Progression of myocardial fibrosis by magnetic resonance imaging in patients with Duchenne and Becker muscular dystrophy von Silva, Marly C, Meira, Zilda M, Giannetti, Juliana G, Lara, Marco A, Vainzof, Mariz, Zatz, Mayana, Kalil-Filho, Roberto, Rochitte, Carlos E

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Approach to the diagnosis of congenital myopathies von North, Kathryn N, Wang, Ching H, Clarke, Nigel, Jungbluth, Heinz, Vainzof, Mariz, Dowling, James J, Amburgey, Kimberly, Quijano-Roy, Susana, Beggs, Alan H, Sewry, Caroline, Laing, Nigel G, Bönnemann, Carsten G

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Association between specific dystrophin gene mutations and myocardial fibrosis by cardiovascular magnetic resonance imaging in patients with Duchenne and Becker muscular dystrophy von Silva, Marly C, Rassi, Carlos H, Meira, Zilda M, Giannetti, Juliana G, Vainzof, Mariz, Zatz, Mayana, Kalil, Roberto, Rochitte, Carlos E

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Progression of myocardial fibrosis by magnetic resonance imaging in patients with Duchenne and Becker muscular dystrophy and preserved left ventricular ejection fraction - a random... von Silva, Marly C, Rassi, Carlos H, Meira, Zilda M, Giannetti, Juliana G, Vainzof, Mariz, Zatz, Mayana, Kalil, Roberto, Rochitte, Carlos E

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Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes von Vianna, Gabrielle S., Freitas, Mariana L., de Oliveira, Valdirene T., Pietra, Rafaella X., da S. Gonçalves, Michele, Rocha, Patrícia P.O., Monteiro, Rejane A.C., Ferreira, Luana C.A., Xavier, Rosana R., Carvalho, Andréia M., de M. Lima, Patrícia R., Monteiro, Maria Augusta N.P., Mateo, Elvis C., Giannetti, Juliana G., da C. César, Giovana, de S. Lima, Joziele, Medeiros, Paula F.V., Jehee, Fernanda S.

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A novel complex neurological phenotype due to a homozygous mutation in FDX2 von Gurgel-Giannetti, Juliana, Lynch, David S, Paiva, Anderson Rodrigues Brandão de, Lucato, Leandro Tavares, Yamamoto, Guilherme, Thomsen, Christer, Basu, Somsuvro, Freua, Fernando, Giannetti, Alexandre Varella, de Assis, Bruno Della Ripa, Ribeiro, Mara Dell Ospedale, Barcelos, Isabella, Sayão Souza, Katiane, Monti, Fernanda, Melo, Uirá Souto, Amorim, Simone, Silva, Leonardo G L, Macedo-Souza, Lúcia Inês, Vianna-Morgante, Angela M, Hirano, Michio, Van der Knaap, Marjo S, Lill, Roland, Vainzof, Mariz, Oldfors, Anders, Houlden, Henry, Kok, Fernando

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Preparation of Fluorescent Carbon-Based Dots from Waste Tire Pyrolysis von Parra, Juliana B., Silva, Karina C., Valezin, Pedro A. S., Martins, Raphael G., Gomes, Rodolfo R., Pereira, Rafael S., de Melo, Fernando M., Morandim-Giannetti, Andreia de A., dos Santos, Ronaldo G., Panzarini, Luz Consuelo G. A., Toyama, Marcos M.

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Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization von Gurgel-Giannetti, Juliana, Souza, Lucas Santos, Yamamoto, Guilherme L, Belisario, Marina, Lazar, Monize, Campos, Wilson, Pavanello, Rita de Cassia M, Zatz, Mayana, Reed, Umbertina, Zanoteli, Edmar, Oliveira, Acary Bulle, Lehtokari, Vilma-Lotta, Casella, Erasmo B, Machado-Costa, Marcela C, Wallgren-Pettersson, Carina, Laing, Nigel G, Nigro, Vincenzo, Vainzof, Mariz

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Consensus Statement on Standard of Care for Congenital Myopathies von Wang, Ching H., Dowling, James J., North, Kathryn, Schroth, Mary K., Sejersen, Thomas, Shapiro, Frederic, Bellini, Jonathan, Weiss, Hali, Guillet, Marc, Amburgey, Kimberly, Apkon, Susan, Bertini, Enrico, Bonnemann, Carsten, Clarke, Nigel, Connolly, Anne M., Estournet-Mathiaud, Brigitte, Fitzgerald, Dominic, Florence, Julaine M., Gee, Richard, Gurgel-Giannetti, Juliana, Glanzman, Allan M., Hofmeister, Brittany, Jungbluth, Heinz, Koumbourlis, Anastassios C., Laing, Nigel G., Main, Marion, Morrison, Leslie A., Munns, Craig, Rose, Kristy, Schuler, Pamela M., Sewry, Caroline, Storhaug, Kari, Vainzof, Mariz, Yuan, Nanci

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Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement von Hotchkiss, Leslie, Donkervoort, Sandra, Leach, Meganne E., Mohassel, Payam, Bharucha-Goebel, Diana X., Bradley, Nathaniel, Nguyen, David, Hu, Ying, Gurgel-Giannetti, Juliana, Bönnemann, Carsten G.

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International retrospective natural history study of LMNA-related congenital muscular dystrophy von Ben Yaou, Rabah, Yun, Pomi, Dabaj, Ivana, Norato, Gina, Donkervoort, Sandra, Xiong, Hui, Nascimento, Andrés, Maggi, Lorenzo, Sarkozy, Anna, Monges, Soledad, Bertoli, Marta, Komaki, Hirofumi, Mayer, Michèle, Mercuri, Eugenio, Zanoteli, Edmar, Castiglioni, Claudia, Marini-Bettolo, Chiara, D’Amico, Adele, Deconinck, Nicolas, Desguerre, Isabelle, Erazo-Torricelli, Ricardo, Gurgel-Giannetti, Juliana, Ishiyama, Akihiko, Kleinsteuber, Karin S, Lagrue, Emmanuelle, Laugel, Vincent, Mercier, Sandra, Messina, Sonia, Politano, Luisa, Ryan, Monique M, Sabouraud, Pascal, Schara, Ulrike, Siciliano, Gabriele, Vercelli, Liliana, Voit, Thomas, Yoon, Grace, Alvarez, Rachel, Muntoni, Francesco, Pierson, Tyler M, Gómez-Andrés, David, Reghan Foley, A, Quijano-Roy, Susana, Bönnemann, Carsten G, Bonne, Gisèle

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Motor assessment in patients with Duchenne muscular dystrophy von Diniz, Gabriela Palhares Campolina, Lasmar, Laura Maria de Lima Belizário Facury, Giannetti, Juliana Gurgel

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Preparation of Fluorescent Carbon-Based Dots from Waste Tire Pyrolysis von Parra, Juliana B., Silva, Karina C., Valezin, Pedro A. S., Martins, Raphael G., Gomes, Rodolfo R., Pereira, Rafael S., Melo, Fernando M. De, Morandim-Giannetti, Andreia De A., Santos, Ronaldo G. Dos, Panzarini, Luz Consuelo G. A., Toyama, Marcos M.

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