Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Maria Teresa Tusié"'
Autor:
David Z. Pan, Zong Miao, Caroline Comenho, Sandhya Rajkumar, Amogha Koka, Seung Hyuk T. Lee, Marcus Alvarez, Dorota Kaminska, Arthur Ko, Janet S. Sinsheimer, Karen L. Mohlke, Nicholas Mancuso, Linda Liliana Muñoz-Hernandez, Miguel Herrera-Hernandez, Maria Teresa Tusié-Luna, Carlos Aguilar-Salinas, Kirsi H. Pietiläinen, Jussi Pihlajamäki, Markku Laakso, Kristina M. Garske, Päivi Pajukanta
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-20 (2021)
Abstract Background Obesity predisposes individuals to multiple cardiometabolic disorders, including type 2 diabetes (T2D). As body mass index (BMI) cannot reliably differentiate fat from lean mass, the metabolically detrimental abdominal obesity has
Externí odkaz:
https://doaj.org/article/a78b7b24f81c435489080bb179d2de77
Autor:
Roopa Mehta, Daniel Elías-López, Alexandro J. Martagón, Oscar A Pérez-Méndez, Maria Luisa Ordóñez Sánchez, Yayoi Segura, Maria Teresa Tusié, Carlos A. Aguilar-Salinas
Publikováno v:
Lipids in Health and Disease, Vol 20, Iss 1, Pp 1-18 (2021)
Abstract Background LCAT (lecithin-cholesterol acyltransferase) deficiency is characterized by two distinct phenotypes, familial LCAT deficiency (FLD) and Fish Eye disease (FED). This is the first systematic review evaluating the ethnic distribution
Externí odkaz:
https://doaj.org/article/e7975c1e05f647299d4cd386334baa52
Autor:
David Z. Pan, Zong Miao, Caroline Comenho, Sandhya Rajkumar, Amogha Koka, Seung Hyuk T. Lee, Marcus Alvarez, Dorota Kaminska, Arthur Ko, Janet S. Sinsheimer, Karen L. Mohlke, Nicholas Mancuso, Linda Liliana Muñoz-Hernandez, Miguel Herrera-Hernandez, Maria Teresa Tusié-Luna, Carlos Aguilar-Salinas, Kirsi H. Pietiläinen, Jussi Pihlajamäki, Markku Laakso, Kristina M. Garske, Päivi Pajukanta
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/732d3f0d3a334be5a5f29139e9ab4c14
Akademický článek
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Autor:
Maria Teresa Tusié, Carlos A. Aguilar-Salinas, Daniel Elías-López, Maria Luisa Ordóñez Sánchez, Yayoi Segura, Roopa Mehta, Alexandro J. Martagón, Oscar Pérez-Méndez
Publikováno v:
Lipids in Health and Disease, Vol 20, Iss 1, Pp 1-18 (2021)
Lipids in Health and Disease
Lipids in Health and Disease
Background LCAT (lecithin-cholesterol acyltransferase) deficiency is characterized by two distinct phenotypes, familial LCAT deficiency (FLD) and Fish Eye disease (FED). This is the first systematic review evaluating the ethnic distribution of LCAT d
Autor:
Carlos A. Aguilar-Salinas, Roopa Mehta, Oscar Pérez-Méndez, María Luisa Ordóñez-Sánchez, Yayoi Segura, Daniel Elías-López, Alexandro J. Martagón, Maria Teresa Tusié
Background: LCAT deficiency is a rare disease, characterized by two distinct phenotypes, familial LCAT deficiency (FLD) and Fish Eye disease (FED). There is little knowledge of LCAT deficiency syndromes in Amerindian populations. We present the resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96b1f7b8a98bca3d8c5b4039398540fa
https://doi.org/10.21203/rs.3.rs-97455/v1
https://doi.org/10.21203/rs.3.rs-97455/v1
Autor:
César Ernesto, Lam-Chung, Álvaro, Elizondo Ochoa, Yayoi, Segura Kato, Juanita, Silva-Serrano, María Teresa, Tusié Luna, Almeda-Valdes, Paloma
Publikováno v:
In AACE Clinical Case Reports March-April 2021 7(2):138-140
Autor:
Dalia Cuenca, Jose Luis Ventura-Gallegos, Paloma Almeda-Valdes, María Teresa Tusié-Luna, Alfredo Reza-Albarran, Laura Ventura-Ayala, Ma. Luisa Ordoñez-Sánchez, Yayoi Segura-Kato, Francisco Javier Gomez-Perez, Michelle De Puy Conte, Lizbet Ruilova Gonzalez, Alejandro Zentella-Dehesa
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 35, Iss , Pp 100965- (2023)
Severe insulin resistance can be caused by rare genetic defects in the insulin receptor known as insulin receptoropathies. These genetic defects cause a wide spectrum of clinical manifestations ranging from mild syndromes to lethal disorders. Among t
Externí odkaz:
https://doaj.org/article/54dc240e5dbb40a293e3a8ce3a47ce6c
Autor:
Ivette Cruz-Bautista, Alicia Huerta-Chagoya, Hortensia Moreno-Macías, Rosario Rodríguez-Guillén, María Luisa Ordóñez-Sánchez, Yayoi Segura-Kato, Roopa Mehta, Paloma Almeda-Valdés, Lizeth Gómez-Munguía, Ximena Ruiz-De Chávez, Ximena Rosas-Flota, Arali Andrade-Amado, Bárbara Bernal-Barroeta, María Guadalupe López-Carrasco, Luz Elizabeth Guillén-Pineda, Angelina López-Estrada, Daniel Elías-López, Alexandro J. Martagón-Rosado, Donají Gómez-Velasco, Cesar Ernesto Lam-Chung, Omar Yaxmehen Bello-Chavolla, Fabiola Del Razo-Olvera, Lucely D. Cetina-Pérez, José Luis Acosta-Rodríguez, María Teresa Tusié-Luna, Carlos A. Aguilar-Salinas
Publikováno v:
Lipids in Health and Disease, Vol 20, Iss 1, Pp 1-13 (2021)
Abstract Background Familial hypertriglyceridemia (FHTG) is a partially characterized primary dyslipidemia which is frequently confused with other forms hypertriglyceridemia. The aim of this work is to search for specific features that can help physi
Externí odkaz:
https://doaj.org/article/65d5c8711dd447cab13487fcecca3748
Autor:
Aarón, Domínguez-López, Angel, Miliar-García, Yayoi X, Segura-Kato, Laura, Riba, Riba, Esparza-López, Salvador, Ramírez-Jiménez, Maribel, Rodríguez-Torres, Samuel, Canizales-Quinteros, Siraam, Cabrera-Vásquez, Verónica, Fragoso-Ontiveros, Carlos A, Aguilar-Salinas, Nelly, Altamirano-Bustamante, Raúl, Calzada-León, Carlos, Robles-Valdés, Luz E, Bravo-Ríos, Maria Teresa, Tusié-Luna
Publikováno v:
JOP : Journal of the pancreas. 6(3)
Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes mellitus characterized by autosomal dominant inheritance, early age of onset and a primary insulin secretion defect. Certain MODY gene sequence variants may be involved in po