Zobrazeno 1 - 10
of 967
pro vyhledávání: '"Liena"'
Autor:
Maha Dahawi, Jean-Madeleine de Sainte Agathe, Mohamed S. Elmagzoub, Elhami A. Ahmed, Julien Buratti, Thomas Courtin, Eric Noé, Julie Bogoin, Bruno Copin, Fatima A. Elmugadam, Wasma A. Abdelgadir, Ahmed K. M. A. Ahmed, Mohamed A. Daldoum, Rayan Mamoon Ibrahim Altayeb, Mohamed Bashir, Leena Mohamed Khalid, Sahar Gamil, Sara Baldassari, Liena Elsayed, Boris Keren, Gregory Nuel, Ammar E. Ahmed, Eric Leguern
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-18 (2024)
Abstract Genetic generalized epilepsy (GGE) including childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy (JME), and GGE with tonic–clonic seizures (TCS) (GGE-TCS), is genetically influenced with a two- to four- fold
Externí odkaz:
https://doaj.org/article/da14490885db477eb26406082e9daf33
Autor:
Liena Elbaghir Omer Elsayed, Norah Ayed AlHarbi, Ashwaq Mohammed Alqarni, Huda Hussein Elwasila Eltayeb, Noura Mostafa Mohamed Mostafa, Maha Mohammed Abdulrahim, Hadeel Ibrahim Bin Zaid, Latifah Mansour Alanzi, Sarah Abdullah Ababtain, Khawlah Aldulaijan, Sheka Yagub Aloyouni, Moneeb Abdullah Kassem Othman, Mohammad Abdullah Alkheilewi, Adel Mohammed Binduraihem, Hadeel Abdollah Alrukban, Hiba Yousif Ahmed, Faten Abdullah AlRadini, Hadil Mohammad Alahdal, Aziza Mufareh Mushiba, Omaima Abdulazeem Alzaher
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-10 (2024)
Abstract Background Chromosome 16p11.2 deletions and duplications were found to be the second most common copy number variation (CNV) reported in cases with clinical presentation suggestive of chromosomal syndromes. Chromosome 16p11.2 deletion syndro
Externí odkaz:
https://doaj.org/article/c35507dced82439484a71711a4834fd0
Autor:
Liena Martina Bravo Urquiza, Marcelo Andia Kohnenkampf, Raquel Bridi, Juan Esteban Oyarzun Isamitt
Publikováno v:
Annals of Hepatology, Vol 29, Iss , Pp 101706- (2024)
Conflict of interest: No Introduction and Objectives: The increase in caloric intake has led to an obesity epidemic both in Chile and worldwide. This trend has contributed to a rise in the prevalence of metabolic diseases, such as insulin resistance,
Externí odkaz:
https://doaj.org/article/03a0e5e062b74e4781a149f219c0d90b
Autor:
Liena Elbaghir Omer Elsayed, Norah Ayed AlHarbi, Ashwaq Mohammed Alqarni, Huda Hussein Elwasila Eltayeb, Noura Mostafa Mohamed Mostafa, Maha Mohammed Abdulrahim, Hadeel Ibrahim Bin Zaid, Latifah Mansour Alanzi, Sarah Abdullah Ababtain, Khawlah Aldulaijan, Sheka Yagub Aloyouni, Moneeb Abdullah Kassem Othman, Mohammad Abdullah Alkheilewi, Adel Mohammed Binduraihem, Hadeel Abdollah Alrukban, Hiba Yousif Ahmed, Faten Abdullah AlRadini, Hadil Mohammad Alahdal, Aziza Mufareh Mushiba, Omaima Abdulazeem Alzaher
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/e24a3331985f49f8bdc8961b2c06b84b
Publikováno v:
Islas, Vol 66, Iss 208, Pp e1428-e1428 (2024)
Introducción: Los actuales sitios de redes sociales en Internet validan la teoría clásica de las redes sociales y los estudios sobre las audiencias que nacieron a inicios del pasado siglo. La nueva sociabilidad que surge en estas plataformas const
Externí odkaz:
https://doaj.org/article/9a06655b15d64611a16b2048480878e4
Autor:
Liena Hačatrjana, Dace Namsone
Publikováno v:
Journal of Intelligence, Vol 12, Iss 11, p 109 (2024)
Various skills related to critical thinking, reasoning, and scientific reasoning are defined as essential for students in policy documents and curricula around the world as essential both in school and in everyday life. However, these concepts are of
Externí odkaz:
https://doaj.org/article/20689820ce9242a98441eabf2bbe786e
Publikováno v:
Medisan, Vol 28, Iss 2, Pp e4847-e4847 (2024)
Introducción: El cáncer cervicouterino ocupa el tercer lugar como causa de defunción por neoplasias malignas a nivel mundial, afectando principalmente a los países de ingresos bajos y medianos. Hacia el 2020 se estimó una incidencia de 604 000 n
Externí odkaz:
https://doaj.org/article/edd2ddd76e8a4d10b7a52ea41f8bbaba
Autor:
Hillary Fernández-Gil-de-Montes, Amaurys Batista-Pérez, Liena Gainza-Pupo, Brunilda de los Ángeles Abeleira-Ortiz
Publikováno v:
Revista Electrónica Dr. Zoilo E. Marinello Vidaurreta, Vol 49, Iss 1, Pp e3690-e3690 (2024)
Background: diabetic retinopathy and diabetic kidney disease are highly feared microvascular complications. In our province, there are insufficient studies that address the possible association between these comorbidities. Objective: to characterize
Externí odkaz:
https://doaj.org/article/7ca2cbfd4d404d3ab920787259b6b75d
Autor:
Yousuf Bakhit, Christelle Tesson, Mohamed O. Ibrahim, Khalid Eltom, Isra Eltazi, Liena E.O. Elsayed, Suzanne Lesage, Osheik Seidi, Jean‐Christophe Corvol, Ullrich Wüllner, Sudanese Parkinson's Disease Study Group
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 6, Pp 983-989 (2023)
Abstract Introduction The phospholipase A2 group VI gene (PLA2G6) encodes an enzyme that catalyzes the hydrolytic release of fatty acids from phospholipids. Four neurological disorders with infantile, juvenile, or early adult‐onset are associated w
Externí odkaz:
https://doaj.org/article/f4451ea65aae4f268123131be8526103
Autor:
Mutaz Amin, Cedric Vignal, Esraa Eltaraifee, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed, Arwa Babai, Iman Elbadi, Doua Mustafa, Rayan Abubaker, Mohamed Mustafa, Severine Drunat, Liena E. O. Elsayed, Ammar E. Ahmed, Odile Boespflug-Tanguy, Imen Dorboz
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-5 (2022)
Abstract Background The etiology of intellectual disabilities is diverse and includes both genetic and environmental factors. The genetic causes of intellectual disabilities range from chromosomal aberrations to single gene disorders. The TRAPPC9 gen
Externí odkaz:
https://doaj.org/article/f46e6638b38a4340af6381da3127577b