Search Results - "García Cruz, Loida María"

Hiperinsulinismo congénito en Gran Canaria by Nóvoa Medina, Yeray, Domínguez García, Ángela, Quinteiro González, Sofía, García Cruz, Loida María, Santana Rodríguez, Alfredo

“…El hiperinsulinismo congénito (HC) es una patología seria caracterizada por la aparición de hipoglucemias graves. Las mutaciones patogénicas en los genes ABCC8…”
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Congenital hyperinsulinism in Gran Canaria, Canary Isles by Nóvoa-Medina, Yeray, Domínguez García, Angela, Quinteiro González, Sofía, García Cruz, Loida María, Santana Rodríguez, Alfredo

“…Congenital hyperinsulinism (CH) is a severe disorder characterised by the appearance of severe hypoglycaemia. Pathogenic mutations in the ABCC8 and KCNJ11…”
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Adherence to Mediterranean diet is not associated with birthweight - Results form a sample of Canarian pregnant women by Tomaino, Laura, Reyes Suárez, Desiderio, Reyes Domínguez, Ana, García Cruz, Loida María, Ramos Díaz, Marta, Serra Majem, Lluis

“…Background: the prevalence of overweight and obesity showed and increasing trend over the past few years. The burden of this epidemic represents a public…”
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Factors Associated with Stunting among Children Aged 0 to 59 Months from the Central Region of Mozambique by Cruz, Loida M García, Azpeitia, Gloria González, Súarez, Desiderio Reyes, Rodríguez, Alfredo Santana, Ferrer, Juan Francisco Loro, Serra-Majem, Lluis

“…The objective of this study was to identify the major socio-demographic, health, and environmental determinants of stunting among children aged 0-59 months…”
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Congenital hyperinsulinism in Gran Canaria, Canary Isles by Yeray Nóvoa-Medina, Angela Domínguez García, Sofía Quinteiro González, Loida María García Cruz, Alfredo Santana Rodríguez

“…Introduction: Congenital hyperinsulinism (CH) is a severe disorder characterised by the appearance of severe hypoglycaemia. Pathogenic mutations in the ABCC8…”
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Congenital hyperinsulinism in Gran Canaria, Canary Isles by Nóvoa Medina, Yeray, Domínguez García, Ángela, Quinteiro González, Sofía, García Cruz, Loida María, Santana Rodríguez, Alfredo

“…Congenital hyperinsulinism (CH) is a severe disorder characterised by the appearance of severe hypoglycaemia. Pathogenic mutations in the ABCC8 and KCNJ11…”
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Amiloidosis cardiaca por transtiretina causada por la mutación Val122Ile en homocigosis en varón de raza blanca by Marrero Negrín, Natalia, Medina Gil, José María, García Cruz, María Loida, Jiménez Cabrera, Francisco

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Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction by Amor-Salamanca, Almudena, Santana Rodríguez, Alfredo, Rasoul, Hazhee, Rodríguez-Palomares, José F, Moldovan, Oana, Hey, Thomas Morris, Delgado, María Gallego, Cuenca, David López, de Castro Campos, Daniel, Basurte-Elorz, María Teresa, Macías-Ruiz, Rosa, Fuentes Cañamero, María Eugenia, Galvin, Joseph, Bilbao Quesada, Raquel, de la Higuera Romero, Luis, Trujillo-Quintero, Juan Pablo, García-Cruz, Loida María, Cárdenas-Reyes, Ivonne, Jiménez-Jáimez, Juan, García-Hernández, Soledad, Valverde-Gómez, María, Gómez-Díaz, Iria, Limeres Freire, Javier, García-Pinilla, José M, Gimeno-Blanes, Juan R, Savattis, Kostantinos, García-Pavía, Pablo, Ochoa, Juan Pablo

“…Less than 40% of patients with dilated cardiomyopathy (DCM) have a pathogenic/likely pathogenic genetic variant identified. has been linked to congenital heart…”
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Transthyretin Cardiac Amyloidosis Due to Homozygous Val122Ile Mutation in a Caucasian Man by Marrero Negrín, Natalia, Medina Gil, José María, García Cruz, María Loida, Jiménez Cabrera, Francisco

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