Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Francisco, Arrieta"'
Autor:
Beatriz Ugalde-Abiega, Sinziana Stanescu, Amaya Belanger, Mercedes Martinez-Pardo, Francisco Arrieta
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-5 (2023)
Abstract Background Phenylketonuria (PKU) is an autosomal recessive disease that belongs to a group of disorders resulting from inborn errors of protein metabolism. It was the first disease included in neonatal screening. Neonatal screening has allow
Externí odkaz:
https://doaj.org/article/7f121f29c9fa4911ba5856795e407c10
Autor:
Teresa Vilariño-García, María L. Polonio-González, Antonio Pérez-Pérez, Josep Ribalta, Francisco Arrieta, Manuel Aguilar, Juan C. Obaya, José A. Gimeno-Orna, Pedro Iglesias, Jorge Navarro, Santiago Durán, Juan Pedro-Botet, Víctor Sánchez-Margalet
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 4, p 2338 (2024)
Diabetes mellitus (DM) is a highly prevalent disease worldwide, estimated to affect 1 in every 11 adults; among them, 90–95% of cases are type 2 diabetes mellitus. This is partly attributed to the surge in the prevalence of obesity, which has reach
Externí odkaz:
https://doaj.org/article/4f1f0436e09f4ba6bdb44c2397cb0e10
Autor:
Sinziana Stanescu, Irene Bravo-Alonso, Amaya Belanger-Quintana, Belen Pérez, Montserrat Medina-Diaz, Pedro Ruiz-Sala, Nathaly Paola Flores, Raquel Buenache, Francisco Arrieta, Pilar Rodríguez-Pombo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Monocarboxylate transporter 1 (MCT1) deficiency has recently been described as a rare cause of recurrent ketosis, the result of impaired ketone utilization in extrahepatic tissues. To date, only six patients with this condition ha
Externí odkaz:
https://doaj.org/article/bf838d3290344e92b33a55b04e45428f
Autor:
Sinziana Stanescu, Amaya Belanger-Quintana, Borja Manuel Fernandez-Felix, Francisco Arrieta, Victor Quintero, Maria Soledad Maldonado, Patricia Alcaide, Mercedes Martínez-Pardo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Abstract Background Propionic acidemia (PA), an inborn error of metabolism, is caused by a deficiency in propionyl-CoA carboxylase. Patients have to follow a diet restricted in the propiogenic amino acids isoleucine (Ile), valine (Val), methionine (M
Externí odkaz:
https://doaj.org/article/c21f6ba11f434c0e8b9358b24f8caf7d
Identification and Functional Analysis of APOB Variants in a Cohort of Hypercholesterolemic Patients
Autor:
Carmen Rodríguez-Jiménez, Gema de la Peña, Javier Sanguino, Sara Poyatos-Peláez, Ana Carazo, Pedro L. Martínez-Hernández, Francisco Arrieta, José M. Mostaza, Diego Gómez-Coronado, Sonia Rodríguez-Nóvoa
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 8, p 7635 (2023)
Mutations in APOB are the second most frequent cause of familial hypercholesterolemia (FH). APOB is highly polymorphic, and many variants are benign or of uncertain significance, so functional analysis is necessary to ascertain their pathogenicity. O
Externí odkaz:
https://doaj.org/article/d434e3f6e94c4196836edcbbae7858de
Autor:
Carolina Luque Calvo, Ángel Luis Mataix Sanjuan, Ángel Candela Toha, Nilda Martínez Castro, María Rosario Pintor Recuenco, José Luis Calleja López, José Ignacio Botella-Carretero, Francisco Arrieta Blanco
Publikováno v:
Nutrients, Vol 14, Iss 19, p 3892 (2022)
We aimed to analyse the impact of COVID-19 during 2020 and 2021 on the prescription of enteral nutritional support and its expenditure in the Community of Madrid, Spain, compared to pre-pandemic data from 2016 in the general population vs. elderly. W
Externí odkaz:
https://doaj.org/article/2b955d63726248cd80a4f1fe4c312857
Autor:
Sinziana Stanescu, Amaya Belanger-Quintana, Borja Manuel Fernández-Felix, Pedro Ruiz-Sala, Patricia Alcaide, Francisco Arrieta, Mercedes Martínez-Pardo
Publikováno v:
Antioxidants, Vol 11, Iss 8, p 1588 (2022)
Propionic acidaemia (PA) is an innate error of metabolism involving a deficiency in the enzyme propionyl-CoA carboxylase. Better control of acute decompensation episodes together with better treatment and monitoring have improved the prognosis of pat
Externí odkaz:
https://doaj.org/article/c63033fcc092491d91ac65c6d3af9b80
Autor:
Aura D. Herrera-Martínez, Sonia Junquera-Bañares, Lucía Turrión-Merino, Francisco Arrieta-Blanco, José Botella-Carretero, Clotilde Vázquez-Martínez, Alfonso Calañas-Continente
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Bariatric surgery is one of the most effective treatments currently available for obesity and its derived comorbidities. However, complications may occur, especially when malabsorptive surgeries like a biliopancreatic diversion is performed. We prese
Externí odkaz:
https://doaj.org/article/7af5962376374ed193b763bb7441f3aa
Autor:
Amaya Bélanger-Quintana, Francisco Arrieta Blanco, Delia Barrio-Carreras, Ana Bergua Martínez, Elvira Cañedo Villarroya, María Teresa García-Silva, Rosa Lama More, Elena Martín-Hernández, Ana Moráis López, Montserrat Morales-Conejo, Consuelo Pedrón-Giner, Pilar Quijada-Fraile, Sinziana Stanescu, Mercedes Martínez-Pardo Casanova
Publikováno v:
Nutrients, Vol 14, Iss 13, p 2755 (2022)
Hyperammonaemia is a metabolic derangement that may cause severe neurological damage and even death due to cerebral oedema, further complicating the prognosis of its triggering disease. In small children it is a rare condition usually associated to i
Externí odkaz:
https://doaj.org/article/368d2091b20549cbbd0c1641d671d970
Autor:
Juan, Pedro-Botet, Vivencio, Barrios, Víctor, Sánchez-Margalet, Juan, Tamargo, Francisco, Arrieta, José Mª, Gámez, José Antonio, Gimeno-Orna, Carlos, Escobar, Juan José, Gómez-Doblas, Antonio, Pérez
Publikováno v:
Endocrinología, Diabetes y Nutrición (English ed.). 70:51-62
The Working Groups of Cardiovascular Pharmacotherapy of the Sociedad Española de Cardiología and Cardiovascular Disease of the Sociedad Española de Diabetes have prepared a consensus document on the treatment of hypertriglyceridaemia in patients w