic leukemia | 1-gen-2011 | Iacobucci, I; Sazzini, M; Garagnani, P; Ferrari, A; Boattini, A; Lonetti, A; Papayannidis, C; Mantovani, V; Marasco, E; Ottaviani, E; Soverini, S; Girelli, Domenico; Luiselli, D; Vignetti, M; Baccarani, M; Martinelli, G. | |
A single dialysis session of hemodiafiltration with sorbent-regenerated endogenous ultrafiltrate reinfusion (HFR) removes hepcidin more efficiently than bicarbonate hemodialysis: a new approach to containing hepcidin burden in dialysis patients? | 1-gen-2018 | Tessitore, Nicola; Poli, Albino; Bedogna, Valeria; Corazza, Luca; Campostrini, Natascia; Atti, Mauro; Sereni, Luisa; Castagna, Annalisa; Girelli, Domenico; Pessolano, Giuseppina; Lupo, Antonio | |
A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis | 1-gen-2011 | Girelli, Domenico; Trombini, P; Busti, Fabiana; Campostrini, Natascia; Sandri, Marco; Pelucchi, S; Westerman, M; Ganz, T; Nemeth, E; Piperno, A; Camaschella, C. | |
A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: Relationships with C677T polymorphism and homocysteine/folate metabolism | 1-gen-2002 | Friso, S.; Girelli, D.; Trabetti, E.; Stranieri, C.; Olivieri, O.; Tinazzi, E.; Martinelli, N.; Faccini, G.; Pignatti, P. F.; Corrocher, R. | |
A1298C methylentetrahydrofolate reductase mutation and coronary artery disease:relationship with C677T polymorphysm and homocystein/folate metabolism | 1-gen-2002 | Friso, Simonetta; Girelli, Domenico; Trabetti, Elisabetta; Stranieri, C; Olivieri, Oliviero; Tinazzi, Elisa; Martinelli, Nicola; Faccini, G; Pignatti, Pierfranco; Corrocher, Roberto | |
Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis | 1-gen-2019 | Marchi, Giacomo; Busti, Fabiana; LIRA ZIDANES, Acaynne; Castagna, Annalisa; Girelli, Domenico | |
Acquired iron overload associated with antitransferrin monoclonal immunoglobulin: a case report. | 1-gen-2008 | Gian Luca, Forni; Girelli, Domenico; Martina, Lamagna; Marco, Mori; Eugenio, Marinaro; Campostrini, Natascia; Paola, Carrara; Massimo, Maffei |