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Search Results - Ramirez-Fernandez, Alicia
Search Results - Ramirez-Fernandez, Alicia
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Cardioprotection with halogenated gases: how does it occur?
by
Guerrero-Orriach, Jose Luis
,
Escalona Belmonte, Juan Jose
,
Ramirez Fernandez, Alicia
,
Ramirez Aliaga, Marta
,
Rubio Navarro, Manuel
,
Cruz Mañas, Jose
Published in
Drug design, development and therapy
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Renal and Neurologic Benefit of Levosimendan vs Dobutamine in Patients With Low Cardiac Output Syndrome After Cardiac Surgery: Clinical Trial FIM-BGC-2014-01
by
Guerrero-Orriach, Jose L
,
Malo-Manso, Alfredo
,
Ramirez-Aliaga, Marta
,
Florez Vela, Ana Isabel
,
Galán-Ortega, Manuel
,
Moreno-Cortes, Isabel
,
Gonzalez-Almendros, Inmaculada
,
Ramirez-Fernandez, Alicia
,
Ariza-Villanueva, Daniel
,
Escalona-Belmonte, Juan Jose
,
Quesada-Muñoz, Guillermo
,
Sepúlveda-Haro, Enrique
,
Romero-Molina, Salvador
,
Bellido-Estevez, Inmaculada
,
Gomez-Luque, Aurelio
,
Rubio-Navarro, Manuel
,
Alcaide-Torres, Juan
,
Santiago-Fernandez, Concepcion
,
Garrido-Sanchez, Lourdes
,
Cruz-Mañas, Jose
Published in
Frontiers in pharmacology
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Cardiac, renal, and neurological benefits of preoperative levosimendan administration in patients with right ventricular dysfunction and pulmonary hypertension undergoing cardiac s...
by
Guerrero-Orriach, José Luis
,
Ariza-Villanueva, Daniel
,
Florez-Vela, Ana
,
Garrido-Sánchez, Lourdes
,
Moreno-Cortés, María Isabel
,
Galán-Ortega, Manuel
,
Ramírez-Fernández, Alicia
,
Alcaide Torres, Juan
,
Fernandez, Concepción Santiago
,
Navarro Arce, Isabel
,
Melero-Tejedor, José María
,
Rubio-Navarro, Manuel
,
Cruz-Mañas, José
Published in
Therapeutics and clinical risk management
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19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype
by
Venegas-Vega, Carlos
,
Nieto-Martínez, Karem
,
Martínez-Herrera, Alejandro
,
Gómez-Laguna, Laura
,
Berumen, Jaime
,
Cervantes, Alicia
,
Kofman, Susana
,
Fernández-Ramírez, Fernando
Published in
Molecular cytogenetics
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Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event
by
Morán‐Barroso, Verónica Fabiola
,
Cervantes, Alicia
,
Rivera‐Vega, María del Refugio
,
del Castillo‐Moreno, Adriana
,
Moreno‐Chacón, Alejandra
,
Mejía‐Cauich, Estefanía
,
Contreras‐Ortiz, Laura Eréndira
,
Fernández‐Ramírez, Fernando
Published in
Molecular genetics & genomic medicine
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Congenital hypertrichosis universalis in Mexican female twins
by
Cervantes, Alicia
,
García‐Delgado, Constanza
,
Fernández‐Ramírez, Fernando
,
Valencia‐Herrera, Adriana
,
Kofman, Susana
,
Morán‐Barroso, Verónica
Published in
International journal of dermatology
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Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature
by
Gómez-Laguna, Laura
,
Martínez-Herrera, Alejandro
,
Reyes-de la Rosa, Alejandra Del Pilar
,
García-Delgado, Constanza
,
Nieto-Martínez, Karem
,
Fernández-Ramírez, Fernando
,
Valderrama-Atayupanqui, Tania Yanet
,
Morales-Jiménez, Ariadna Berenice
,
Villa-Morales, Judith
,
Kofman, Susana
,
Cervantes, Alicia
,
Morán-Barroso, Verónica Fabiola
Published in
Ophthalmic genetics
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Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
by
Cervantes, Alicia
,
García-Delgado, Constanza
,
Fernández-Ramírez, Fernando
,
Galaz-Montoya, Carolina
,
Morales-Jiménez, Ariadna Berenice
,
Nieto-Martínez, Karem
,
Gómez-Laguna, Laura
,
Villa-Morales, Judith
,
Quintana-Palma, Mónica
,
Berúmen, Jaime
,
Kofman, Susana
,
Morán-Barroso, Verónica F
Published in
BMC medical genomics
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19q13.11 microdeletion concomitant with insdn in a boy: potential role of UBA2 in the associated phenotype
by
Venegas-Vega, Carlos
,
Nieto-Martínez, Karem
,
Martínez-Herrera, Alejandro
,
Gómez-Laguna, Laura
,
Berumen, Jaime
,
Cervantes, Alicia
,
Kofman, Susana
,
Fernández-Ramírez, Fernando
Published in
Molecular cytogenetics
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Congenital hypertrichosis universalis in Mexican female twins
by
Cervantes, Alicia
,
García-Delgado, Constanza
,
Fernández-Ramírez, Fernando
,
Valencia-Herrera, Adriana
,
Kofman, Susana
,
Morán-Barroso, Verónica
Published in
International Journal of Dermatology
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Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature
by
Gómez-Laguna, Laura
,
Martínez-Herrera, Alejandro
,
Reyes-de la Rosa, Alejandra del Pilar
,
García-Delgado, Constanza
,
Nieto-Martínez, Karem
,
Fernández-Ramírez, Fernando
,
Valderrama-Atayupanqui, Tania Yanet
,
Morales-Jiménez, Ariadna Berenice
,
Villa-Morales, Judith
,
Kofman, Susana
,
Cervantes, Alicia
,
Morán-Barroso, Verónica Fabiola
Published in
Ophthalmic Genetics
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19q13.11 microdeletion concomitant with ins(2;19)(p25.3;q13.1q13.4)dn in a boy: potential role of UBA2 in the associated phenotype
by
Venegas-Vega, Carlos
,
Nieto-Martínez, Karem
,
Martínez-Herrera, Alejandro
,
Gómez-Laguna, Laura
,
Berumen, Jaime
,
Cervantes, Alicia
,
Kofman, Susana
,
Fernández-Ramírez, Fernando
Published in
Molecular cytogenetics
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