Search Results - "Galán Carrillo, Isabel"

Double filtration plasmapheresis in the treatment of pancreatitis due to severe hypertriglyceridemia by Galán Carrillo, Isabel, MD, Demelo-Rodriguez, Pablo, MD, Rodríguez Ferrero, María Luisa, MD, Anaya, Fernando, MD, PhD

“…Background Severe hypertriglyceridemia (HTG) leads to major complications such as acute pancreatitis. Lipoprotein apheresis has been proposed as a therapeutic…”
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Impact of Serum Magnesium Levels on Kidney and Cardiovascular Prognosis and Mortality in CKD Patients by Galán Carrillo, Isabel, Vega, Almudena, Goicoechea, Marian, Shabaka, Amir, Gatius, Serena, Abad, Soraya, López-Gómez, Juan Manuel

“…In the general population, hypomagnesemia has been associated with cardiovascular events and hypermagnesemia with overall mortality. In chronic kidney disease…”
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Multidisciplinary management improves the genetic diagnosis of hereditary kidney diseases in the next generation sequencing (NGS) era by Galán Carrillo, Isabel, Galbis Martínez, Liliana, Martínez, Víctor, Roca Meroño, Susana, Ramos, Fernanda, González Rodríguez, Juan David, Piñero Fernández, Juan, Guillén Navarro, Encarnación

“…Hereditary kidney diseases (HKD) are a frequent cause of chronic kidney disease, and their diagnosis has increased since the introduction of next generation…”
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Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases by Martínez Jiménez, Víctor, Ortuño López, Pedro Pablo, Roca Meroño, Susana, Rodríguez Peña, Lidia, Galán Carrillo, Isabel, Galbis Martínez, Liliana, Ramos Carrasco, Fernanda, Piñero Hernández, Juan Alberto, González Rodríguez, Juan David, Guillén Navarro, Encarnación

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El manejo multidisciplinar mejora el diagnóstico genético de las enfermedades renales hereditarias en la era de next generation sequencing (NGS) by Galán Carrillo, Isabel, Galbis Martínez, Liliana, Martínez, Víctor, Roca Meroño, Susana, Ramos, Fernanda, González Rodríguez, Juan David, Piñero Fernández, Juan, Guillén Navarro, Encarnación

“…Resumen: Antecedentes y objetivo: Las enfermedades renales hereditarias (ERH) son una causa frecuente de enfermedad renal crónica, habiéndose incrementado su…”
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Síndrome orofaciodigital tipo i: en el diagnóstico diferencial de la poliquistosis renal autosómica dominante, a próposito de 3 casos by Martínez Jiménez, Víctor, Ortuño López, Pedro Pablo, Roca Meroño, Susana, Rodríguez Peña, Lidia, Galán Carrillo, Isabel, Galbis Martínez, Liliana, Ramos Carrasco, Fernanda, Piñero Hernández, Juan Alberto, González Rodríguez, Juan David, Guillén Navarro, Encarnación

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Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases by Martínez Jiménez, Víctor, Ortuño López, Pedro Pablo, Roca Meroño, Susana, Rodríguez Peña, Lidia, Galán Carrillo, Isabel, Galbis Martínez, Liliana, Ramos Carrasco, Fernanda, Piñero Hernández, Juan Alberto, González Rodríguez, Juan David, Guillén Navarro, Encarnación

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Estudio genético en adultos con glomeruloesclerosis focal y segmentaria by Pilco-Terán, Melissa, Shabaka, Amir, Furlano, Mónica, Tato Ribera, Ana, Galán Carrillo, Isabel, Gutiérrez, Eduardo, Torra, Roser, Fernández-Juárez, Gema

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6359 DAPAGLIFLOZIN TREATMENT IN AUTOSOMAL DOMINANT ALPORT SYNDROME (ADAS) by Carrillo, Isabel Galan, Gatius, Serena, Galvez, Ana Cristina Rodenas

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2068 Factors affecting disease progression in individuals with heterozygous COL4A3/COL4A4 pathogenic variants by Teran, Melissa Pilco, Furlano, Monica, Pybus, Marc, Jiménez, Víctor Martínez, Gomá-Garcés, Elena, Carrillo, Isabel Galan, Leon, Rafael, Romeo, Maria Jose Soler, de Arizón, Leonor Fayos, Perera, Alexandre, Ars, Elisabet, Torra, Roser

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2903 Comprehensive lipidomic analysis reveals further insights into the molecular mechanism of podocyte lipotoxicity in Alport syndrome by Shabaka, Amir, Requena, Belen Fernandez, Gonzalez-Riano, Carolina, Lanzon, Borja, Martinez, Sara, Gradillas, Ana, Carrillo, Isabel Galan, Bosch, Teresa Bada, Sevillano, Angel, Medina-Gomez, Gema, Barbas, Coral, Juarez, Gema Maria Fernandez

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MO039: Multidisciplinary approach improves genetic diagnosis of Alport syndrome in the next-generation sequencing ERA by Galan Carrillo, Isabel, Galbis, Liliana, Martínez Jiménez, Víctor, Pablo Ortuño, Pedro, Roca, Susana, David Castro, Juan, Ramos, Fernanda, Rodríguez, Lidia, Guillén, Encarnación

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5351 IMPACT OF ADD-ON STEROID AND IMMUNOSUPPRESSIVE TREATMENT IN PATIENTS WITH RAPIDLY PROGRESSIVE SECONDARY IGA NEPHROPATHY by Shabaka, Amir, Barceló, Sara Aldana, Sevillano, Angel, Pérez, Javier Vian, Hadad-Arrascue, Fernando, Rodriguez-Moreno, Antolina, Huerta, Ana, Reguera, María José, Lorente, Loreto Fernandez, Carrillo, Isabel Galan, Sierra, Milagros, Juarez, Gema Maria Fernandez

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P0478CLINICOPATHOLOGICAL CHARACTERISTICS AND TREATMENT OUTCOMES OF IGM NEPHROPATHY by Shabaka, Amir, Procaccini, Fabio, Gatius, Serena, Valdes, Elena, Galan Carrillo, Isabel, Cases Corona, Clara Maria, Fernandez Juarez, Gema Maria

“…Abstract Background and Aims IgM nephropathy (IgMN) is a controversial clinicopathological entity that is characterized by the presence of dominant diffuse…”
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MO044TARGETED NEXT GENERATION SEQUENCING AND MULTIDISCIPLINARY APPROACH IN AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE, ALPORT DISEASE AND FAMILIAL HAEMATURIA: GENETIC SPECTRUM AND CLINICAL UTILITY IN A SPANISH COHORT by Galan Carrillo, Isabel, Galbis, Liliana, Martínez Jiménez, Víctor, Castro, Juan David, Ramos, Fernanda, Roca, Susana, Rodríguez, Lidia, Piñero, Juan, Guillén, Encarnación

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