Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Claudia, Barletta Carrillo"'
Autor:
Miguel Hueda-Zavaleta, Juan Carlos Gomez de la Torre, Diana Minchón-Vizconde, Claudia Barletta-Carrillo, Cesar Copaja-Corzo, Gustavo Tapia-Sequeiros, Cinthya Flores, Cristian Piscoche, Cecilia Miranda, Ada Mendoza, Vicente A. Benites-Zapata
Publikováno v:
Therapeutic Advances in Infectious Disease, Vol 11 (2024)
Background: Molecular tests have contributed to reducing the mortality rate through early and accurate diagnosis of tuberculosis (TB). This is due to their low processing complexity and diagnostic accuracy superior to conventional methods. Objective:
Externí odkaz:
https://doaj.org/article/c02a166af7094e8a9a7d5d07e0adb847
Autor:
Miguel Hueda-Zavaleta, Juan Gomez-de-la-Torre, Claudia Barletta-Carrillo, Cinthya Flores-Flores, Nilver Piscoche-Botello, Cecilia Miranda-Visalot, Ada Mendoza-Farro, Sujey Gomez-Colque, Álvaro Taype-Rondán, Cesar Copaja-Corzo
Publikováno v:
Clinical Epidemiology and Global Health, Vol 29, Iss , Pp 101730- (2024)
Background: Tuberculosis (TB) is one of the leading causes of death worldwide. However, an accurate diagnosis contributes to timely treatment, reducing its adverse consequences. The aim of this research was to determine the diagnostic accuracy of the
Externí odkaz:
https://doaj.org/article/cc8aa5b6b50b4dc5b98b2a4eba7a527a
Autor:
Hugo Hernán Abarca Barriga, Felix Chavesta Velásquez, Claudia Barletta Carrillo, Abel Paucarmayta Tacuri, Margaret Bazán Hurtado, Tania Vásquez Loarte, Luis Ordoñez Rondón, Marco Ordoñez Linares, Evelina Andrea Rondón Abuhadba
Publikováno v:
Revista de la Facultad de Ciencias Médicas de Córdoba, Vol 79, Iss 2 (2022)
Introducción. Las variantes en el número de copias son un tipo de cambios en el genoma provocan anomalías congénitas. Objetivo. Determinar las variantes en el número de copias y el grado de consanguinidad parental en neonatos con síndromes m
Externí odkaz:
https://doaj.org/article/76eb4748d2b54839a69ec336c9daa275
Autor:
Juan Carlos Gómez de la Torre Pretell, Miguel Hueda-Zavaleta, José Alonso Cáceres-DelAguila, Claudia Barletta-Carrillo, Cesar Copaja-Corzo, Maria del Pilar Suarez Poccorpachi, María Soledad Vega Delgado, Gloria Maria Magdalena Levano Sanchez, Vicente A. Benites-Zapata
Publikováno v:
Tropical Medicine and Infectious Disease, Vol 7, Iss 11, p 340 (2022)
The COVID-19 pandemic circumstances have varied the pathogens related to acute respiratory infections (ARI), and most specialists have ignored them due to SARS-CoV-2’s similar symptomatology. We identify respiratory pathogens with multiplex PCR in
Externí odkaz:
https://doaj.org/article/cbbd1df0f7ef4eb7a953b46f3cf9117a
Autor:
María del Carmen Castro-Mujica, Claudia Barletta-Carrillo, Julio A. Poterico, Marisa Acosta, Jesús Valer, Miguel De La Cruz
Publikováno v:
Revista Peruana de Medicina Experimental y Salud Pública, Vol 34, Iss 4, Pp 744-50 (2017)
El síndrome Gorlin (SG) es una condición genética, con patrón de herencia autosómico dominante, con penetrancia completa y expresividad variable, debida a mutaciones germinales en los genes PTCH1 o SUFU, los cuales son componentes de la vía mol
Externí odkaz:
https://doaj.org/article/8f5fce7abd6143eb97f473aacbd56de3
Autor:
