Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Alexandra, Perez"'
Autor:
Florencia Anunziata, Cynthia Cisneros, Maria Isabella Natale Castillo, Alexandra Perez, Valeria Rodriguez, Sheila De La Cruz, Karla Estrada, Abigaile Durbal, Mishaska Jaramillo, Lidia Enriquez Marquez, Janet Nuñez, Myriam Peralta-Carcelen, Jessica Lee Wisnowski
Publikováno v:
Developmental Cognitive Neuroscience, Vol 70, Iss , Pp 101477- (2024)
The HEALthy Brain and Child Development (HBCD) Study, a multi-site prospective longitudinal cohort study, will examine human brain, cognitive, behavioral, social, and emotional development beginning prenatally and planned through early childhood. Cen
Externí odkaz:
https://doaj.org/article/084b795cd2cd40b39d6ebb7772b86fc0
Autor:
Julie A. Kable, Alexandra S. Potter, Natacha Akshoomoff, Patricia M. Blasco, Stefanie Bodson, Lucia Ciciolla, Sherry DeGray, Zoe Hulce, Emily S. Kuschner, Britley Learnard, Monica Luciana, Alexandra Perez, Miriam A. Novack, Tracy Riggins, So Yeon Shin, Sidney Smith, Jennifer Vannest, Eric.H. Zimak
Publikováno v:
Developmental Cognitive Neuroscience, Vol 70, Iss , Pp 101461- (2024)
The HEALthy Brain and Child Development (HBCD) study, a multi-site prospective longitudinal cohort study, will examine human brain, cognitive, behavioral, social, and emotional development beginning prenatally and planned through early childhood. The
Externí odkaz:
https://doaj.org/article/851c05e1615f4087806859cd2e4c38d2
Publikováno v:
Rheumato, Vol 3, Iss 1, Pp 74-85 (2023)
Gout is one of the most common inflammatory conditions with a growing global prevalence. Individuals with gout are at higher risk of developing chronic conditions, such as diabetes, chronic kidney disease (CKD), and cardiovascular diseases. In this s
Externí odkaz:
https://doaj.org/article/1393191c85d149c8bf58531a97871a12
Autor:
Sergi Cesar, Monica Coll, Victoria Fiol, Anna Fernandez-Falgueras, Jose Cruzalegui, Anna Iglesias, Isaac Moll, Alexandra Perez-Serra, Estefanía Martínez-Barrios, Carles Ferrer-Costa, Bernat del Olmo, Marta Puigmulè, Mireia Alcalde, Laura Lopez, Ferran Pico, Rubén Berrueco, Josep Brugada, Irene Zschaeck, Daniel Natera-de Benito, Laura Carrera-García, Jessica Exposito-Escudero, Carlos Ortez, Andrés Nascimento, Ramon Brugada, Georgia Sarquella-Brugada, Oscar Campuzano
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Laminopathies are caused by rare alterations in LMNA, leading to a wide clinical spectrum. Though muscular dystrophy begins at early ages, disease progression is different in each patient. We investigated variability in laminopathy phenot
Externí odkaz:
https://doaj.org/article/2e963c1eaf3740048e1406c93f7e7001
Akademický článek
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Publikováno v:
Journal of Pain & Palliative Care Pharmacotherapy. :1-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acb77c88a894304edbcc851f28131718
https://doi.org/10.1080/15360288.2023.2194868
https://doi.org/10.1080/15360288.2023.2194868
Autor:
Spencer S. Liem, Timothy Demus, Alexandra Perez, Dhaval Jivanji, Crystal Y. Lee, Kevin A. George, Alejandra Perez, Luigi Cubeddu, Jorge F. Pereira
Publikováno v:
International Urology and Nephrology. 55:1109-1116
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baaa5b800f6b1cae1a788fcf25c04f0e
https://doi.org/10.1007/s11255-023-03545-w
https://doi.org/10.1007/s11255-023-03545-w
Autor:
Estefanía Martinez-Barrios, Georgia Sarquella-Brugada, Alexandra Perez-Serra, Anna Fernandez-Falgueras, Sergi Cesar, Mireia Alcalde, Mónica Coll, Marta Puigmulé, Anna Iglesias, Carles Ferrer-Costa, Bernat del Olmo, Ferran Picó, Laura Lopez, Victoria Fiol, José Cruzalegui, Clara Hernandez, Elena Arbelo, Nuria Díez-Escuté, Patricia Cerralbo, Simone Grassi, Antonio Oliva, Rocío Toro, Josep Brugada, Ramon Brugada, Oscar Campuzano
Publikováno v:
International Journal of Legal Medicine. 137:345-351
Sudden death cases in the young population remain without a conclusive cause of decease in almost 40% of cases. In these situations, cardiac arrhythmia of genetic origin is suspected as the most plausible cause of death. Molecular autopsy may reveal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17eeef65ef3b1beda2e4f99a783bb000
https://doi.org/10.1007/s00414-023-02951-0
https://doi.org/10.1007/s00414-023-02951-0
Publikováno v:
Genes and Diseases, Vol 3, Iss 4, Pp 257-262 (2016)
Atrial fibrillation is the most common sustained arrhythmia and remains as one of main challenges in current clinical practice. The disease may be induced secondary to other diseases such as hypertension, valvular heart disease, and heart failure, co
Externí odkaz:
https://doaj.org/article/3cd839f839b54ee487e42e3d68cdb6e0
Autor:
Oscar Campuzano, Anna Fernandez-Falgueras, Georgia Sarquella-Brugada, Sergi Cesar, Elena Arbelo, Ana García-Álvarez, Paloma Jordà, Monica Coll, Victoria Fiol, Anna Iglesias, Alexandra Perez-Serra, Jesus Mates, Bernat del Olmo, Carles Ferrer, Mireia Alcalde, Marta Puigmulé, Irene Mademont-Soler, Ferran Pico, Laura Lopez, Coloma Tiron, Josep Brugada, Ramon Brugada
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Cardiomyopathies are a heterogeneous group of inherited cardiac diseases characterized by progressive myocardium abnormalities associated with mechanical and/or electrical dysfunction. Massive genetic sequencing technologies allow a comprehensive gen
Externí odkaz:
https://doaj.org/article/c52142240d0240338c8956657072679f