Identification and functional characterization of five novel mutant alleles in 58 Italian patients with Gaucher disease type 1 by Miočić, Snježana, Filocamo, Mirella, Dominissini, Silvia, Montalvo, Anna Lisa E., Vlahoviček, Kristian, Deganuto, Marta, Mazzotti, Raffaella, Cariati, Roberta, Bembi, Bruno, Pittis, Maria Gabriela

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MLP (muscle LIM protein) as a stress sensor in the heart by Buyandelger, Byambajav, Ng, Keat-Eng, Miocic, Snjezana, Piotrowska, Izabela, Gunkel, Sylvia, Ku, Ching-Hsin, Knöll, Ralph

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α-myosin heavy chain : A sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy by CARNIEL, Elisa, TAYLOR, Matthew R. G, GRAW, Sharon L, FEIGER, Jennie, XIAO ZHONG ZHU, DAO, Dmi, FERGUSON, Debra A, BRISTOW, Michael R, MESTRONI, Luisa, SINAGRA, Gianfranco, DI LENARDA, Andrea, KU, Lisa, FAIN, Pamela R, BOUCEK, Mark M, CAVANAUGH, Mi Jean, MIOCIC, Snjezana, SLAVOV, Dobromir

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A Common MLP (Muscle LIM Protein) Variant Is Associated With Cardiomyopathy by Knöll, Ralph, Kostin, Sawa, Klede, Stefanie, Savvatis, Kostas, Klinge, Lars, Stehle, Ina, Gunkel, Sylvia, Kötter, Sebastian, Babicz, Kamila, Sohns, Melanie, Miocic, Snjezana, Didié, Michael, Knöll, Gudrun, Zimmermann, Wolfram Hubertus, Thelen, Paul, Bickeböller, Heike, Maier, Lars S, Schaper, Wolfgang, Schaper, Jutta, Kraft, Theresia, Tschöpe, Carsten, Linke, Wolfgang A, Chien, Kenneth R

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Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement by BRODSKY, G. L, MUNTONI, F, MIOCIC, S, SINAGRA, G, SEWRY, C, MESTRONI, L

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Telethonin Deficiency Is Associated With Maladaptation to Biomechanical Stress in the Mammalian Heart by Knöll, Ralph, Linke, Wolfgang A, Zou, Peijian, Miočiċ, Snježana, Kostin, Sawa, Buyandelger, Byambajav, Ku, Ching-Hsin, Neef, Stefan, Bug, Monika, Schäfer, Katrin, Knöll, Gudrun, Felkin, Leanne E, Wessels, Johannes, Toischer, Karl, Hagn, Franz, Kessler, Horst, Didié, Michael, Quentin, Thomas, Maier, Lars S, Teucher, Nils, Unsöld, Bernhard, Schmidt, Albrecht, Birks, Emma J, Gunkel, Sylvia, Lang, Patrick, Granzier, Henk, Zimmermann, Wolfram-Hubertus, Field, Loren J, Faulkner, Georgine, Dobbelstein, Matthias, Barton, Paul J.R, Sattler, Michael, Wilmanns, Matthias, Chien, Kenneth R

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Familial dilated cardiomyopathy : Evidence for genetic and phenotypic heterogeneity by MESTRONI, L, ROCCO, C, MCKENNA, W. J, FALASCHI, A, GIACCA, M, CAMERINI, F, GREGORI, D, SINAGRA, G, DI LENARDA, A, MIOCIC, S, VATTA, M, PINAMONTI, B, MUNTONI, F, CAFORIO, A. L. P

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Genetics of Mechanosensation in the Heart by Buyandelger, Byambajav, Ng, Keat-Eng, Miocic, Snjezana, Gunkel, Sylvia, Piotrowska, Izabela, Ku, Ching-Hsin, Knöll, Ralph

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Identification of four novel mutations in the alpha glucosidase gene in five Italian patients with infantile onset glycogen storage disease type II by Pittis, Maria Gabriela, Montalvo, Anna Lisa E., Miocic, Snjezana, Martini, Cristina, Deganuto, Marta, Candusso, Manila, Ciana, Giovanni, Bembi, Bruno

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Familial dilated cardiomyopathy by Mestroni, Luisa, Rocco, Chiara, Gregori, Dario, Sinagra, Gianfranco, Di Lenarda, Andrea, Miocic, Snjezana, Vatta, Matteo, Pinamonti, Bruno, Muntoni, Francesco, Caforio, Alida L.P., McKenna, William J., Falaschi, Arturo, Giacca, Mauro, Camerini, Fulvio

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Familial dilated cardiomyopathy: Evidence for genetic and phenotypic heterogeneity by Mestroni, Luisa, Rocco, Chiara, Gregori, Dario, Sinagra, Gianfranco, Di Lenarda, Andrea, Miocic, Snjezana, Vatta, Matteo, Pinamonti, Bruno, Muntoni, Francesco, Caforio, Alida L.P., McKenna, William J., Falaschi, Arturo, Giacca, Mauro, Camerini, Fulvio

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