Benedito Mauro Rossi, Edenir Inêz Palmero, Francisco López-Kostner, Carlos Sarroca, Carlos Alberto Vaccaro, Florencia Spirandelli, Patricia Ashton-Prolla, Yenni Rodriguez, Henrique de Campos Reis Galvão, Rui Manuel Reis, André Escremim de Paula, Luis Gustavo Capochin Romagnolo, Karin Alvarez, Adriana Della Valle, Florencia Neffa, Pablo German Kalfayan, Enrique Spirandelli, Sergio Chialina, Melva Gutiérrez Angulo, Maria del Carmen Castro-Mujica, Julio Sanchez de Monte, Richard Quispe, Sabrina Daniela da Silva, Norma Teresa Rossi, Claudia Barletta-Carrillo, Susana Revollo, Ximena Taborga, L. Lena Morillas, Hélène Tubeuf, Erika Maria Monteiro-Santos, Tamara Alejandra Piñero, Constantino Dominguez-Barrera, Patrik Wernhoff, Alexandra Martins, Eivind Hovig, Pål Møller, Mev Dominguez-Valentin
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-26 (2017)
Abstract Background Genetic counselling and testing for Lynch syndrome (LS) have recently been introduced in several Latin America countries. We aimed to characterize the clinical, molecular and mismatch repair (MMR) variants spectrum of patients wit
Externí odkaz:
https://doaj.org/article/1c493e85a2f64dbc8249789857b5f939
Autor:
Hugo Hernán, Abarca Barriga, Felix, Chavesta Velásquez, Claudia, Barletta Carrillo, Abel, Paucarmayta Tacuri, Margaret, Bazán Hurtado, Tania, Vásquez Loarte, Luis, Ordoñez Rondón, Marco, Ordoñez Linares, Evelina Andrea, Rondón Abuhadba
Publikováno v:
Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina). 79(2)
Congenital abnormalities could be caused by copy number variation or homozygous variants inherited of parental consanguineous. Purpose.To show copy number variants and regions of homozygosity in neonates with malformative syndrome or one congenital a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f274c90686cf6aa50c8635d51df7d2e
https://pubmed.ncbi.nlm.nih.gov/35700460
https://pubmed.ncbi.nlm.nih.gov/35700460
Autor:
Leonor Gusmão, Bruce Budowle, Carlos Vullo, Jennifer Churchill Cihlar, Reinhard Würzner, Seah Lay Hong, Claudia Barletta-Carrillo, Wiliam Usaquén, Bettina Zimmermann, Rosane Silva, Chantal Roth, Martin Bodner, Harald Niederstätter, Rodrigo S. Moura-Neto, L. Souto, Gabriela Huber, Robert Lagacé, Dayse A. Silva, Christina Strobl, Balázs Egyed, Walther Parson, Dean Herman Tineo, Andrea Casas-Vargas, Catarina Xavier, Katja Anslinger, Farida Alshamali, Lisa Schnaller, Sharon Wootton, Renata Jankova-Ajanovska, Nicole Huber
Publikováno v:
Forensic Science International: Genetics. 42:244-251
The emergence of Massively Parallel Sequencing technologies enabled the analysis of full mitochondrial (mt)DNA sequences from forensically relevant samples that have, so far, only been typed in the control region or its hypervariable segments. In thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a4bb1afd84e058de6c8131244b436d
https://doi.org/10.1016/j.fsigen.2019.07.013
https://doi.org/10.1016/j.fsigen.2019.07.013
Autor:
Claudia Barletta-Carrillo, Sandro Casavilca-Zambrano, María del Carmen Castro-Mujica, Julio A. Poterico
Publikováno v:
Revista M�dica del Hospital General de M�xico. 83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43b88577f5dc359755781c3ed393d8cd
https://doi.org/10.24875/hgmx.20000050
https://doi.org/10.24875/hgmx.20000050
Autor:
Félix Chavesta-Velásquez, Marco Edmundo Ordoñez-Linares, Milana Trubnykova, Claudia Barletta-Carrillo, Hugo Abarca-Barriga, Andrea Rondón-Abuhadba
Publikováno v:
J Pediatr Genet
Copy number variation in loss of 3p13 is an infrequently reported entity characterized by hypertelorism, aniridia, microphthalmia, high palate, neurosensorial deafness, camptodactyly, heart malformation, development delay, autism spectrum disorder, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5039003837beccbdbcd55b1f945e1dd8
https://europepmc.org/articles/PMC7396471/
https://europepmc.org/articles/PMC7396471/
