GIRELLI, Domenico

GIRELLI, Domenico  

DIPARTIMENTO DI MEDICINA  

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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