Search Results - "Reynoso, Carolina"

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    Translational Echocardiography: The Dog as a Clinical Research Model of Cardiac Dysfunction by Flores Dueñas, Cesar Augusto, Cordero Yañez, Ignacio Alonso, González, Roberto Mujica, Herrera Ramírez, José Carlomán, Montaño Gómez, Martín Francisco, Gaxiola Camacho, Soila Maribel, García Reynoso, Issa Carolina

    Published in Applied sciences (01-03-2023)
    “…Heart disease is a major contributor to mortality and disability on a global scale. Hence, there is a need for research to improve non-invasive diagnostic…”
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    Journal Article
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    Clinical and pathological factors associated with Ehrlichia canis in companion dogs by Espino-Solís, Gerardo Pavel, Flores-Lira, Erika Astrid, Barreras-Serrano, Alberto, García-Reynoso, Issa Carolina, De la Mora Covarrubias, Antonio, Jiménez Vega, Florinda, Escárcega-Ávila, Angélica

    “…Canine monocytic ehrlichiosis (CME) is a disease caused by the Gram-negative bacteria Ehrlichia canis, a bacterium that affects domestic dogs but can also…”
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    Journal Article
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    Consenso de hemofilia en México by López-Arroyo, José L., Pérez-Zúñiga, Juan M., Merino-Pasaye, Laura E., Saavedra-González, Azucena, Alcivar-Cedeño, Luisa M., Álvarez-Vera, José Luis, Anaya-Cuellar, Irene, Arana-Luna, Luara L., Ávila-Castro, David, Bates-Martín, Ramón A., Cesarman-Maus, Gabriela, Chávez-Aguilar, Lénica A., de la Peña-Celaya, José A., Espitia-Ríos, María E., Estrada-Domínguez, Patricia, Fermín-Caminero, Denisse J., Flores-Patricio, Willy, García-Chávez, Jaime, García-Lee, María T., González-Pérez, Ma. del Carmen, González-Rubio, María del C., González-Villareal, Ma. Guadalupe, Ramírez-Moreno, Fabiola, Hernández-Colin, Ana K., Hernández-Ruiz, Eleazar, Herrera-Olivares, Wilfrido, Leyto-Cruz, Faustino, Loera-Fragoso, Sergio J., Orellana-Garibay, Juan J., Palma-Moreno, Orlando G., Paredes-Lozano, Eugenia P., Peña-Alcántara, Paula, Pérez-Lozano, Uendy, Pichardo-Cepín, Yayra M., Carolina-Reynoso, Ana, Rodríguez-Serna, Mishel, Rojas-Castillejos, Flavio, Romero-Rodelo, Hilda, Ruíz-Contreras, Josué I., Segura-García, Adela, Silva-Vera, Karina, Soto-Cisneros, Paulina M., Tapia-Enríquez, Ana L., Tavera-Rodríguez, Martha G., Teomitzi-Sánchez, Óscar, Tepepa-Flores, Fredy, Valencia-Rivas, María D., Valle-Cárdenas, Teresa, Varela-Constantino, Ana, Javier-Morales, Adrián, Martínez-Ramírez, Mario A., Tena-Cano, Sergio, Terrazas-Marín, Ricardo, Vilchis-González, Shendel P., Villela-Peña, Atenas, Mena-Zepeda, Verónica, Alvarado-Ibarra, Martha

    Published in Gaceta médica de México (28-03-2023)
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    Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity by Espinoza, Ivan O, Reynoso, Carolina, Chávez, Giulliana, Engel, Andrew G

    Published in Medwave (04-06-2019)
    “…The congenital myasthenic syndromes are a heterogeneous group of genetic disorders characterized by an abnormal synaptic transmission in the neuromuscular…”
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    Journal Article
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    IS DIABETIC KETOACIDOSIS MANAGEMENT SAFE AND SUCCESFUL IN INTERNAL MEDICINE? ASSESSMENT OF 90 EPISODES HANDLED UNDER PROTOCOL by Carolina Reynoso, Guillermo Marcucci, Luz Carolina Dromi, Hugo Lavandaio, José Alberto Carena

    “…Introduction: diabetic ketoacidosis (DKA) is an acute and serious complication that compromises the life of the patient with diabetes mellitus (DM). Their…”
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    Journal Article
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    Es exitoso y seguro el manejo en clínica médica de la Cetoacidosis diabética? Evaluación de 90 episodios manejados protocolizadamente by Reynoso, Carolina, Marcucci, Guillermo, Dromi, Luz Carolina, Lavandaio, Hugo, Carena, José Alberto

    “…Introducción: la cetoacidosis diabética (CAD) es una complicación aguda y grave que compromete la vida del paciente con diabetes mellitus (DM). Su mortalidad…”
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    Journal Article
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    Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity by Ivan O. Espinoza, Carolina Reynoso, Giulliana Chávez, Andrew G Engel

    Published in Medwave (01-06-2019)
    “…Introducción Los síndromes miasténicos congénitos son un grupo heterogéneo de desórdenes genéticos, caracterizados por una transmisión sináptica anormal en la…”
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    Journal Article
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    Consensus on hemophilia in Mexico by López-Arroyo, José L., Pérez-Zúñiga, Juan M., Merino-Pasaye, Laura E., Saavedra-González, Azucena, Alcivar-Cedeño, Luisa M., Álvarez-Vera, José Luis, Anaya-Cuellar, Irene, Arana-Luna, Luara L., Ávila-Castro, David, Bates-Martín, Ramón A., Cesarman-Maus, Gabriela, Chávez-Aguilar, Lénica A., de la Peña-Celaya, José A., Espitia-Ríos, María E., Estrada-Domínguez, Patricia, Fermín-Caminero, Denisse J., Flores-Patricio, Willy, García-Chávez, Jaime, García-Lee, María T., González-Pérez, Ma. del Carmen, González-Rubio, María del C., González-Villareal, Ma. Guadalupe, Ramírez-Moreno, Fabiola, Hernández-Colin, Ana K., Hernández-Ruiz, Eleazar, Herrera-Olivares, Wilfrido, Leyto-Cruz, Faustino, Loera-Fragoso, Sergio J., Orellana-Garibay, Juan J., Palma-Moreno, Orlando G., Paredes-Lozano, Eugenia P., Peña-Alcántara, Paula, Pérez-Lozano, Uendy, Pichardo-Cepín, Yayra M., Carolina-Reynoso, Ana, Rodríguez-Serna, Mishel, Rojas-Castillejos, Flavio, Romero-Rodelo, Hilda, Ruíz-Contreras, Josué I., Segura-García, Adela, Silva-Vera, Karina, Soto-Cisneros, Paulina M., Tapia-Enríquez, Ana L., Tavera-Rodríguez, Martha G., Teomitzi-Sánchez, Óscar, Tepepa-Flores, Fredy, Valencia-Rivas, María D., Valle-Cárdenas, Teresa, Varela-Constantino, Ana, Javier-Morales, Adrián, Martínez-Ramírez, Mario A., Tena-Cano, Sergio, Terrazas-Marín, Ricardo, Vilchis-González, Shendel P., Villela-Peña, Atenas, Mena-Zepeda, Verónica, Alvarado-Ibarra, Martha

    Published in Gaceta médica de México (31-03-2023)
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    Journal Article
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    Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosity by Espinoza, Ivan O, Reynoso, Carolina, Chávez, Giulliana, Engel, Andrew G

    Published in Medwave (04-06-2019)
    “…INTRODUCTIONThe congenital myasthenic syndromes are a heterogeneous group of genetic disorders characterized by an abnormal synaptic transmission in the…”
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