SYREN, EVA MARIE LOUISE
SYREN, EVA MARIE LOUISE
Dipartimento di Scienze Cliniche e di Comunità
ABCB4 mutations in adult patients with cholestatic liver disease : impact and phenotypic expression
2016 D. Degiorgio, A. Crosignani, C. Colombo, D. Bordo, M. Zuin, E. Vassallo, M. Syrén, D.A. Coviello, P.M. Battezzati
Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome
2006 G. Vezzoli, T. Arcidiacono, V. Paloschi, A. Terranegra, M.R. Biasion, G. Weber, S. Mora, M.L. Syren, D. Coviello, D. Cusi, G. Bianchi, L. Soldati
Bioactive Compounds in Edible Oils and Their Role in Oxidative Stress and Inflammation
2021 A. Mazzocchi, V. De Cosmi, P. Risé, G.P. Milani, S. Turolo, M. Syrén, A. Sala, C. Agostoni
Comparative Analysis of Docosahexaenoic Acid (DHA) Content in Mother's Milk of Term and Preterm Mothers
2022 G. Vizzari, D. Morniroli, F. Alessandretti, V. Galli, L. Colombo, S. Turolo, M. Syren, N. Pesenti, C. Agostoni, F. Mosca, M.L. Gianni
Ereditabilita’ della massa minerale ossea: studio nei gemelli monozigoti e dizigoti
2002 G. Vezzoli, C. Bianchin, T. Arcidiacono, D. Adamo, A. Terranegra, D. Coviello, M.L. Syren, A. Rubinacci, L. Soldati
Genetic analysis of Bartter and Gitelman syndrome in the Italian population
2005 N. Borsa, M.-. Syrén, C. Mattiello, D.A. Coviello, M. Travi, A. Bettinelli, S. Tedeschi
Il polimorfismo Arg990Gly del gene del Ca sensing receptor causa un guadagno funzionale e predispone all'ipercalciria primaria
2005 T. Arcidiacono, V. Paloschi, A. Terranegra, R. Biasion, M.L. Syren, G. Coviello, D. Cusi, A. Rubinacci, L. Soldati, G. Vezzoli
Il test dell'idroclorotiazide nella malattia di Gitelman: una valida alternativa alla biologia molecolare
2005 A. Bettinelli, G. Colussi, M.G. Bianchetti, M.-. Syrén, N. Borsa, C. Mattiello, A. Edefonti, P. Brambilla, S. Tedeschi
Le sindromi di Bartter-Gitelman. Risultati di uno studio clinico e di biologia molecolare condotto su 101 pazienti
2005 A. Bettinelli, S. Tedeschi, D. Coviello, N. Borsa, C. Mattiello, M.-. Syrén, A. Edefonti, M.G. Bianchetti
Long-Chain Polyunsaturated Fatty Acids Supplementation and Respiratory Infections
2022 V. De Cosmi, A. Mazzocchi, S. Turolo, M.L. Syren, G.P. Milani, C. Agostoni
N-3 polyunsatured fatty acids in menopausal transition: A systematic review of depressive and cognitive disorders with accompanying vasomotor symptoms
2018 V. Ciappolino, A. Mazzocchi, P. Enrico, M. Syrén, G. Delvecchio, C. Agostoni, P. Brambilla
Persistent Abnormalities of Fatty Acids Profile in Children With Idiopathic Nephrotic Syndrome in Stable Remission
2021 S. Turolo, A.C. Edefonti, W. Morello, M.-. Syren, V. De Cosmi, L. Ghio, C. Tamburello, E.A. Demarco, A. Berrettini, G. Manzoni, C. Agostoni, G. Montini
R990G polymorphism of calcium-sensing receptor does produce a gain-of-function and predispose to primary hypercalciuria
2007 G. Vezzoli, A. Terranegra, T. Arcidiacono, M.R. Biasion, D. Coviello, E.M.L. Syren, V. Paloschi, S. Giannini, G. Mignogna, A. Rubinacci, A. Ferraretto, D.M. Cusi, G. Bianchi, L. Soldati
R990G polymorphism of the calcium-sensing receptor and renal calcium excretion in patients with primary hyperparathyroidism
2006 S. Corbetta, C. Eller-Vainicher, M. Filopanti, P. Saeli, G. Vezzoli, T. Arcidiacono, P. Loli, M.L. Syren, L. Soldati, P. Beck-Peccoz, A. Spada
Renal phosphate handling in Gitelman syndrome : the results of a case–control study
2013 C. Viganò, C. Amoruso, F. Barretta, G. Minnici, W. Albisetti, E. Syren, M.G. Bianchetti, A. Bettinelli
Simultaneous mutations in the CLCNKB and SLC12A3 genes in two siblings with phenotypic heterogeneity in classic Bartter syndrome
2005 A. Bettinelli, N. Borsa, E.M.L. Syren, C. Mattiello, D. Coviello, A. Edefonti, M. Giani, M. Travi, S. Tedeschi
The polyunsaturated fatty acid balance in kidney health and disease : A review
2018 M. Syren, S. Turolo, F. Marangoni, G.P. Milani, A. Edefonti, G. Montini, C. Agostoni