Partial replacement of fat and salt in liver pâté by addition of Agaricus bisporus and Pleurotus ostreatus flour von Cerón‐Guevara, Magdalena I., Santos, Eva M., Lorenzo, José M., Pateiro, Mirian, Bermúdez‐Piedra, Roberto, Rodríguez, José A., Castro‐Rosas, Javier, Rangel‐Vargas, Esmeralda

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Effect of the addition of edible mushroom flours (Agaricus bisporus and Pleurotus ostreatus) on physicochemical and sensory properties of cold‐stored beef patties von Cerón‐Guevara, Magdalena I., Rangel‐Vargas, Esmeralda, Lorenzo, José Manuel, Bermúdez, Roberto, Pateiro, Mirian, Rodriguez, José A., Sanchez-Ortega, Irais, Santos, Eva M.

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Classic infantile‐onset Pompe disease with histopathological neurologic findings linked to a novel GAA gene 4 bp deletion: A case study von Cerón‐Rodríguez, Magdalena, Castillo‐García, Daniela, Acosta‐Rodríguez‐Bueno, Carlos‐Patricio, Aguirre‐Hernández, Jesús, Murillo‐Eliosa, Juan‐Rafael, Valencia‐Mayoral, Pedro, Escobar‐Sánchez, Argelia, Salgado‐Loza, Juan‐Luis

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Description of the initial approach to patients with suspected child abuse in the emergency department of a pediatric hospital von Guerrero-Reséndiz, Diana A., Gómez Chavarría, María T., Olivar-López, Víctor, Cerón-Rodríguez, Magdalena, Villa-Guillén, Mónica, Márquez-González, Horacio

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c.1898C>G/p.Ser633Trp Mutation in Alpha-l-Iduronidase: Clinical and Structural Implications von Peña-Gomar, Iliana, Jiménez-Mariscal, José L., Cerón, Magdalena, Rosas-Trigueros, Jorge, Reyes-López, Cesar A.

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Renal globotriaosylceramide deposits for Fabry disease linked to uncertain pathogenicity gene variant c.352C>T/p.Arg118Cys: A family study von Cerón‐Rodríguez, Magdalena, Ramón‐García, Guillermo, Barajas‐Colón, Edgar, Franco‐Álvarez, Isidro, Salgado‐Loza, Juan L.

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Improvement of life quality measured by Lansky Score after enzymatic replacement therapy in children with Gaucher disease type 1 von Cerón‐Rodríguez, Magdalena, Barajas‐Colón, Edgar, Ramírez‐Devars, Lyuva, Gutiérrez‐Camacho, Claudia, Salgado‐Loza, Juan L.

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Adhesion to the enzymatic replacement therapy in Gaucher disease and the effect on the bone health von Cerón, Magdalena

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Reduction of Salt and Fat in Frankfurter Sausages by Addition of Agaricus bisporus and Pleurotus ostreatus Flour von Cerón-Guevara, Magdalena I., Rangel-Vargas, Esmeralda, Lorenzo, José M., Bermúdez, Roberto, Pateiro, Mirian, Rodríguez, Jose A., Sánchez-Ortega, Irais, Santos, Eva M.

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Consenso de expertos sobre recomendaciones basadas en evidencia para el diagnóstico, tratamiento y seguimiento de enfermedad de Fabry en pediatría von Baquero Rodríguez, Richard, Trimarchi, Hernán, Martínez Cáceres, Lyda Esperanza, Valencia, Maylin, Liern, Miguel, Cárdenas Aguilera, Juan Guillermo, Gutiérrez Sepúlveda, María Paula, Estévez Capacho, Mayra Alexandra, Carrascal Guzmán, Martha, Cerón Rodríguez, Magdalena, Ospina-Lagos, Sandra Yaneth, Rodríguez, Edisson, Mateus Arbeláez, Heidi, Chacon, Kelly Rocio, Fainboin, Alejandro, Reina Ávila, María Fernanda, Serrano Gayubo, Ana K, Germain, Dominique P, Cabrera, Gustavo, Prieto, Juan Carlos, Politei, Juan Manuel, Rodríguez Cuéllar, Carmen Inés

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Upgrading the evidence for the use of ambroxol in Gaucher disease and GBA related Parkinson: Investigator initiated registry based on real life data von Istaiti, Majdolen, Revel‐Vilk, Shoshana, Becker‐Cohen, Michal, Dinur, Tama, Ramaswami, Uma, Castillo‐Garcia, Daniela, Ceron‐Rodriguez, Magdalena, Chan, Alicia, Rodic, Predrag, Tincheva, Radka Stefanova, Al‐Hertani, Walla, Lee, Beom Hee, Yang, Chia‐Feng, Kiec‐Wilk, Beata, Fiumara, Agata, Rubio, Barbara, Zimran, Ari

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Genotype/phenotype correlation from mucopolysaccharidosis type I: Hurler, Hurler-Scheie, and Scheie syndromes and the response to enzymatic replacement therapy von Cerón-Rodriguez, Magdalena

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Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population von Cerón-Rodríguez, Magdalena, Vázquez-Martínez, Edgar Ricardo, García-Delgado, Constanza, Ortega-Vázquez, Alberto, Valencia-Mayoral, Pedro, Ramírez-Devars, Lyuva, Arias-Villegas, Christian, Monroy-Muñoz, Irma Eloísa, López, Marisol, Cervantes, Alicia, Cerbón, Marco, Morán-Barroso, Verónica Fabiola

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c.1898CG/p.Ser633Trp Mutation in Alpha-l-Iduronidase: Clinical and Structural Implications von Peña-Gomar, Iliana, Jiménez-Mariscal, José L, Cerón, Magdalena, Rosas-Trigueros, Jorge, Reyes-López, Cesar A

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Are genotype and biomarkers enough to initiate enzyme replacement therapy in Fabry disease? The value of the biopsy von Cerón-Rodriguez, Magdalena, Castillo-García, Daniela

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Pediatric Fabry disease in Mexico: Genotype-phenotype relationship von Cerón-Rodriguez, Magdalena, Cifuentes-Uribe, Karla, Vargas, Cinthia D., Acosta Rodríguez Bueno, Carlos P.

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First experience with olipudase alfa for ASMD type B in Mexico von Sanchez, Luz Maria, Rodriguez, Magdalena Ceron

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The impact of vitamin D in patients with lysosomal diseases on ERT von Acosta Rodríguez Bueno, Carlos P., Cerón-Rodriguez, Magdalena, De la Cruz Carmen, Marlen, Ortega, Israel Parra

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P418: The diagnostic journey of Mexican patients with Verheij syndrome von Cifuentes-Uribe, Karla, Reyes-De La Rosa, Alejandra, Moreno-Salgado, Rodrigo, Villasenor-Dominguez, America, Ceron-Rodriguez, Magdalena, Viveros-Rodriguez, Romina, Cortes-Gonzalez, Vianney, Garza-Mayén, Gilda

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Mucopolysaccharidosis type II (Hunter syndrome) with multisystem Langerhans cell histiocytosis - A case report of a not described association von Castillo-García, Daniela, Cerón-Rodríguez, Magdalena, Amici-García, Alba Valentina

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